Method for promoting plant growth
Granted 20 Feb 2018 · 3 office actions
Assignee: Sumitomo Chemical
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Attorney: Attorney · Log in to unlock
Inventors: Fujio Mukumoto, Hiroaki Tamaki, Mitsuhiko Iwakoshi, Shintaro Kusaka · Examiner: Robert A Wax · AU 1616 · TC 1600
Life of the application
13 dated eventsDescription
80 parts›TECHNICAL FIELD
The present invention relates to a method for promoting plant growth.
›BACKGROUND ART
Some chemical substances are known to exert an effect of promoting plant growth by being applied to plants. For example, when aminolevulinic acid is applied to plants, this substance exerts an effect of promoting growth of the plants.
›RELATED ART DOCUMENT
Non-Patent Document
Non-Patent Document-1: <Biosynthesis, biotechnological production and applications of 5-aminolevulinic acid> K. Sasaki et al., (2002) Applied Microbiology and Biotechnology 58: pp 23-29
›DISCLOSURE OF THE INVENTION · 1 of 4
Objects of the present invention are to provide a method or the like that excellently promotes plant growth.
As a result of intensive studies, the present inventors found out that the application of a certain compound to plants promotes growth of the plants and have therefore completed the present invention.
That is, the present invention is as follows.
[1] A method for promoting plant growth, which comprises treating a plant with a compound represented by the following Formula (1):
wherein
W represents —OR 6 , —ON═CR 7 R 8 , —SR 9 , or —NR 7 R 10 ,
R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from a group X, a C2-C6 alkenyl group optionally having one or more groups selected from the group X, a C2-C6 alkynyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from a group Y, a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a carboxy group, a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, an aminocarbonyl group, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 11 , —S(O) m R 11 , or —SF 5 ,
R 2 represents a hydrogen atom, a halogen atom, a cyano group, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a C2-C6 alkenyl group optionally having one or more groups selected from the group X, a C2-C6 alkynyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a carboxy group, a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, an aminocarbonyl group, —NR 12 R 13 , —S(O) 2 NR 7 R 11 , —OR 13 , —S(O) m R 13 , or —SF 5 ,
R 3 and R 4 are the same or different and each represents a hydrogen atom, a halogen atom, a cyano group, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a C2-C6 alkenyl group optionally having one or more groups selected from the group X, a C2-C6 alkynyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a carboxy group, a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, an aminocarbonyl group, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 11 , —S(O) m R 11 , or —SF 5 ,
R 5 represents a hydrogen atom, a halogen atom, a cyano group, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a carboxy group, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 14 , a phenyl group optionally having one or more groups selected from the group Y, a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, or a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y,
R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from a group Z, a C3-C6 alkenyl group optionally having one or more groups selected from the group X, a C3-C6 alkynyl group optionally having one or more groups selected from the group X, a C4-C7 cycloalkylalkyl group optionally having one or more halogen atoms, a C3-C6 cycloalkyl group optionally having one or more halogen atoms, a phenyl group optionally having one or more groups selected from the group Y, or a C7-C9 phenylalkyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y,
R 7 and R 8 are the same or different and each represents a C1-C6 alkyl group optionally having one or more halogen atoms, a phenyl group optionally having one or more groups selected from the group Y, or a hydrogen atom,
R 9 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, a C3-C6 alkenyl group optionally having one or more groups selected from the group X, a C3-C6 alkynyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, or a C7-C9 phenylalkyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y,
R 10 represents a hydrogen atom, a cyano group, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, a phenyl group optionally having one or more groups selected from the group Y, a benzyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y, —OR 7 , or —NR 7 R 8 ,
R 11 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, a C3-C6 alkenyl group optionally having one or more groups selected from the group X, a C3-C6 alkynyl group optionally having one or more groups selected from the group X, a C4-C7 cycloalkylalkyl group optionally having one or more halogen atoms, a C7-C9 phenylalkyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y, a 6-membered aromatic heterocyclic-C1-C3 alkyl group wherein a 6-membered aromatic heterocyclic portion may have optionally one or more groups selected from the group Y, a phenyl group optionally having one or more groups selected from the group Y, a C3-C6 cycloalkyl group optionally having one or more halogen atoms, or a hydrogen atom (provided that when m in —S(O) m R 11 is 1 or 2, R 11 is not a hydrogen atom),
›DISCLOSURE OF THE INVENTION · 2 of 4
R 12 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C1-C4 alkylsulfonyl group optionally having one or more halogen atoms, a phenylsulfonyl group optionally having one or more groups selected from the group Y, a C7-C9 phenylalkylsulfonyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —C(O)R 15 , or —C(O)NR 7 R 8 ,
R 13 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, a C3-C6 alkenyl group optionally having one or more groups selected from the group X, a C3-C6 alkynyl group optionally having one or more groups selected from the group X, a C4-C7 cycloalkylalkyl group optionally having one or more halogen atoms, a C3-C6 cycloalkyl group optionally having one or more halogen atoms, a C7-C9 phenylalkyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y, or a hydrogen atom (provided that when m in —S(O) m R 13 is 1 or 2, R 13 is not a hydrogen atom),
R 14 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, a C3-C6 alkenyl group optionally having one or more groups selected from the group X, a C3-C6 alkynyl group optionally having one or more groups selected from the group X, a C4-C7 cycloalkylalkyl group optionally having one or more halogen atoms, a C3-C6 cycloalkyl group optionally having one or more halogen atoms, a C7-C9 phenylalkyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a C1-C6 alkylsulfonyl group optionally having one or more halogen atoms, a phenylsulfonyl group optionally having one or more groups selected from the group Y, or a hydrogen atom,
R 15 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more halogen atoms, a phenyl group optionally having one or more groups selected from the group Y, a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, or a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and
m represents 0, 1, or 2,
the group X represents a group consisting of a halogen atom, a cyano group, and a C1-C6 alkoxy group optionally having one or more halogen atoms,
the group Y represents a group consisting of a halogen atom, a cyano group, a nitro group, a C1-C6 alkyl group optionally having one or more halogen atoms, and a C1-C6 alkoxy group optionally having one or more halogen atoms, and
the group Z represents a group consisting of a halogen atom, a hydroxy group, a C1-C6 alkoxy group optionally having one or more halogen atoms, and a C2-C6 alkoxycarbonyl group,
(hereinafter, described as a “compound of the present invention”),
provided that a method for promoting plant growth which comprises treating plants with a compound corresponding to any one of the following (1) to (8) is excluded,
(1) Methyl 4-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (2) Methyl 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (3) Methyl 6-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (4) Methyl 7-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (5) Ethyl 4-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (6) Ethyl 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (7) Ethyl 6-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, (8) Ethyl 7-(trifluoromethyl)benzo[b]thiophene-2-carboxylate.
[2] The method according to [1], in which the compound represented by Formula (1) is a compound wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a C2-C6 alkenyl group optionally having one or more groups selected from the group X, a C2-C6 alkynyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a carboxy group, a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, an aminocarbonyl croup, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 11 , —S(O) m R 11 , or —SF 5 ,
R 4 represents a hydrogen atom, a halogen atom, a cyano group, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a C2-C6 alkenyl group optionally having one or more groups selected from the group X, a C2-C6 alkynyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a carboxy group, a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, an aminocarbonyl group, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 11 , —S(O) m R 11 , or —SF 5 .
[3] The method according to [1], in which the compound represented by Formula (1) is a compound wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C4 alkyl group which may have optionally one or more halogen atoms, a C2-C4 alkenyl group optionally having one or more halogen atoms, a C2-C4 alkynyl group optionally having one or more halogen atoms, a phenyl group optionally having one or more groups selected from the group Y, a pyridyl group optionally having one or more groups selected from the group Y, a pyrimidinyl group optionally having one or more groups selected from the group Y, a thienyl group optionally having one or more groups selected from the group Y, a pyrrolyl group optionally having one or more groups selected from the group Y, a C2-C5 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a C2-C4 alkoxycarbonyl group, an aminocarbonyl group, —NR 11 R 12 , —OR 11 , —S(O) m R 11 , or —SF 5 ,
›DISCLOSURE OF THE INVENTION · 3 of 4
R 2 represents a hydrogen atom, a halogen atom, a cyano group, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C4 alkenyl group optionally having one or more halogen atoms, a C2-C4 alkynyl group optionally having one or more halogen atoms, a phenyl group optionally having one or more groups selected from the group Y, a pyridyl group optionally having one or more groups selected from the group Y, a pyrimidinyl group which may have optionally one or more groups selected from the group Y, a thienyl group optionally having one or more groups selected from the group Y, a pyrrolyl group optionally having one or more groups selected from the group Y, a C2-C5 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a C2-C4 alkoxycarbonyl group, an aminocarbonyl group, —NR 12 R 13 , —OR 13 , —S(O) m R 13 , or —SF 5 ,
R 3 and R 4 are the same or different and each represents a hydrogen atom, a halogen atom, a cyano group, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C4 alkenyl group optionally having one or more halogen atoms, a C2-C4 alkynyl group optionally having one or more halogen atoms, a phenyl group optionally having one or more groups selected from the group Y, a pyridyl group optionally having one or more groups selected from the group Y, a pyrimidinyl group optionally having one or more groups selected from the group Y, a thienyl group optionally having one or more groups selected from the group Y, a pyrrolyl group optionally having one or more groups selected from the group Y, a C2-C5 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a C2-C4 alkoxycarbonyl group, an aminocarbonyl group, —NR 11 R 12 , —OR 11 , —S(O) m R 11 , or —SF 5 ,
R 5 represents a hydrogen atom, a halogen atom, a cyano group, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C5 alkoxycarbonyl group, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y,
R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z, a C3-C6 alkenyl group optionally having one or more halogen atoms, a C3-C6 alkynyl group optionally having one or more halogen atoms, a phenyl group optionally having one or more groups selected from the group Y, or a C7-C9 phenylalkyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y,
R 7 and R 8 are the same or different and each represents a C1-C4 alkyl group optionally having one or more halogen atoms, a phenyl group optionally having one or more groups selected from the group Y, or a hydrogen atom,
R 9 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, a C3-C6 alkenyl group optionally having one or more halogen atoms, a C3-C6 alkynyl group optionally having one or more halogen atoms, a phenyl group optionally having one or more groups selected from the group Y, or a C7-C9 phenylalkyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y,
R 10 represents a hydrogen atom, a cyano group, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, a phenyl group optionally having one or more groups selected from the group Y, —OR 7 , or —NR 7 R 8 ,
R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, a C3-C4 alkynyl group optionally having one or more groups selected from the group X, a C7-C9 phenylalkyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y, a pyridyl-C1-C3 alkyl group wherein a pyridine ring portion may have optionally one or more groups selected from the group Y, a phenyl group optionally having one or more groups selected from the group Y, or a hydrogen atom (provided that when m in —S(O) m R 11 is 1 or 2, R 11 is not a hydrogen atom),
R 12 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C1-C4 alkylsulfonyl group optionally having one or more halogen atoms, a phenylsulfonyl group optionally having one or more groups selected from the group Y, a benzylsulfonyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y, —C(O)R 15 , or —C(O)NR 7 R 8 ,
R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms or a hydrogen atom (provided that when m in —S(O) m R 13 is 1 or 2, R 13 is not a hydrogen atom),
R 14 represents a C1-C4 alkyl group optionally having one or more groups selected from the group X, a C3-C6 alkenyl group optionally having one or more halogen atoms, a benzyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y, a phenyl group optionally having one or more groups selected from the group Y, a C2-C5 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a phenylsulfonyl group optionally having one or more groups selected from the group Y, or a hydrogen atom,
R 15 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a phenyl group optionally having one or more groups selected from the group Y, a thienyl group optionally having one or more groups selected from the group Y, a pyrazolyl group optionally having one or more groups selected from the group Y, or an isoxazolyl group optionally having one or more groups selected from the group Y.
[4] The method for promoting plant growth according to any one of [1] to [3], in which the plant is a plant that has been or will be exposed to abiotic stress.
[5] The method according to any one of [1] to [4], in which the application to the plant includes a spraying treatment, a soil treatment, a seed treatment, or a hydroponic treatment.
›DISCLOSURE OF THE INVENTION · 4 of 4
[6] The method according to any one of [1] to [4], in which the application to the plant is the seed treatment.
[7] The method according to any one of [1] to [6], in which the plant is rice, corn, or wheat.
[8] The method according to any one of [1] to [7], [15] or [16], in which the plant is a transgenic plant.
[9] The method according to any one of [4] to [8], [15] or [16], in which the abiotic stress is high-temperature stress.
[10] The method according to any one of [4] to [8], [15] or [16], in which the abiotic stress is low-temperature stress.
[11] The method according to any one of [4] to [8], [15] or [16], in which the abiotic stress is drought stress.
[12] Use of the compound represented the Formula (1) described in above [1] for promoting plant growth
[13] A plant seed which is obtained by being treated with the compound represented by the Formula (1) described in above [1] in an effective dose,
[14] A composition for promoting plant growth comprising the compound represented by the Formula (1) described in above [1] and inactive ingredients
[15] The method according to any one of [1] to [6], in which the plant is soybean.
[16] The method according to any one of [1] to [6], in which the plant is cotton.
›MODE FOR CARRYING OUT THE INVENTION · 1 of 73
Herein, the “promotion of the growth of a plant (hereinafter, sometimes described as “growth promotion”)” may mean the increase in the rate of seedling establishment, increase in the number of healthy leaves, increase in the height of the plant, increase in the weight of the plant, increase in the leaf area, increase in the number or weight of seeds or fruits, increase in the number of occasion of flower setting or fruit setting, and promoted growth of a root.
The growth promotion may be quantified by the following parameters.
(1) Rate of Seedling Establishment
Seeds of a plant are seeded in, for example, soil, filter paper, an agar medium, or sand and cultured for a certain period of time. Thereafter, the proportion of the surviving seedlings is examined.
(2) Number of Healthy Leaves or Proportion of Healthy Leaves
For each plant, the number of healthy leaves is counted, and the total number of healthy leaves is examined. Alternatively, a ratio of the number of healthy leaves to the total number of the leaves of the plant is examined.
(3) Plant Height
For each plant, a length from the base to the terminal branch or leave of the aerial part is measured.
(4) Plant Weight
The aerial part of each plant is cut and collected, and the weight thereof is measured to determine a fresh weight of the plant. Alternatively, the cut and collected sample is dried, and then a weight thereof is measured to determine a dry weight of the plant.
(5) Leaf Area
A plant is imaged with a digital camera, and the area of the green portion in the picture is quantified by image analysis software, for example, Win ROOF (manufactured by MITANI CORPORATION), or visually evaluated to determine a leaf area of the plant.
(6) Leaf Color
A leaf of a plant is sampled, and an amount of chlorophyll is measured using a chlorophyll meter (for example, SPAD-502, manufactured by Konica Minolta Sensing Europe B.V.) to determine the leaf color. In addition, the plant is imaged with a digital camera, and the area of the green portion in the picture is quantified by performing color extraction by using image analysis software, for example, Win ROOF (manufactured by MITANI CORPORATION), whereby the area of the green portion of the leaf of the plant is determined.
(7) Number or Weight of Seeds or Fruits
A plant is cultured until it produces seeds or fruits or until the seeds or fruits ripen, and then the number of fruits per plant or the total weight of fruits per plant is measured. Moreover, the plant is cultured until the seeds ripen, and then constituents of the yield, for example, the number of ears, ripening rate, and thousand kennel weight, are examined.
(8) Flower Setting Rate, Fruit Setting Rate, Fruition Rate, or Grain Filling Rare
A plant is cultured until it fruits, and the number of set flowers and fruits are counted to determine a fruit setting rate (number of set fruit/number of set flower×100). After the seeds ripen, the number of produced fruits and the number of filled grains are counted to determine a fruition rate (number of produced fruit/number of set flower×100) and a grain filling rate (number of filled grain/number of produced fruit×100) respectively.
(9) Promoted Growth of Root
A plant is cultured in soil or cultured hydroponically, and a length of the root is measured. Alternatively, the root is cut and collected, and a fresh weight thereof or the like is measured.
When a plant is treated with the compound of the present invention by the method of the present invention, the whole plant may be treated, or a portion thereof (foliage, a sprout, a flower, a fruit, an ear, a seed, a bulb, a tuber, a root, and the like) may be treated. Moreover, the plant may be treated at various growth stages thereof (a germination period including a pre-seeding stage, a seeding stage, a post-seeding stage, pre- and post-budding stages, and the like, a period of vegetative growth including a seedling stage, a seedling transplant stage, and a pre-cuttage stage or a seedling insertion stage, a growth stage after planting, a reproductive period including a pre-flowering stage, a flowering stage, a post-flowering stage, a stage immediately before emergence of ear, an ear emergence stage, and the like, a harvesting period including a stage prospect of harvest, a stage before prospect of ripening, the period during which fruits start to be colored, and the like). Herein, a bulb refers to a discoid stem, a corm, a rhizome, a tuberous root, a rhizophore, and the like. In addition, a seedling includes a nursery plant raised from a seed, a cuttage, and the like.
Examples of substituents to be used herein are described below with referring to specific examples.
Examples of the “halogen atom” in the compound of the present invention include a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, and the like.
Examples of the “C1-C6 alkyl group” in the compound of the present invention include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a 2,2-dimethylpropyl group, a 3-methylbutyl group, a 2,3-dimethylbutyl group, a 3,3-dimethylbutyl group, a hexyl group, and the like.
Examples of the “C1-C6 alkyl group optionally having one or more groups selected from the group X” in the compound of the present invention include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a 2,2-dimethylpropyl group, a 3-methylbutyl group, a 2,3-dimethylbutyl group, a 3,3-dimethylbutyl group, a hexyl group, a trichloromethyl group, a difluoromethyl group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a pentafluoroethyl group, a heptafluoropropyl group, a heptafluoroisopropyl group, a cyanomethyl group, a 2-cyanoethyl group, a methoxymethyl group, a 2-methoxyethyl group, an ethoxymethyl group, a 2-ethoxyethyl group, a trifluoromethoxymethyl group, a 2,2,2-trifluoroethoxymethyl group, and the like.
›MODE FOR CARRYING OUT THE INVENTION · 2 of 73
Examples of the “C1-C6 alkyl group optionally having one or more groups selected from the group Z” in the compound of the present invention include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a 2,2-dimethylpropyl group, a 3-methylbutyl group, a 2,3-dimethylbutyl group, 3,3-dimethylbutyl group, a hexyl group, a trichloromethyl group, a difluoromethyl group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a pentafluoroethyl group, a pentafluoropropyl group, a heptafluoroisopropyl group, a 2-hydroxyethyl group, a methoxymethyl group, a 2-methoxyethyl group, an ethoxymethyl group, a 2-ethoxyethyl group, a trifluoromethoxymethyl group, a 2,2,2-trifluoroethoxyethyl group, a methoxycarbonylmethyl group, and the like.
Examples of the “C1-C6 alkyl group optionally having one or more halogen atoms” in the compound of the present invention include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a 2,2-dimethylpropyl group, a 3-methylbutyl group, a 2,3-dimethylbutyl group, a 3,3-dimethylbutyl group, a hexyl group, a chloromethyl group, a trichloromethyl group, a difluoromethyl group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a pentafluoroethyl group, a heptafluoropropyl group, a heptafluoroisopropyl group, and the like.
Example of the “C1-C4 alkyl group” in the compound of the present invention include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group.
Examples of the “C1-C4 alkyl group optionally having one or more groups selected from the group X” in the compound of the present invention include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a chloromethyl group, a trichloromethyl group, a difluoromethyl group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a pentafluoroethyl group, a heptafluoropropyl group, a heptafluoroisopropyl group, a cyanomethyl group, a 2-cyanomethyl group, a methoxymethyl group, a 2-methoxyethyl group, an ethoxymethyl group, a 2-ethoxyethyl group, a trifluoromethoxymethyl group, a 2,2,2-trifluoroethoxymethyl group, and the like.
Examples of the “C1-C4 alkyl group optionally having one or more halogen atoms” in the compound of the present invention include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a trichloromethyl group, a difluoromethyl group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a pentafluoroethyl group, a heptafluoropropyl group, a heptafluoroisopropyl group, and the like.
Examples of the “C1-C3 alkyl group” in the compound of the present invention include a methyl group, an ethyl group, a propyl group, and an isopropyl group.
Examples of the “C1-C3 alkyl group optionally having one or more halogen atoms” in the compound of the present invention include a methyl group, an ethyl group, a propyl group, an isopropyl group, a difluoromethyl group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a pentafluoroethyl group, a heptafluoropropyl group, a heptafluoroisopropyl group, and the like.
Examples of the “C4-C7 cycloalkylalkyl group” in the compound of the present invention include a cyclopropyl methyl group, a 1-cyclopropyl ethyl group, a 2-cyclopropyl ethyl group, a cyclobutyl methyl group, a 1-cyclobutyl ethyl group, a cyclopentyl methyl group, a cyclohexyl methyl group, and the like.
Examples of the “C4-C7 cycloalkyl alkyl group optionally having one or more halogen atoms” in the compound of the present invention include a cyclopropylmethyl group, a 1-cyclopropylethyl group, a 2-cyclopropylethyl group, a cyclobutylmethyl group, a 1-cyclobutylethyl group, a cyclopentylmethyl group, a cyclohexylmethyl group, a 2,2-difluorocyclopropylmethyl group, a 1-(2,2-dichlorocyclopropyl)ethyl group, a 2,2-dibromocyclobutylmethyl group, a 2-chlorocyclopentylmethyl group, and the like.
Examples of the “C3-C6 cycloalkyl group” in the compound of the present invention include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, and the like.
Examples of the “C3-C6 cycloalkyl group optionally having one or more halogen atoms” in the compound of the present invention include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a 2,2-difluorocyclopropyl group, a 2,2-dichlorocyclopropyl group, a 2-chlorocyclopentyl group, a 4-iodocyclohexyl group, and the like.
Examples of the “C2-C6 alkenyl group” in the compound of the present invention include a vinyl group, a 1-propenyl group, an allyl group, an isopropenyl group, a 2-methyl-1-propenyl group, a 1-butenyl group, a 2-butenyl group, a 3-butenyl group, a 1-pentenyl group, a 1-hexenyl group, and the like.
Examples of the “C2-C6 alkenyl group optionally having one or more groups selected from the group X” in the compound of the present invention include a vinyl group, a 1-propenyl group, an allyl group, an isopropenyl group, a 2-methyl-1-propenyl group, a 1-butenyl group, a 2-butenyl group, a 3-butenyl group, a 1-pentenyl group, a 1-hexenyl group, a 2,2-difluoroethenyl group, a 2,2-dichloroethenyl group, a 2-cyano-1-ethenyl group, a 2-methoxy-1-ethenyl group, a 2-ethoxy-1-ethenyl group, a 3,3-difluoro-2-propenyl group, a 3,3-dichloro-2-propenyl group, a 4-methoxy-2-methyl-2-butenyl group, a 3-cyano-2-butenyl group, and the like.
Examples of the “C3-C6 alkenyl group” in the compound of the present invention include an allyl group, a 1-methyl-2-propenyl group, a 2-methyl-2-propenyl group, a 2-butenyl group, a 3-butenyl group, a 2-pentenyl group, a 4-pentenyl group, a 2-hexenyl group, a 5-hexenyl group, and the like.
Examples of the “C3-C6 alkenyl group optionally having one or more groups selected from the group X” in the compound of the present invention include an allyl group, a 1-methyl-2-propenyl group, a 2-methyl-2-propenyl group, a 2-butenyl group, a 3-butenyl group, a 2-pentenyl group, a 4-pentenyl group, a 2-hexenyl group, a 5-hexenyl group, a 3,3-difluoro-2-propenyl group, a 3,3-dichloro-2-propenyl group, a 4-methoxy-2-methyl-2-butenyl group, a 3-cyano-2-butenyl group, and the like.
›MODE FOR CARRYING OUT THE INVENTION · 3 of 73
Examples of the “C3-C6 alkenyl group optionally having one or more halogen atoms” in the compound of the present invention include a 2-propenyl group, a 1-methyl-2-propenyl group, a 2-methyl-2-propenyl group, a 2-butenyl group, a 3-butenyl group, a 2-pentenyl group, a 4-pentenyl group, a 2-hexenyl group, a 5-hexenyl group, a 3,3-difluoro-2-propenyl group, a 3,3-dichloro-2-propenyl group, and the like.
Examples of the “C2-C4 alkenyl group” in the compound of the present invention include a vinyl group, a 1-propenyl group, an allyl group, an isopropenyl group, a 2-methyl-1-propenyl group, a 1-butenyl group, a 2-butenyl group, a 3-butenyl group, and the like.
Examples of the “C2-C4 alkenyl group optionally having one or more halogen atoms” in the compound of the present invention include a vinyl group, a 1-propenyl group, an allyl group, an isopropenyl group, a 2-methyl-1-propenyl group, a 1-butenyl group, a 2-butenyl group, a 3-butenyl group, a 2,2-difluoroethenyl group, a 2,2-dichloroethenyl group, a 3,3-difluoro-2-propenyl group, a 3,3-dichloro-2-propenyl group, and the like.
Examples of the “C2-C6 alkynyl group” in the compound of the present invention include an ethynyl group, a 1-propynyl group, a propargyl group, a 1-butynyl group, a 2-butynyl group, a 3-butynyl group, a 3,3-dimethyl-1-butynyl group, a 1-pentynyl group, a 2-pentynyl group, a 1-hexynyl group, and the like.
Examples of the “C2-C6 alkynyl group optionally having one or more groups selected from the group X” in the compound of the present invention include an ethynyl group, a propargyl group, a 1-propynyl group, a 1-butynyl group, a 2-butynyl group, a 3-butynyl group, a 3,3-dimethyl-1-butynyl group, a 1-pentynyl group, a 1-hexynyl group, a 4-chloro-2-butynyl group, a 4-cyano-2-butynyl group, a 5-cyano-2-pentynyl group, a 4-methoxy-2-butynyl group, a 4-(2-chloroethoxy)-2-butynyl group, and the like.
Examples of the “C3-C6 alkynyl group” in the compound of the present invention include a propargyl group, a 2-butynyl group, a 3-butynyl group, a 2-pentynyl group, a 4-pentynyl group, a 2-hexynyl group, a 5-hexynyl group, and the like.
Examples of the “C3-C6 alkynyl group optionally having one or more groups selected from the group X” in the compound of the present invention include a propargyl group, a 2-butynyl group, a 3-butynyl group, a 2-pentynyl group, a 2-hexynyl group, a 4-chloro-2-butynyl group, a 4-cyano-2-butynyl group, a 5-cyano-2-pentynyl group, a 4-methoxy-2-butynyl group, a 4-(2-chloroethoxy)-2-butynyl group, and the like.
Examples of the “C3-C6 alkynyl group optionally having one or more halogen atoms” in the compound of the present invention include a propargyl group, a 2-butynyl group, a 3-butynyl group, a 3,3-dimethyl-1-butynyl group, a 2-pentynyl group, a 4-pentynyl group, a 2-hexynyl group, a 5-hexynyl group, a 4-chloro-2-butynyl group, and the like.
Examples of the “C2-C4 alkynyl group” in the compound of the present invention include an ethynyl group, a propargyl group, a 1-propynyl group, a 1-butynyl group, a 2-butynyl group, a 3-butynyl group, and the like.
Examples of the “C2-C4 alkynyl group optionally having one or more halogen atoms” in the compound of the present invention include an ethynyl group, a propargyl group, a 1-propynyl group, a 1-butynyl group, a 2-butynyl group, a 3-butynyl group, a 4-chloro-2-butynyl group, and the like.
Examples of the “C3-C4 alkynyl group” in the compound of the present invention include a propargyl group, a 2-butynyl group, a 3-butynyl group, and the like.
Examples of the “C3-C4 alkynyl group optionally having one or more groups selected from the group X” in the compound of the present invention include a propargyl group, a 2-butynyl group, a 3-butynyl group, a 4-chloro-2-butynyl group, a 4-methoxy-2-butynyl group, and the like.
Examples of the “phenyl group optionally having one or more groups selected from the group Y” in the compound of the present invention include a phenyl group, a 2-fluorophenyl group, a 3-fluorophenyl group, a 4-fluorophenyl group, a 2-chlorophenyl group, a 3-chlorophenyl group, a 4-chlorophenyl group, a 2-bromophenyl group, a 3-bromophenyl group, a 4-bromophenyl group, a 2-iodophenyl group, a 3-iodophenyl group, a 4-iodophenyl group, a 2-cyanophenyl group, a 3-cyanophenyl group, a 4-cyanophenyl group, a 2-nitrophenyl group, a 3-nitrophenyl group, a 4-nitrophenyl group, a 2-methylphenyl group, a 3-methylphenyl group, a 4-methylphenyl group, a 2-isopropylphenyl group, a 3-isopropylphenyl group, a 4-isopropylphenyl group, a 2-butylphenyl group, a 3-butylphenyl group, a 4-butylphenyl group, a 2-isobutylphenyl group, a 3-isobutylphenyl group, a 4-isobutylphenyl group, a 3-tert-butylphenyl group, a 4-tert-butylphenyl group, a 2-difluoromethylphenyl group, a 3-difluoromethylphenyl group, a 4-difluoromethylphenyl group, a 2-trifluoromethylphenyl group, a 3-trifluoromethylphenyl group, a 4-trifluoromethylphenyl group, a 2-(2,2,2-trifluoroethyl)phenyl group, a 3-(2,2,2-trifluoroethyl)phenyl group, a 4-(2,2,2-trifluoroethyl)phenyl group, a 2-pentafluoroethylphenol group, a 3-pentafluoroethylphenol group, a 4-pentafluoroethylphenyl group, a 2-heptafluoropropylphenyl group, a 3-heptafluoropropylphenyl group, a 4-heptafluoropropylphenyl group, a 2-heptafluoroisopropylphenyl group, a 3-heptafluoroisopropylphenyl group, a 4-heptafluoroisopropylphenyl group, a 2-methoxyphenyl group, a 3-methoxyphenyl group, a 4-methoxyphenyl group, a 2-tert-butoxyphenyl group, a 3-tert-butoxyphenyl group, a 4-tert-butoxyphenyl group, a 2-pentyloxyphenyl group, a 3-pentyloxyphenyl group, a 4-pentyloxyphenyl group, a 2-(2,2-dimethoxypropoxy)phenyl group, a 3-(2,2-dimethoxypropoxy)phenyl group, a 4-(2,2-dimethoxypropoxy)phenyl group, a 2-(3-methylbutoxy)phenyl group, a 3-(3-methylbutoxy)phenyl group, a 4-(3-methylbutoxy)phenyl group, a 2-difluoromethoxyphenyl group, a 3-difluoromethoxyphenyl group, a 4-difluoromethoxyphenyl group, a 2-trifluoromethoxyphenyl group, a 3-trifluoromethoxyphenyl group, a 4-trifluoromethoxyphenyl group, a 4-(2,2,2-trifluoroethoxy)phenyl group, a 2,4-dimethoxyphenyl group, a 3-chloro-4-methylphenyl group, and the like.
›MODE FOR CARRYING OUT THE INVENTION · 4 of 73
Examples of the “C7-C9 phenylalkyl group” in the compound of the present invention include a benzyl group, a 1-phenylethyl group, a 2-phenylethyl group, a 1-phenylpropyl group, a 2-phenylpropyl group, a 3-phenylpropyl group, a 1-methyl-1-phenylethyl group, and the like.
Examples of the “C7-C9 phenylalkyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y” in the compound of the present invention include a benzyl group, a 2-fluorobenzyl group, a 3-chlorobenzyl group, a 3-methoxybenzyl group, a 4-chlorobenzyl group, a 4-methylbenzyl group, a 4-trifluoromethyl group, a 1-(3-chlorophenyl)ethyl group, a 2-(4-bromophenyl)ethyl group, a 1-(2-cyanophenyl)propyl group, a 2-(3-nitrophenyl)propyl group, a 3-(3-methoxyphenyl)propyl group, a 1-methyl-1-(4-trifluoromethoxyphenyl)ethyl group, and the like.
Examples of the “benzyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y” in the compound of the present invention include a 2-fluorobenzyl group, a 3-chlorobenzyl group, a 4-bromobenzyl group, a 2-cyanobenzyl group, a 3-nitrobenzyl group, a 3-methoxybenzyl group, a 4-trifluoromethoxybenzyl group, a 4-chlorobenzyl group, a 4-methylbenzyl group, a 4-trifluoromethylbenzyl group, and the like.
Examples of the “6-membered aromatic heterocyclic group” in the compound of the present invention include a 2-pyridyl group, a 3-pyridyl group, a 4-pyridyl group, a 3-pyridazinyl group, a 4-pyridazinyl group, a 2-pyrimidinyl group, a 4-pyrimidinyl group, a 5-pyrimidinyl group, a 2-pyrazinyl group, a 4-(1,2,3-triazinyl) group, a 5-(1,2,3-triazinyl) group, a 3-(1,2,4-triazinyl) group, a 5-(1,2,4-triazinyl) group, a 6-(1,2,4-triazinyl) group, and a 2-(1,3,5-triazinyl) group, and the like.
Examples of the “6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y” in the compound of the present invention include a 2-pyridyl group, a 3-fluoro-2-pyridyl group, a 4-fluoro-2-pyridyl group, a 5-fluoro-2-pyridyl group, a 6-fluoro-2-pyridyl group, a 3-chloro-2-pyridyl group, a 4-chloro-2-pyridyl group, a 5-chloro-2-pyridyl group, a 6-chloro-2-pyridyl group, a 3-bromo-2-pyridyl group, a 4-bromo-2-pyridyl group, a 5-bromo-2-pyridyl group, a 6-bromo-2-pyridyl group, a 3-iodo-2-pyridyl group, a 4-iodo-2-pyridyl group, a 5-iodo-2-pyridyl group, a 6-iodo-2-pyridyl group, a 3-cyano-2-pyridyl group, a 4-cyano-2-pyridyl group, a 5-cyano-2-pyridyl group, a 6-cyano-2-pyridyl group, a 3-nitro-2-pyridyl group, a 4-nitro-2-pyridyl group, a 5-nitro-2-pyridyl group, a 6-nitro-2-pyridyl group, a 3-methyl-2-pyridyl group, a 4-methyl-2-pyridyl group, a 5-methyl-2-pyridyl group, a 6-methyl-2-pyridyl group, a 3-ethyl-2-pyridyl group, a 4-ethyl-2-pyridyl group, a 5-ethyl-2-pyridyl group, a 6-ethyl-2-pyridyl group, a 3-propyl-2-pyridyl group, a 4-propyl-2-pyridyl group, a 5-propyl-2-pyridyl group, a 6-propyl-2-pyridyl group, a 3-isopropyl-2-pyridyl group, a 4-isopropyl-2-pyridyl group, a 5-isopropyl-2-pyridyl group, a 6-isopropyl-2-pyridyl group, a 3-butyl-2-pyridyl group, a 4-butyl-2-pyridyl group, a 5-butyl-2-pyridyl group, a 6-butyl-2-pyridyl group, a 3-isobutyl-2-pyridyl group, a 4-isobutyl-2-pyridyl group, a 5-isobutyl-2-pyridyl group, a 6-isobutyl-2-pyridyl group, a 3-sec-butyl-2-pyridyl group, a 4-sec-butyl-2-pyridyl group, a 5-sec-butyl-2-pyridyl group, a 6-sec-butyl-2-pyridyl group, a 3-tert-butyl-2-pyridyl group, a 4-tert-butyl-2-pyridyl group, a 5-tert-butyl-2-pyridyl group, a 6-tert-butyl-2-pyridyl group, a 3-difluoromethyl-2-pyridyl group, a 4-difluoromethyl-2-pyridyl group, a 5-difluoromethyl-2-pyridyl group, a 6-difluoromethyl-2-pyridyl group, a 3-trifluoromethyl-2-pyridyl group, a 4-trifluoromethyl-2-pyridyl group, a 5-trifluoromethyl-2-pyridyl group, a 6-trifluoromethyl-2-pyridyl group, a 3-(2,2,2-trifluoroethyl)-2-pyridyl group, a 4-(2,2,2-trifluoroethyl)-2-pyridyl group, a 5-(2,2,2-trifluoroethyl)-2-pyridyl group, a 6-(2,2,2-trifluoroethyl)-2-pyridyl group, a 3-pentafluoroethyl-2-pyridyl group, a 4-pentafluoroethyl-2-pyridyl group, a 5-pentafluoroethyl-2-pyridyl group, a 6-pentafluoroethyl-2-pyridyl group, a 3-heptafluoropropyl-2-pyridyl group, a 4-heptafluoropropyl-2-pyridyl group, a 5-heptafluoropropyl-2-pyridyl group, a 6-heptafluoropropyl-2-pyridyl group, a 3-heptafluoroisopropyl-2-pyridyl group, a 4-heptafluoroisopropyl-2-pyridyl group, a 5-heptafluoroisopropyl-2-pyridyl group, a 6-heptafluoroisopropyl-2-pyridyl group, a 3-pyridyl group, a 2-methyl-3-pyridyl group, a 4-methyl-3-pyridyl group, a 5-methyl-3-pyridyl group, a 6-methyl-3-pyridyl group, a 2-ethyl-3-pyridyl group, a 4-ethyl-3-pyridyl group, a 5-ethyl-3-pyridyl group, a 6-ethyl-3-pyridyl group, a 2-propyl-3-pyridyl group, a 4-propyl-3-pyridyl group, a 5-propyl-3-pyridyl group, a 6-propyl-3-pyridyl group, a 2-isopropyl-3-pyridyl group, a 4-isopropyl-3-pyridyl group, a 5-isopropyl-3-pyridyl group, a 6-isopropyl-3-pyridyl group, a 2-butyl-3-pyridyl group, a 4-butyl-3-pyridyl group, a 5-butyl-3-pyridyl group, a 6-butyl-3-pyridyl group, a 2-isobutyl-3-pyridyl group, a 4-isobutyl-3-pyridyl group, a 5-isobutyl-3-pyridyl group, a 6-isobutyl-3-pyridyl group, a 2-sec-butyl-3-pyridyl group, a 4-sec-butyl-3-pyridyl group, a 5-sec-butyl-3-pyridyl group, a 6-sec-butyl-3-pyridyl group, a 2-tert-butyl-3-pyridyl group, a 4-tert-butyl-3-pyridyl group, a 5-tert-butyl-3-pyridyl group, a 6-tert-butyl-3-pyridyl group, a 2-difluoromethyl-3-pyridyl group, a 4-difluoromethyl-3-pyridyl group, a 5-difluoromethyl-3-pyridyl group, a 6-difluoromethyl-3-pyridyl group, a 2-trifluoromethyl-3-pyridyl group, a 4-trifluoromethyl-3-pyridyl group, a 5-trifluoromethyl-3-pyridyl group, a 6-trifluoromethyl-3-pyridyl group, a 2-(2,2,2-trifluoroethyl)-3-pyridyl group, a 4-(2,2,2-trifluoroethyl)-3-pyridyl group, a 5-(2,2,2-trifluoroethyl)-3-pyridyl group, a 6-(2,2,2-trifluoroethyl)-3-pyridyl group, a 2-pentafluoroethyl-3-pyridyl group, a 4-pentafluoroethyl-3-pyridyl group, a 5-pentafluoroethyl-3-pyridyl group, a 6-pentafluoroethyl-3-pyridyl group, a 2-heptafluoropropyl-3-pyridyl group, a 4-heptafluoropropyl-3-pyridyl group, a 5-heptafluoropropyl-3-pyridyl group, a 6-heptafluoropropyl-3-pyridyl group, a 2-heptafluoroisopropyl-3-pyridyl group, a 4-heptafluoroisopropyl-3-pyridyl group, a 5-heptafluoroisopropyl-3-pyridyl group, a 6-heptafluoroisopropyl-3-pyridyl group, a 4-pyridyl group, a 2-methyl-4-pyridyl group, a 3-methyl-4-pyridyl group, a 2-ethyl-4-pyridyl group, a 3-ethyl-4-pyridyl group, a 2-propyl-4-pyridyl group, a 3-propyl-4-pyridyl group, a 2-isopropyl-4-pyridyl group, a 3-isopropyl-4-pyridyl group, a 2-butyl-4-pyridyl group, a 3-butyl-4-pyridyl group, a 2-isobutyl-4-pyridyl group, a 3-isobutyl-4-pyridyl group, a 2-sec-butyl-4-pyridyl group, a 3-sec-butyl-4-pyridyl group, a 2-tert-butyl-4-pyridyl group, a 3-tert-butyl-4-pyridyl group, a 2-difluoromethyl-4-pyridyl group, a 3-difluoromethyl-4-pyridyl group, a 2-trifluoromethyl-4-pyridyl group, a 3-trifluoromethyl-4-pyridyl group, a 2-(2,2,2-trifluoroethyl)-4-pyridyl group, a 3-(2,2,2-trifluoroethyl)-4-pyridyl group, a 2-pentafluoroethyl-4-pyridyl group, a 3-pentafluoroethyl-4-pyridyl group, a 2-heptafluoropropyl-4-pyridyl group, a 3-heptafluoropropyl-4-pyridyl group, a 2-heptafluoroisopropyl-4-pyridyl group, a 3-heptafluoroisopropyl-4-pyridyl group, a 3-pyridazinyl group, a 4-methyl-3-pyridazinyl group, a 5-methyl-3-pyridazinyl group, a 6-methyl-3-pyridazinyl group, a 4-ethyl-3-pyridazinyl group, a 5-ethyl-3-pyridazinyl group, a 6-ethyl-3-pyridazinyl group, a 4-propyl-3-pyridazinyl group, a 5-propyl-3-pyridazinyl group, a 6-propyl-3-pyridazinyl group, a 4-isopropyl-3-pyridazinyl group, a 5-isopropyl-3-pyridazinyl group, a 6-isopropyl-3-pyridazinyl group, a 4-butyl-3-pyridazinyl group, a 5-butyl-3-pyridazinyl group, a 6-butyl-3-pyridazinyl group, a 4-isobutyl-3-pyridazinyl group, a 5-isobutyl-3-pyridazinyl group, a 6-isobutyl-3-pyridazinyl group, a 4-sec-butyl-3-pyridazinyl group, a 5-sec-butyl-3-pyridazinyl group, a 6-sec-butyl-3-pyridazinyl group, a 4-tert-butyl-3-pyridazinyl group, a 5-tert-butyl-3-pyridazinyl group, a 6-tert-butyl-3-pyridazinyl group, a 4-difluoromethyl-3-pyridazinyl group, a 5-difluoromethyl-3-pyridazinyl group, a 6-difluoromethyl-3-pyridazinyl group, a 4-trifluoromethyl-3-pyridazinyl group, a 5-trifluoromethyl-3-pyridazinyl group, a 6-trifluoromethyl-3-pyridazinyl group, a 4-(2,2,2-trifluoroethyl)-3-pyridazinyl group, a 5-(2,2,2-trifluoroethyl)-3-pyridazinyl group, a 6-(2,2,2-trifluoroethyl)-3-pyridazinyl group, a 4-pentafluoroethyl-3-pyridazinyl group, a 5-pentafluoroethyl-3-pyridazinyl group, a 6-pentafluoroethyl-3-pyridazinyl group, a 4-heptafluoropropyl-3-pyridazinyl group, a 5-heptafluoropropyl-3-pyridazinyl group, a 6-heptafluoropropyl-3-pyridazinyl group, a 4-heptafluoroisopropyl-3-pyridazinyl group, a 5-heptafluoroisopropyl-3-pyridazinyl group, a 6-heptafluoroisopropyl-3-pyridazinyl group, a 6-chloro-3-pyridazinyl group, a 6-methoxy-3-pyridazinyl group, a 6-cyano-3-pyridazinyl group, a 4-pyridazinyl group, a 3-methyl-4-pyridazinyl group, a 5-methyl-4-pyridazinyl group, a 6-methyl-4-pyridazinyl group, a 3-ethyl-4-pyridazinyl group, a 5-ethyl-4-pyridazinyl group, a 6-ethyl-4-pyridazinyl group, a 3-propyl-4-pyridazinyl group, a 5-propyl-4-pyridazinyl group, a 6-propyl-4-pyridazinyl group, a 3-isopropyl-4-pyridazinyl group, a 5-isopropyl-4-pyridazinyl group, a 6-isopropyl-4-pyridazinyl group, a 3-butyl-4-pyridazinyl group, a 5-butyl-4-pyridazinyl group, a 6-butyl-4-pyridazinyl group, a 3-isobutyl-4-pyridazinyl group, a 5-isobutyl-4-pyridazinyl group, a 6-isobutyl-4-pyridazinyl group, a 3-sec-butyl-4-pyridazinyl group, a 5-sec-butyl-4-pyridazinyl group, a 6-sec-butyl-4-pyridazinyl group, a 3-tert-butyl-4-pyridazinyl group, a 5-tert-butyl-4-pyridazinyl group, a 6-tert-butyl-4-pyridazinyl group, a 3-difluoromethyl-4-pyridazinyl group, a 5-difluoromethyl-4-pyridazinyl group, a 6-difluoromethyl-4-pyridazinyl group, a 3-trifluoromethyl-4-pyridazinyl group, a 5-trifluoromethyl-4-pyridazinyl group, a 6-trifluoromethyl-4-pyridazinyl group, a 3-(2,2,2-trifluoroethyl)-4-pyridazinyl group, a 5-(2,2,2-trifluoroethyl)-4-pyridazinyl group, a 6-(2,2,2-trifluoroethyl)-4-pyridazinyl group, a 3-pentafluoroethyl-4-pyridazinyl group, a 5-pentafluoroethyl-4-pyridazinyl group, a 6-pentafluoroethyl-4-pyridazinyl group, a 3-heptafluoropropyl-4-pyridazinyl group, a 5-heptafluoropropyl-4-pyridazinyl group, a 6-heptafluoropropyl-4-pyridazinyl group, a 3-heptafluoroisopropyl-4-pyridazinyl group, a 5-heptafluoroisopropyl-4-pyridazinyl group, a 6-heptafluoroisopropyl-4-pyridazinyl group, a 2-pyrimidinyl group, a 4-methyl-2-pyrimidinyl group, a 5-methyl-2-pyrimidinyl group, a 4-ethyl-2-pyrimidinyl group, a 5-ethyl-2-pyrimidinyl group, a 4-propyl-2-pyrimidinyl group, a 5-propyl-2-pyrimidinyl group, a 4-isopropyl-2-pyrimidinyl group, a 5-isopropyl-2-pyrimidinyl group, a 4-butyl-2-pyrimidinyl group, a 5-butyl-2-pyrimidinyl group, a 4-isobutyl-2-pyrimidinyl group, a 5-isobutyl-2-pyrimidinyl group, a 4-sec-butyl-2-pyrimidinyl group, a 5-sec-butyl-2-pyrimidinyl group, a 4-tert-butyl-2-pyrimidinyl group, a 5-tert-butyl-2-pyrimidinyl group, a 4-difluoromethyl-2-pyrimidinyl group, a 5-difluoromethyl-2-pyrimidinyl group, a 4-trifluoromethyl-2-pyrimidinyl group, a 5-trifluoromethyl-2-pyrimidinyl group, a 4-(2,2,2-trifluoroethyl)-2-pyrimidinyl group, a 5-(2,2,2-trifluoroethyl)-2-pyrimidinyl group, a 4-pentafluoroethyl-2-pyrimidinyl group, a 5-pentafluoroethyl-2-pyrimidinyl group, a 4-heptafluoropropyl-2-pyrimidinyl group, a 5-heptafluoropropyl-2-pyrimidinyl group, a 4-heptafluoroisopropyl-2-pyrimidinyl group, a 5-heptafluoroisopropyl-2-pyrimidinyl group, a 4-chloro-2-pyrimidinyl group, a 5-chloro-2-pyrimidinyl group, a 4-cyano-2-pyrimidinyl group, a 5-cyano-2-pyrimidinyl group, a 5-nitro-2-pyrimidinyl group, a 4-pyrimidinyl group, a 2-methyl-4-pyrimidinyl group, a 5-methyl-4-pyrimidinyl group, a 6-methyl-4-pyrimidinyl group, a 2-ethyl-4-pyrimidinyl group, a 5-ethyl-4-pyrimidinyl group, a 6-ethyl-4-pyrimidinyl group, a 2-propyl-4-pyrimidinyl group, a 5-propyl-4-pyrimidinyl group, a 6-propyl-4-pyrimidinyl group, a 2-isopropyl-4-pyrimidinyl group, a 5-isopropyl-4-pyrimidinyl group, a 6-isopropyl-4-pyrimidinyl group, a 2-butyl-4-pyrimidinyl group, a 5-butyl-4-pyrimidinyl group, a 6-butyl-4-pyrimidinyl group, a 2-isobutyl-4-pyrimidinyl group, a 5-isobutyl-4-pyrimidinyl group, a 6-isobutyl-4-pyrimidinyl group, a 2-sec-butyl-4-pyrimidinyl group, a 5-sec-butyl-4-pyrimidinyl group, a 6-sec-butyl-4-pyrimidinyl group, a 2-tert-butyl-4-pyrimidinyl group, a 5-tert-butyl-4-pyrimidinyl group, a 6-tert-butyl-4-pyrimidinyl group, a 2-difluoromethyl-4-pyrimidinyl group, a 5-difluoromethyl-4-pyrimidinyl group, a 6-difluoromethyl-4-pyrimidinyl group, a 2-trifluoromethyl-4-pyrimidinyl group, a 5-trifluoromethyl-4-pyrimidinyl group, a 6-trifluoromethyl-4-pyrimidinyl group, a 2-(2,2,2-trifluoroethyl)-4-pyrimidinyl group, a 5-(2,2,2-trifluoroethyl)-4-pyrimidinyl group, a 6-(2,2,2-trifluoroethyl)-4-pyrimidinyl group, a 2-heptafluoroethyl-4-pyrimidinyl group, a 5-heptafluoroethyl-4-pyrimidinyl group, a 6-heptafluoroethyl-4-pyrimidinyl group, a 2-heptafluoropropyl-4-pyrimidinyl group, a 5-heptafluoropropyl-4-pyrimidinyl group, a 6-heptafluoropropyl-4-pyrimidinyl group, a 2-heptafluoroisopropyl-4-pyrimidinyl group, a 5-heptafluoroisopropyl-4-pyrimidinyl group, a 6-heptafluoroisopropyl-4-pyrimidinyl group, a 2-chloro-4-pyrimidinyl group, a 2-cyano-4-pyrimidinyl group, a 5-chloro-4-pyrimidinyl group, a 5-cyano-4-pyrimidinyl group, a 5-nitro-4-pyrimidinyl group, a 5-pyrimidinyl group, a 2-methyl-5-pyrimidinyl group, a 4-methyl-5-pyrimidinyl group, a 2-ethyl-5-pyrimidinyl group, a 4-ethyl-5-pyrimidinyl group, a 2-propyl-5-pyrimidinyl group, a 4-propyl-5-pyrimidinyl group, a 2-isopropyl-5-pyrimidinyl group, a 4-isopropyl-5-pyrimidinyl group, a 2-butyl-5-pyrimidinyl group, a 4-butyl-5-pyrimidinyl group, a 2-isobutyl-5-pyrimidinyl group, a 4-isobutyl-5-pyrimidinyl group, a 2-sec-butyl-5-pyrimidinyl group, a 4-sec-butyl-5-pyrimidinyl group, a 2-tert-butyl-5-pyrimidinyl group, a 4-tert-butyl-5-pyrimidinyl group, a 2-difluoromethyl-5-pyrimidinyl group, a 4-difluoromethyl-5-pyrimidinyl group, a 2-trifluromethyl-5-pyrimidinyl group, a 4-trifluromethyl-5-pyrimidinyl group, a 2-(2,2,2-trifluoroethyl)-5-pyrimidinyl group, a 4-(2,2,2-trifluoroethyl)-5-pyrimidinyl group, a 2-pentafluoroethyl-5-pyrimidinyl group, a 4-pentafluoroethyl-5-pyrimidinyl group, a 2-heptafluoropropyl-5-pyrimidinyl group, a 4-heptafluoropropyl-5-pyrimidinyl group, a 2-heptafluoroisopropyl-5-pyrimidinyl group, a 4-heptafluoroisopropyl-5-pyrimidinyl group, a 2-pyrazinyl group, a 3-methyl-2-pyrazinyl group, a 5-methyl-2-pyrazinyl group, a 6-methyl-2-pyrazinyl group, a 3-ethyl-2-pyrazinyl group, a 5-ethyl-2-pyrazinyl group, a 6-ethyl-2-pyrazinyl group, a 3-propyl-2-pyrazinyl group, a 5-propyl-2-pyrazinyl group, a 6-propyl-2-pyrazinyl group, a 3-isopropyl-2-pyrazinyl group, a 5-isopropyl-2-pyrazinyl group, a 6-isopropyl-2-pyrazinyl group, a 3-butyl-2-pyrazinyl group, a 5-butyl-2-pyrazinyl group, a 6-butyl-2-pyrazinyl group, a 3-isobutyl-2-pyrazinyl group, a 5-isobutyl-2-pyrazinyl group, a 6-isobutyl-2-pyrazinyl group, a 3-sec-butyl-2-pyrazinyl group, a 5-sec-butyl-2-pyrazinyl group, a 6-sec-butyl-2-pyrazinyl group, a 3-tert-butyl-2-pyrazinyl group, a 5-tert-butyl-2-pyrazinyl group, a 6-tert-butyl-2-pyrazinyl group, a 3-difluoromethyl-2-pyrazinyl group, a 5-difluoromethyl-2-pyrazinyl group, a 6-difluoromethyl-2-pyrazinyl group, a 3-trifluoromethyl-2-pyrazinyl group, a 5-trifluoromethyl-2-pyrazinyl group, a 6-trifluoromethyl-2-pyrazinyl group, a 3-(2,2,2-trifluoroethyl)-2-pyrazinyl group, a 5-(2,2,2-trifluoroethyl)-2-pyrazinyl group, a 6-(2,2,2-trifluoroethyl)-2-pyrazinyl group, a 3-pentafluoroethyl-2-pyrazinyl group, a 5-pentafluoroethyl-2-pyrazinyl group, a 6-pentafluoroethyl-2-pyrazinyl group, a 3-heptafluoropropyl-2-pyrazinyl group, a 5-heptafluoropropyl-2-pyrazinyl group, a 6-heptafluoropropyl-2-pyrazinyl group, a 3-heptafluoroisopropyl-2-pyrazinyl group, a 5-heptafluoroisopropyl-2-pyrazinyl group, a 6-heptafluoroisopropyl-2-pyrazinyl group, a 3-chloro-2-pyrazinyl group, a 3-cyano-2-pyrazinyl group, a 3-nitro-2-pyrazinyl group, a 5-chloro-2-pyrazinyl group, a 5-cyano-2-pyrazinyl group, a 5-nitro-2-pyrazinyl group, a 6-chloro-2-pyrazinyl group, a 4-(1,2,3-triazinyl) group, a 5-methyl-4-(1,2,3-triazinyl) group, a 6-methyl-4-(1,2,3-triazinyl) group, a 5-ethyl-4-(1,2,3-triazinyl) group, a 6-ethyl-4-(1,2,3-triazinyl) group, a 5-propyl-4-(1,2,3-triazinyl) group, a 6-propyl-4-(1,2,3-triazinyl) group, a 5-isopropyl-4-(1,2,3-triazinyl) group, a 6-isopropyl-4-(1,2,3-triazinyl) group, a 5-butyl-4-(1,2,3-triazinyl) group, a 6-butyl-4-(1,2,3-triazinyl) group, a 5-isobutyl-4-(1,2,3-triazinyl) group, a 6-isobutyl-4-(1,2,3-triazinyl) group, a 5-sec-butyl-4-(1,2,3-triazinyl) group, a 6-sec-butyl-4-(1,2,3-triazinyl) group, a 5-tert-butyl-4-(1,2,3-triazinyl) group, a 6-tert-butyl-4-(1,2,3-triazinyl) group, a 5-difluoromethyl-4-C1,2,3-triazinyl) group, a 6-difluoromethyl-4-(1,2,3-triazinyl) group, a 5-trifluoromethyl-4-(1,2,3-triazinyl) group, a 6-trifluoromethyl-4-(1,2,3-triazinyl) group, a 5-(2,2,2-trifluoroethyl)-4-(1,2,3-triazinyl) group, a 6-(2,2,2-trifluoroethyl)-4-(1,2,3-triazinyl) group, a 5-pentafluoroethyl-4-(1,2,3-triazinyl) group, a 6-pentafluoroethyl-4-(1,2,3-triazinyl) group, a 5-heptafluoropropyl-4-(1,2,3-triazinyl) group, a 6-heptafluoropropyl-4-(1,2,3-triazinyl) group, a 5-heptafluoroisopropyl-4-(1,2,3-triazinyl) group, a 6-heptafluoroisopropyl-4-(1,2,3-triazinyl) group, a 5-(1,2,3-triazinyl) group, a 4-methyl-5-(1,2,3-triazinyl)group, a 4-ethyl-5-(1,2,3-triazinyl)group, a 4-propyl-5-(1,2,3-triazinyl)group, a 4-isopropyl-5-(1,2,3-triazinyl) group, a 4-butyl-5-(1,2,3-triazinyl)group, a 4-isobutyl-5-(1,2,3-triazinyl) group, a 4-sec-butyl-5-(1,2,3-triazinyl)group, a 4-tert-butyl-5-(1,2,3-triazinyl)group, a 4-difluoromethyl-5-(1,2,3-triazinyl)group, a 4-trifluoromethyl-5-(1,2,3-triazinyl)group, a 4-(2,2,2-trifluoroethyl)-5-(1,2,3-triazinyl)group, a 4-pentafluoroethyl-5-(1,2,3-triazinyl) group, a 4-heptafluoropropyl-5-(1,2,3-triazinyl)group, a 4-heptafluoroisopropyl-5-(1,2,3-triazinyl) group, a 3-(1,2,4-triazinyl) group, a 5-methyl-3-(1,2,4-triazinyl)group, a 6-methyl-3-(1,2,4-triazinyl)group, a 5-ethyl-3-(1,2,4-triazinyl)group, a 6-ethyl-3-(1,2,4-triazinyl) group, a 5-propyl-3-(1,2,4-triazinyl) group, a 6-propyl-3-(1,2,4-triazinyl)group, a 5-isopropyl-3-(1,2,4-triazinyl)group, a 6-isopropyl-3-(1,2,4-triazinyl)group, a 5-butyl-3-(1,2,4-triazinyl)group, a 6-butyl-3-(1,2,4-triazinyl)group, a 5-isobutyl-3-(1,2,4-triazinyl)group, a 6-isobutyl-3-(1,2,4-triazinyl)group, a 5-sec-butyl-3-(1,2,4-triazinyl)group, a 6-sec-butyl-3-(1,2,4-triazinyl)group, a 5-tert-butyl-3-(1,2,4-triazinyl)group, a 6-tert-butyl-3-(1,2,4-triazinyl)group, a 5-difluoromethyl-3-(1,2,4-triazinyl)group, a 6-difluoromethyl-3-(1,2,4-triazinyl)group, a 5-trifluoromethyl-3-(1,2,4-triazinyl)group, a 6-trifluoromethyl-3-(1,2,4-triazinyl)group, a 5-(2,2,2-trifluoroethyl)-3-(1,2,4-triazinyl)group, a 6-(2,2,2-trifluoroethyl)-3-(1,2,4-triazinyl)group, a 5-pentafluoroethyl-3-(1,2,4-triazinyl)group, a 6-pentafluoroethyl-3-(1,2,4-triazinyl)group, a 5-heptafluoropropyl-3-(1,2,4-triazinyl)group, a 6-heptafluoropropyl-3-(1,2,4-triazinyl)group, a 5-heptafluoroisopropyl-3-(1,2,4-triazinyl)group, a 6-heptafluoroisopropyl-3-(1,2,4-triazinyl)group, a 5-(1,2,4-triazinyl)group, a 3-methyl-5-(1,2,4-triazinyl)group, a 6-methyl-5-(1,2,4-triazinyl)group, a 3-ethyl-5-(1,2,4-triazinyl)group, a 6-ethyl-5-(1,2,4-triazinyl)group, a 3-propyl-5-(1,2,4-triazinyl)group, a 6-propyl-5-(1,2,4-triazinyl)group, a 3-isopropyl-5-(1,2,4-triazinyl)group, a 6-isopropyl-5-(1,2,4-triazinyl)group, a 3-butyl-5-(1,2,4-triazinyl)group, a 6-butyl-5-(1,2,4-triazinyl)group, a 3-isobutyl-5-(1,2,4-triazinyl)group, a 6-isobutyl-5-(1,2,4-triazinyl)group, a 3-sec-butyl-5-(1,2,4-triazinyl)group, a 6-sec-butyl-5-(1,2,4-triazinyl)group, a 3-tert-butyl-5-(1,2,4-triazinyl)group, a 6-tert-butyl-5-(1,2,4-triazinyl)group, a 3-difluoromethyl-5-(1,2,4-triazinyl)group, a 6-difluoromethyl-5-(1,2,4-triazinyl) group, a 3-trifluoromethyl-5-(1,2,4-triazinyl)group, a 6-trifluoromethyl-5-(1,2,4-triazinyl)group, a 3-(2,2,2-trifluoroethyl)-5-(1,2,4-triazinyl)group, a 6-(2,2,2-trifluoroethyl)-5-(1,2,4-triazinyl)group, a 3-pentafluoroethyl-5-(1,2,4-triazinyl)group, a 6-pentafluoroethyl-5-(1,2,4-triazinyl) group, a 3-heptafluoropropyl-5-(1,2,4-triazinyl) group, a 6-heptafluoropropyl-5-(1,2,4-triazinyl)group, a 3-heptafluoroisopropyl-5-(1,2,4-triazinyl)group, a 6-heptafluoroisopropyl-5-(1,2,4-triazinyl)group, a 6-(1,2,4-triazinyl)group, a 3-methyl-6-(1,2,4-triazinyl)group, a 5-methyl-6-(1,2,4-triazinyl)group, a 3-ethyl-6-(1,2,4-triazinyl)group, a 5-ethyl-6-(1,2,4-triazinyl)group, a 3-propyl-6-(1,2,4-triazinyl)group, a 5-propyl-6-(1,2,4-triazinyl)group, a 3-isopropyl-6-(1,2,4-triazinyl)group, a 5-isopropyl-6-(1,2,4-triazinyl)group, a 3-butyl-6-(1,2,4-triazinyl)group, a 5-butyl-6-(1,2,4-triazinyl)group, a 3-isobutyl-6-(1,2,4-triazinyl)group, a 5-isobutyl-6-(1,2,4-triazinyl)group, a 3-sec-butyl-6-(1,2,4-triazinyl)group, a 5-sec-butyl-6-(1,2,4-triazinyl)group, a 3-tert-butyl-6-(1,2,4-triazinyl)group, a 5-tert-butyl-6-(1,2,4-triazinyl)group, a 3-difluoromethyl-6-(1,2,4-triazinyl)group, a 5-difluoromethyl-6-(1,2,4-triazinyl)group, 3-trifluoromethyl-6-(1,2,4-triazinyl)group, 5-trifluoromethyl-6-(1,2,4-triazinyl)group, a 3-(2,2,2-trifluoroethyl)-6-(1,2,4-triazinyl)group, a 5-(2,2,2-trifluoroethyl)-6-(1,2,4-triazinyl)group, a 3-pentafluoroethyl-6-(1,2,4-triazinyl)group, a 5-pentafluoroethyl-6-(1,2,4-triazinyl)group, a 3-heptafluoropropyl-6-(1,2,4-triazinyl)group, a 5-heptafluoropropyl-6-(1,2,4-triazinyl)group, 3-heptafluoroisopropyl-6-(1,2,4-triazinyl)group, a 5-heptafluoroisopropyl-6-(1,2,4-triazinyl)group, a 2-(1,3,5-triazinyl)group, a 4-chloro-2-(1,3,5-triazinyl)group, a 4,6-dichloro-2-(1,3,5-triazinyl)group, a 4-methyl-2-(1,3,5-triazinyl)group, a 4-ethyl-2-(1,3,5-triazinyl)group, a 4-propyl-2-(1,3,5-triazinyl)group, a 4-isopropyl-2-(1,3,5-triazinyl)group, a 4-butyl-2-(1,3,5-triazinyl)group, a 4-isobutyl-2-(1,3,5-triazinyl)group, a 4-sec-butyl-2-(1,3,5-triazinyl)group, a 4-tert-butyl-2-(1,3,5-triazinyl)group, a 4-difluoromethyl-2-(1,3,5-triazinyl)group, a 4-trifluoromethyl-2-(1,3,5-triazinyl)group, a 4-(2,2,2-trifluoroethyl)-2-(1,3,5-triazinyl)group, 4-pentafluoroethyl-2-(1,3,5-triazinyl)group, 4-heptafluoropropyl-2-(1,3,5-triazinyl)group, 4-heptafluoroisopropyl-2-(1,3,5-triazinyl)group, and the like.
›MODE FOR CARRYING OUT THE INVENTION · 5 of 73
Examples of the “6-membered aromatic heterocyclic —C1-C3 alkyl group” in the compound of the present invention include a 2-pyridylmethyl group, a 2-(2-pyridyl)ethyl group, a 1-(2-pyridyl)propyl group, a 3-pyridylmethyl group, a 4-pyridylmethyl group, a 3-pyridazinylmethyl group, a 2-pyrimidinylmethyl group, a 2-pyrazinylmethyl group, a 1-[4-(1,2,3-triazinyl)]ethyl group, and the like.
Examples of the 6-membered aromatic heterocyclic C1-C3 alkyl group wherein a 6-membered aromatic heterocyclic portion may have optionally one or more groups selected from the group Y” in the compound of the present invention include a 2-pyridylmethyl group, a 3-fluoro-2-pyridylmethyl group, a 5-chloro-2-pyridylmethyl group, a 5-trifluoromethyl-2-pyridylmethyl group, a 2-(4-chloro-2-pyridyl)ethyl group, a 1-(5-bromo-2-pyridyl)propyl group, a 6-bromo-2-pyridylmethyl group, a 3-iodo-2-pyridylmethyl group, a 4-cyano-2-pyridylmethyl group, a 5-nitro-2-pyridylmethyl group, a 6-methyl-2-pyridylmethyl group, a 3-difluoromethyl-2-pyridylmethyl group, a 4-trifluoromethyl-2-pyridylmethyl group, a 3-pyridylmethyl group, a 6-chloro-3-pyridylmethyl group, a 4-pyridylmethyl group, a 2-chloro-4-pyridylmethyl group, a 4-methyl-3-pyridazinylmethyl group, a 6-difluoromethyl-3-pyridazinylmethyl group, a 4-trifluoromethyl-3-pyridazinylmethyl group, a 4-methyl-2-pyrimidinylmethyl group, a 5-difluoromethyl-2-pyrimidinylmethyl group, a 5-trifluoromethyl-2-pyrimidinylmethyl group, a 5-isopropyl-2-pyrazinylmethyl group, a 5-difluoromethyl-2-pyrazinylmethyl group, a 6-trifluoromethyl-2-pyrazinylmethyl group, a 3-(2,2,2-trifluoroethyl)-2-pyrazinylmethyl group, a 1-[5-tert-butyl-4-(1,2,3-triazinyl)]ethyl group, and the like.
Examples of the “pyridyl group optionally having one or more groups selected from the group Y” in the compound of the present invention include a 2-pyridyl group, a 3-fluoro-2-pyridyl group, a 4-fluoro-2-pyridyl group, a 5-fluoro-2-pyridyl group, a 6-fluoro-2-pyridyl group, a 3-chloro-2-pyridyl group, a 4-chloro-2-pyridyl group, a 5-chloro-2-pyridyl group, a 6-chloro-2-pyridyl group, a 3-bromo-2-pyridyl group, a 4-bromo-2-pyridyl group, a 5-bromo-2-pyridyl group, a 6-bromo-2-pyridyl group, a 3-iodo-2-pyridyl group, a 4-iodo-2-pyridyl group, a 5-iodo-2-pyridyl group, a 6-iodo-2-pyridyl group, a 3-cyano-2-pyridyl group, a 4-cyano-2-pyridyl group, a 5-cyano-2-pyridyl group, a 6-cyano-2-pyridyl group, a 3-nitro-2-pyridyl group, a 4-nitro-2-pyridyl group, a 5-nitro-2-pyridyl group, a 6-nitro-2-pyridyl group, a 3-methyl-2-pyridyl group, a 4-methyl-2-pyridyl group, a 5-methyl-2-pyridyl group, a 6-methyl-2-pyridyl group, a 3-ethyl-2-pyridyl group, a 4-ethyl-2-pyridyl group, a 5-ethyl-2-pyridyl group, a 6-ethyl-2-pyridyl group, a 3-propyl-2-pyridyl group, a 4-propyl-2-pyridyl group, a 5-propyl-2-pyridyl group, a 6-propyl-2-pyridyl group, a 3-isopropyl-2-pyridyl group, a 4-isopropyl-2-pyridyl group, a 5-isopropyl-2-pyridyl group, a 6-isopropyl-2-pyridyl group, a 3-butyl-2-pyridyl group, a 4-butyl-2-pyridyl group, a 5-butyl-2-pyridyl group, a 6-butyl-2-pyridyl group, a 3-isobutyl-2-pyridyl group, a 4-isobutyl-2-pyridyl group, a 5-isobutyl-2-pyridyl group, a 6-isobutyl-2-pyridyl group, a 3-sec-butyl-2-pyridyl group, a 4-sec-butyl-2-pyridyl group, a 5-sec-butyl-2-pyridyl group, a 6-sec-butyl-2-pyridyl group, a 3-tert-butyl-2-pyridyl group, a 4-tert-butyl-2-pyridyl group, a 5-tert-butyl-2-pyridyl group, a 6-tert-butyl-2-pyridyl group, a 3-difluoromethyl-2-pyridyl group, a 4-difluoromethyl-2-pyridyl group, a 5-difluoromethyl-2-pyridyl group, a 6-difluoromethyl-2-pyridyl group, a 3-trifluoromethyl-2-pyridyl group, a 4-trifluoromethyl-2-pyridyl group, a 5-trifluoromethyl-2-pyridyl group, a 6-trifluoromethyl-2-pyridyl group, a 3-(2,2,2-trifluoroethyl)-2-pyridyl group, a 4-(2,2,2-trifluoroethyl)-2-pyridyl group, a 5-(2,2,2-trifluoroethyl)-2-pyridyl group, a 6-(2,2,2-trifluoroethyl)-2-pyridyl group, a 3-pentafluoroethyl-2-pyridyl group, a 4-pentafluoroethyl-2-pyridyl group, a 5-pentafluoroethyl-2-pyridyl group, a 6-pentafluoroethyl-2-pyridyl group, a 3-heptafluoropropyl-2-pyridyl group, a 4-heptafluoropropyl-2-pyridyl group, a 5-heptafluoropropyl-2-pyridyl group, a 6-heptafluoropropyl-2-pyridyl group, a 3-heptafluoroisopropyl-2-pyridyl group, a 4-heptafluoroisopropyl-2-pyridyl group, a 5-heptafluoroisopropyl-2-pyridyl group, a 6-heptafluoroisopropyl-2-pyridyl group, a 3-pyridyl group, a 2-methyl-3-pyridyl group, a 4-methyl-3-pyridyl group, a 5-methyl-3-pyridyl group, a 6-methyl-3-pyridyl group, a 2-ethyl-3-pyridyl group, a 4-ethyl-3-pyridyl group, a 5-ethyl-3-pyridyl group, a 6-ethyl-3-pyridyl group, a 2-propyl-3-pyridyl group, a 4-propyl-3-pyridyl group, a 5-propyl-3-pyridyl group, a 6-propyl-3-pyridyl group, a 2-isopropyl-3-pyridyl group, a 4-isopropyl-3-pyridyl group, a 5-isopropyl-3-pyridyl group, a 6-isopropyl-3-pyridyl group, a 2-butyl-3-pyridyl group, a 4-butyl-3-pyridyl group, a 5-butyl-3-pyridyl group, a 6-butyl-3-pyridyl group, a 2-isobutyl-3-pyridyl group, a 4-isobutyl-3-pyridyl group, a 5-isobutyl-3-pyridyl group, a 6-isobutyl-3-pyridyl group, a 2-sec-butyl-3-pyridyl group, a 4-sec-butyl-3-pyridyl group, a 5-sec-butyl-3-pyridyl group, a 6-sec-butyl-3-pyridyl group, a 2-tert-butyl-3-pyridyl group, a 4-tert-butyl-3-pyridyl group, a 5-tert-butyl-3-pyridyl group, a 6-tert-butyl-3-pyridyl group, a 2-difluoromethyl-3-pyridyl group, a 4-difluoromethyl-3-pyridyl group, a 5-difluoromethyl-3-pyridyl group, a 6-difluoromethyl-3-pyridyl group, a 2-trifluoromethyl-3-pyridyl group, a 4-trifluoromethyl-3-pyridyl group, a 5-trifluoromethyl-3-pyridyl group, a 6-trifluoromethyl-3-pyridyl group, a 2-(2,2,2-trifluoroethyl)-3-pyridyl group, a 4-(2,2,2-trifluoroethyl)-3-pyridyl group, a 5-(2,2,2-trifluoroethyl)-3-pyridyl group, a 6-(2,2,2-trifluoroethyl)-3-pyridyl group, a 2-pentafluoroethyl-3-pyridyl group, a 4-pentafluoroethyl-3-pyridyl group, a 5-pentafluoroethyl-3-pyridyl group, a 6-pentafluoroethyl-3-pyridyl group, a 2-heptafluoropropyl-3-pyridyl group, a 4-heptafluoropropyl-3-pyridyl group, a 5-heptafluoropropyl-3-pyridyl group, a 6-heptafluoropropyl-3-pyridyl group, a 2-heptafluoroisopropyl-3-pyridyl group, a 4-heptafluoroisopropyl-3-pyridyl group, a 5-heptafluoroisopropyl-3-pyridyl group, a 6-heptafluoroisopropyl-3-pyridyl group, a 4-pyridyl group, a 2-methyl-4-pyridyl group, a 3-methyl-4-pyridyl group, a 2-ethyl-4-pyridyl group, a 3-ethyl-4-pyridyl group, a 2-propyl-4-pyridyl group, a 3-propyl-4-pyridyl group, a 2-isopropyl-4-pyridyl group, a 3-isopropyl-4-pyridyl group, a 2-butyl-4-pyridyl group, a 3-butyl-4-pyridyl group, a 2-isobutyl-4-pyridyl group, a 3-isobutyl-4-pyridyl group, a 2-sec-butyl-4-pyridyl group, a 3-sec-butyl-4-pyridyl group, a 2-tert-butyl-4-pyridyl group, a 3-tert-butyl-4-pyridyl group, a 2-difluoromethyl-4-pyridyl group, a 3-difluoromethyl-4-pyridyl group, a 2-trifluoromethyl-4-pyridyl group, a 3-trifluoromethyl-4-pyridyl group, a 2-(2,2,2-trifluoroethyl)-4-pyridyl group, a 3-(2,2,2-trifluoroethyl)-4-pyridyl group, a 2-heptafluoropropyl-4-pyridyl group, a 3-heptafluoropropyl-4-pyridyl group, a 2-heptafluoroisopropyl-4-pyridyl group, a 3-heptafluoroisopropyl-4-pyridyl group, and the like.
›MODE FOR CARRYING OUT THE INVENTION · 6 of 73
Examples of the “pyridyl C1-C3 alkyl group” in the compound of the present invention include a 2-pyridylmethyl group, a 3-pyridylmethyl group, a 4-pyridylmethyl group, a 2-(2-pyridyl)ethyl group, a 1-(2-pyridyl)propyl group, and the like.
Examples of the “pyridyl-C1-C3 alkyl group wherein a pyridine ring portion may have optionally one or more groups selected from the group Y” in the compound of the present invention include a 2-pyridylmethyl group, a 3-pyridylmethyl group, a 4-pyridylmethyl group, a (3-fluoro-2-pyridyl)methyl group, a (5-chloro-2-pyridyl)methyl group, a 2-(4-chloro-2-pyridyl)ethyl group, a 1-(5-bromo-2-pyridyl)propyl group, a (6-bromo-2-pyridyl)methyl group, a (3-iodo-2-pyridyl)methyl group, a (4-cyano-2-pyridyl)methyl group, a (5-nitro-2-pyridyl)methyl group, a (6-methyl-2-pyridyl)methyl group, a (3-difluoromethyl-2-pyridyl)methyl group, a (4-trifluoromethyl-2-pyridyl)methyl group, a (5-trifluoromethyl-2-pyridyl)methyl group, a (6-chloro-3-pyridyl)methyl group, a (2-chloro-4-pyridyl)methyl group, and the like.
Examples of the “pyrimidinyl group optionally having one or more groups selected from the group Y” in the compound of the present invention include a 2-pyrimidinyl group, a 4-methyl-2-pyrimidinyl group, a 5-methyl-2-pyrimidinyl group, a 4-ethyl-2-pyrimidinyl group, a 5-ethyl-2-pyrimidinyl group, a 4-propyl-2-pyrimidinyl group, a 5-propyl-2-pyrimidinyl group, a 4-isopropyl-2-pyrimidinyl group, a 5-isopropyl-2-pyrimidinyl group, a 4-butyl-2-pyrimidinyl group, a 5-butyl-2-pyrimidinyl group, a 4-isobutyl-2-pyrimidinyl group, a 5-isobutyl-2-pyrimidinyl group, a 4-sec-butyl-2-pyrimidinyl group, a 5-sec-butyl-2-pyrimidinyl group, a 4-tert-butyl-2-pyrimidinyl group, a 5-tert-butyl-2-pyrimidinyl group, a 4-difluoromethyl-2-pyrimidinyl group, a 5-difluoromethyl-2-pyrimidinyl group, a 4-trifluoromethyl-2-pyrimidinyl group, a 5-trifluoromethyl-2-pyrimidinyl group, a 4-(2,2,2-trifluoroethyl)-2-pyrimidinyl group, a 5-(2,2,2-trifluoroethyl)-2-pyrimidinyl group, a 4-pentafluoroethyl-2-pyrimidinyl group, a 5-pentafluoroethyl-2-pyrimidinyl group, a 4-heptafluoropropyl-2-pyrimidinyl group, a 5-heptafluoropropyl-2-pyrimidinyl group, a 4-heptafluoroisopropyl-2-pyrimidinyl group, a 5-heptafluoroisopropyl-2-pyrimidinyl group, a 4-pyrimidinyl group, a 2-methyl-4-pyrimidinyl group, a 5-methyl-4-pyrimidinyl group, a 6-methyl-4-pyrimidinyl group, a 2-ethyl-4-pyrimidinyl group, a 5-ethyl-4-pyrimidinyl group, a 6-ethyl-4-pyrimidinyl group, a 2-propyl-4-pyrimidinyl group, a 5-propyl-4-pyrimidinyl group, a 6-propyl-4-pyrimidinyl group, a 2-isopropyl-4-pyrimidinyl group, a 5-isopropyl-4-pyrimidinyl group, a 6-isopropyl-4-pyrimidinyl group, a 2-butyl-4-pyrimidinyl group, a 5-butyl-4-pyrimidinyl group, a 6-butyl-4-pyrimidinyl group, a 2-isobutyl-4-pyrimidinyl group, a 5-isobutyl-4-pyrimidinyl group, a 6-isobutyl-4-pyrimidinyl group, a 2-sec-butyl-4-pyrimidinyl group, a 5-sec-butyl-4-pyrimidinyl group, a 6-sec-butyl-4-pyrimidinyl group, a 2-tert-butyl-4-pyrimidinyl group, a 5-tert-butyl-4-pyrimidinyl group, a 6-tert-butyl-4-pyrimidinyl group, a 2-difluoromethyl-4-pyrimidinyl group, a 5-difluoromethyl-4-pyrimidinyl group, a 6-difluoromethyl-4-pyrimidinyl group, a 2-trifluoromethyl-4-pyrimidinyl group, a 5-trifluoromethyl-4-pyrimidinyl group, a 6-trifluoromethyl-4-pyrimidinyl group, a 2-(2,2,2-trifluoroethyl-4-pyrimidinyl group, a 5-(2,2,2-trifluoroethyl)-4-pyrimidinyl group, a 6-(2,2,2-trifluoroethyl)-4-pyrimidinyl group, a 2-pentafluoroethyl-4-pyrimidinyl group, a 5-pentafluoroethyl-4-pyrimidinyl group, a 6-pentafluoroethyl-4-pyrimidinyl group, a 2-heptafluoropropyl-4-pyrimidinyl group, a 5-heptafluoropropyl-4-pyrimidinyl group, a 6-heptafluoropropyl-4-pyrimidinyl group, a 2-heptafluoroisopropyl-4-pyrimidinyl group, a 5-heptafluoroisopropyl-4-pyrimidinyl group, a 6-heptafluoroisopropyl-4-pyrimidinyl group, a 5-pyrimidinyl group, a 2-methyl-5-pyrimidinyl group, a 4-methyl-5-pyrimidinyl group, a 2-ethyl-5-pyrimidinyl group, a 4-ethyl-5-pyrimidinyl group, a 2-propyl-5-pyrimidinyl group, a 4-propyl-5-pyrimidinyl group, a 2-isopropyl-5-pyrimidinyl group, a 4-isopropyl-5-pyrimidinyl group, a 2-butyl-5-pyrimidinyl group, a 4-butyl-5-pyrimidinyl group, a 2-isobutyl-5-pyrimidinyl group, a 4-isobutyl-5-pyrimidinyl group, a 2-sec-butyl-5-pyrimidinyl group, a 4-sec-butyl-5-pyrimidinyl group, a 2-tert-butyl-5-pyrimidinyl group, a 4-tert-butyl-5-pyrimidinyl group, a 2-difluoromethyl-5-pyrimidinyl group, a 4-difluoromethyl-5-pyrimidinyl group, a 2-trifluoromethyl-5-pyrimidinyl group, a 4-trifluoromethyl-5-pyrimidinyl group, a 2-(2,2,2-trifluoroethyl)-5-pyrimidinyl group, a 4-(2,2,2-trifluoroethyl)-5-pyrimidinyl group, a 2-pentafluoroethyl-5-pyrimidinyl group, a 4-pentafluoroethyl-5-pyrimidinyl group, a 2-heptafluoropropyl-5-pyrimidinyl group, a 4-heptafluoropropyl-5-pyrimidinyl group, a 2-heptafluoroisopropyl-5-pyrimidinyl group, a 4-heptafluoroisopropyl-5-pyrimidinyl group, and the like.
Examples of the “5-membered aromatic heterocyclic group” in the compound of the present invention include a 1-pyrazolyl group, a 3-pyrazolyl group, a 4-pyrazolyl group, a 5-pyrazolyl group, a 1-imidazolyl group, a 2-imidazolyl group, a 1-pyrrolyl group, a 2-pyrrolyl group, a 3-pyrrolyl group, a 1-(1,2,4-triazolyl)group, a 1-(1,2,3,4-tetrazolyl)group, a 1-(1,2,3,5-tetrazolyl)group, a 2-furyl group, a 3-furyl group, a 2-thienyl group, a 3-thienyl group, a 3-isoxazolyl group, a 4-isoxazolyl group, a 5-isoxazolyl group, and the like.
Examples of the “5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y” in the compound of the present invention include a 1-pyrazolyl group, a 3-chloro-1-pyrazolyl group, a 3-bromo-1-pyrazolyl group, a 3-nitro-1-pyrazolyl group, a 3-methyl-1-pyrazolyl group, a 3-trifluoromethyl-1-pyrazolyl group, a 4-methyl-1-pyrazolyl group, a 4-chloro-1-pyrazolyl group, a 4-bromo-1-pyrazolyl group, a 4-cyano-1-pyrazolyl group, a 1-methyl-3-pyrazolyl group, a 1-difluoromethyl-3-pyrazolyl group, a 1,5-dimethyl-3-pyrazolyl group, a 1,4-dimethyl-5-pyrazolyl group, a 3,5-dimethyl-1-pyrazolyl group, an 1-imidazolyl group, a 4-trifluoromethyl-1-imidazolyl group, a 1-pyrrolyl group, a 2-fluoro-1-pyrrolyl group, a 3-cyano-1-pyrrolyl group, a 2-methyl-1-pyrrolyl group, a 3-trifluoromethyl-1-pyrrolyl group, a 3-nitro-1-pyrrolyl group, a 2-pyrrolyl group, a 3-fluoro-2-pyrrolyl group, a 4-fluoro-2-pyrrolyl group, a 5-fluoro-2-pyrrolyl group, a 3-chloro-2-pyrrolyl group, a 4-chloro-2-pyrrolyl group, a 5-chloro-2-pyrrolyl group, a 3-bromo-2-pyrrolyl group, a 4-bromo-2-pyrrolyl group, a 5-bromo-2-pyrrolyl group, a 3-iodo-2-pyrrolyl group, a 4-iodo-2-pyrrolyl group, a 5-iodo-2-pyrrolyl group, a 3-cyano-2-pyrrolyl group, a 4-cyano-2-pyrrolyl group, a 5-cyano-2-pyrrolyl group, a 3-nitro-2-pyrrolyl group, a 4-nitro-2-pyrrolyl group, a 5-nitro-2-pyrrolyl group, a 3-methyl-2-pyrrolyl group, a 4-methyl-2-pyrrolyl group, a 5-methyl-2-pyrrolyl group, a 3-ethyl-2-pyrrolyl group, a 4-ethyl-2-pyrrolyl group, a 5-ethyl-2-pyrrolyl group, a 3-propyl-2-pyrrolyl group, a 4-propyl-2-pyrrolyl group, a 5-propyl-2-pyrrolyl group, a 3-isopropyl-2-pyrrolyl group, a 4-isopropyl-2-pyrrolyl group, a 5-isopropyl-2-pyrrolyl group, a 3-tert-butyl-2-pyrrolyl group, a 4-tert-butyl-2-pyrrolyl group, a 5-tert-butyl-2-pyrrolyl group, a 3-difluoromethyl-2-pyrrolyl group, a 4-difluoromethyl-2-pyrrolyl group, a 5-difluoromethyl-2-pyrrolyl group, a 3-trifluoromethyl-2-pyrrolyl group, a 4-trifluoromethyl-2-pyrrolyl group, a 5-trifluoromethyl-2-pyrrolyl group, a 3-pyrrolyl group, a 2-fluoro-3-pyrrolyl group, a 4-fluoro-3-pyrrolyl group, a 5-fluoro-3-pyrrolyl group, a 2-chloro-3-pyrrolyl group, a 4-chloro-3-pyrrolyl group, a 5-chloro-3-pyrrolyl group, a 2-bromo-3-pyrrolyl group, a 4-bromo-3-pyrrolyl group, a 5-bromo-3-pyrrolyl group, a 2-iodo-3-pyrrolyl group, a 4-iodo-3-pyrrolyl group, a 5-iodo-3-pyrrolyl group, a 2-cyano-3-pyrrolyl group, a 4-cyano-3-pyrrolyl group, a 5-cyano-3-pyrrolyl group, a 2-nitro-3-pyrrolyl group, a 4-nitro-3-pyrrolyl group, a 5-nitro-3-pyrrolyl group, a 2-methyl-3-pyrrolyl group, a 4-methyl-3-pyrrolyl group, a 5-methyl-3-pyrrolyl group, a 2-ethyl-3-pyrrolyl group, a 4-ethyl-3-pyrrolyl group, a 5-ethyl-3-pyrrolyl group, a 2-propyl-3-pyrrolyl group, a 4-propyl-3-pyrrolyl group, a 5-propyl-3-pyrrolyl group, a 2-isopropyl-3-pyrrolyl group, a 4-isopropyl-3-pyrrolyl group, a 5-isopropyl-3-pyrrolyl group, a 2-tert-butyl-3-pyrrolyl group, a 4-tert-butyl-3-pyrrolyl group, a 5-tert-butyl-3-pyrrolyl group, a 2-difluoromethyl-3-pyrrolyl group, a 4-difluoromethyl-3-pyrrolyl group, a 5-difluoromethyl-3-pyrrolyl group, a 2-trifluoromethyl-3-pyrrolyl group, a 4-trifluoromethyl-3-pyrrolyl group, a 5-trifluoromethyl-3-pyrrolyl group, a 1-(1,2,4-triazolyl)group, a 3-chloro-1-(1,2,4-triazolyl)group, a 1-(1,2,3,4-tetrazolyl)group, a 1-(1,2,3,5-tetrazolyl)group, a 2-furyl group, a 3-chloro-2-furyl group, a 5-bromo-2-furyl group, a 3-iodo-2-furyl group, a 4-cyano-2-furyl group, a 5-nitro-2-furyl group, a 3-methyl-2-furyl group, a 4-tert-butyl-2-furyl group, a 5-methyl-2-furyl group, a 5-trifluoromethyl-2-furyl group, a 3-furyl group, a 2-fluoro-3-furyl group, a 4-chloro-3-furyl group, a 2-bromo-3-furyl group, a 5-bromo-3-furyl group, a 2-iodo-3-furyl group, a 4-cyano-3-furyl group, a 4-nitro-3-furyl group, a 2-methyl-3-furyl group, a 2-tert-butyl-3-furyl group, a 4-difluoromethyl-3-furyl group, a 5-difluoromethyl-3-furyl group, a 2-trifluoromethyl-3-furyl group, a 4-trifluoromethyl-3-furyl group, a 5-trifluoromethyl-3-furyl group, a 2-thienyl group, a 3-fluoro-2-thienyl group, a 4-fluoro-2-thienyl group, a 5-fluoro-2-thienyl group, a 3-chloro-2-thienyl group, a 4-chloro-2-thienyl group, a 5-chloro-2-thienyl group, a 3-bromo-2-thienyl group, a 4-bromo-2-thienyl group, a 5-bromo-2-thienyl group, a 3-iodo-2-thienyl group, a 4-iodo-2-thienyl group, a 5-iodo-2-thienyl group, a 3-cyano-2-thienyl group, a 4-cyano-2-thienyl group, a 5-cyano-2-thienyl group, a 3-nitro-2-thienyl group, a 4-nitro-2-thienyl group, a 5-nitro-2-thienyl group, a 3-methyl-2-thienyl group, a 4-methyl-2-thienyl group, a 5-methyl-2-thienyl group, a 3-ethyl-2-thienyl group, a 4-ethyl-2-thienyl group, a 5-ethyl-2-thienyl group, a 3-propyl-2-thienyl group, a 4-propyl-2-thienyl group, a 5-propyl-2-thienyl group, a 3-isopropyl-2-thienyl group, a 4-isopropyl-2-thienyl group, a 5-isopropyl-2-thienyl group, a 3-tert-butyl-2-thienyl group, a 4-tert-butyl-2-thienyl group, a 5-tert-butyl-2-thienyl group, a 3-difluoromethyl-2-thienyl group, a 4-difluoromethyl-2-thienyl group, a 5-difluoromethyl-2-thienyl group, a 3-trifluoromethyl-2-thienyl group, a 4-trifluoromethyl-2-thienyl group, a 5-trifluoromethyl-2-thienyl group, a 3-thienyl group, a 2-fluoro-3-thienyl group, a 4-fluoro-3-thienyl group, a 5-fluoro-3-thienyl group, a 2-chloro-3-thienyl group, a 4-chloro-3-thienyl group, a 5-chloro-3-thienyl group, a 2-bromo-3-thienyl group, a 4-bromo-3-thienyl group, a 5-bromo-3-thienyl group, a 2-iodo-3-thienyl group, a 4-iodo-3-thienyl group, a 5-iodo-3-thienyl group, a 2-cyano-3-thienyl group, a 4-cyano-3-thienyl group, a 5-cyano-3-thienyl group, a 2-nitro-3-thienyl group, a 4-nitro-3-thienyl group, a 5-nitro-3-thienyl group, a 2-methyl-3-thienyl group, a 4-methyl-3-thienyl group, a 5-methyl-3-thienyl group, a 2-ethyl-3-thienyl group, a 4-ethyl-3-thienyl group, a 5-ethyl-3-thienyl group, a 2-propyl-3-thienyl group, a 4-propyl-3-thienyl group, a 5-propyl-3-thienyl group, a 2-isopropyl-3-thienyl group, a 4-isopropyl-3-thienyl group, a 5-isopropyl-3-thienyl group, a 2-tert-butyl-3-thienyl group, a 4-tert-butyl-3-thienyl group, a 5-tert-butyl-3-thienyl group, a 2-difluoromethyl-3-thienyl group, a 4-difluoromethyl-3-thienyl group, a 5-difluoromethyl-3-thienyl group, a 2-trifluoromethyl-3-thienyl group, a 4-trifluoromethyl-3-thienyl group, a 5-trifluoromethyl-3-thienyl group, a 2,5-dichloro-3-thienyl group, a 3-isoxazolyl group, a 4-chloro-3-isoxazolyl group, a 5-chloro-3-isoxazolyl group, a 3-bromo-4-isoxazolyl group, a 5-bromo-4-isoxazolyl group, a 3-nitro-5-isoxazolyl group, a 4-nitro-5-isoxazolyl group, a 4-methyl-3-isoxazolyl group, a 5-methyl-3-isoxazolyl group, a 3-trifluoromethyl-4-isoxazolyl group, a 5-trifluoromethyl-4-isoxazolyl group, a m-methyl-5-isoxazolyl group, a 4-methyl-5-isoxazolyl group, and the like.
›MODE FOR CARRYING OUT THE INVENTION · 7 of 73
Examples of the “thienyl group optionally having one or more groups selected from the group Y” in the compound of the present invention include a 2-thienyl group, a 3-fluoro-2-thienyl group, a 4-fluoro-2-thienyl group, a 5-fluoro-2-thienyl group, a 3-chloro-2-thienyl group, a 4-chloro-2-thienyl group, a 5-chloro-2-thienyl group, a 3-bromo-2-thienyl group, a 4-bromo-2-thienyl group, a 5-bromo-2-thienyl group, a 3-iodo-2-thienyl group, a 4-iodo-2-thienyl group, a 5-iodo-2-thienyl group, a 3-cyano-2-thienyl group, a 4-cyano-2-thienyl group, a 5-cyano-2-thienyl group, a 3-nitro-2-thienyl group, a 4-nitro-2-thienyl group, a 5-nitro-2-thienyl group, a 3-methyl-2-thienyl group, a 4-methyl-2-thienyl group, a 5-methyl-2-thienyl group, a 3-ethyl-2-thienyl group, a 4-ethyl-2-thienyl group, a 3-ethyl-2-thienyl group, a 3-propyl-2-thienyl group, a 4-propyl-2-thienyl group, a 5-propyl-2-thienyl group, a 3-isopropyl-2-thienyl group, a 4-isopropyl-2-thienyl group, a 5-isopropyl-2-thienyl group, a 3-tert-butyl-2-thienyl group, a 4-tert-butyl-2-thienyl group, a 5-tert-butyl-2-thienyl group, a 3-difluoromethyl-2-thienyl group, a 4-difluoromethyl-2-thienyl group, a 5-difluoromethyl-2-thienyl group, a 3-trifluoromethyl-2-thienyl group, a 4-trifluoromethyl-2-thienyl group, a 5-trifluoromethyl-2-thienyl group, a 3-thienyl group, a 2-fluoro-3-thienyl group, a 4-fluoro-3-thienyl group, a 5-fluoro-3-thienyl group, a 2-chloro-3-thienyl group, a 4-chloro-3-thienyl group, a 5-chloro-3-thienyl group, a 2-bromo-3-thienyl group, a 4-bromo-3-thienyl group, a 5-bromo-3-thienyl group, a 2-iodo-3-thienyl group, a 4-iodo-3-thienyl group, a 5-iodo-3-thienyl group, a 2-cyano-3-thienyl group, a 4-cyano-3-thienyl group, a 5-cyano-3-thienyl group, a 2-nitro-3-thienyl group, a 4-nitro-3-thienyl group, a 5-nitro-3-thienyl group, a 2-methyl-3-thienyl group, a 4-methyl-3-thienyl group, a 5-methyl-3-thienyl group, a 2-ethyl-3-thienyl group, a 4-ethyl-3-thienyl group, a 5-ethyl-3-thienyl group, a 2-propyl-3-thienyl group, a 4-propyl-3-thienyl group, a 5-propyl-3-thienyl group, a 2-isopropyl-3-thienyl group, a 4-isopropyl-3-thienyl group, a 5-isopropyl-3-thienyl group, a 2-tert-butyl-3-thienyl group, a 4-tert-butyl-3-thienyl group, a 5-tert-butyl-3-thienyl group, a 2-difluoromethyl-3-thienyl group, a 4-difluoromethyl-3-thienyl group, a 5-difluoromethyl-3-thienyl group, a 2-trifluoromethyl-3-thienyl group, a 4-trifluoromethyl-3-thienyl group, a 5-trifluoromethyl-3-thienyl group, a 2,5-dichloro-3-thienyl group, and the like.
Examples of the “pyrrolyl group optionally having one or more groups selected from the group Y” in the compound of the present invention include a 1-pyrrolyl group, a 2-fluoro-1-pyrrolyl group, a 3-cyano-1-pyrrolyl group, a 2-methyl-1-pyrrolyl group, a 3-trifluoromethyl-1-pyrrolyl group, a 3-nitro-1-pyrrolyl group, a 2-pyrrolyl group, a 3-fluoro-2-pyrrolyl group, a 4-fluoro-2-pyrrolyl group, a 5-fluoro-2-pyrrolyl group, a 3-chloro-2-pyrrolyl group, a 4-chloro-2-pyrrolyl group, a 5-chloro-2-pyrrolyl group, a 3-bromo-2-pyrrolyl group, a 4-bromo-2-pyrrolyl group, a 5-bromo-2-pyrrolyl group, a 3-iodo-2-pyrrolyl group, a 4-iodo-2-pyrrolyl group, a 5-iodo-2-pyrrolyl group, a 3-cyano-2-pyrrolyl group, a 4-cyano-2-pyrroyl group, a 5-cyano-2-pyrrolyl group, a 3-nitro-2-pyrrolyl group, a 4-nitro-2-pyrrolyl group, a 5-nitro-2-pyrrolyl group, a 3-methyl-2-pyrrolyl group, a 4-methyl-2-pyrrolyl group, a 5-methyl-2-pyrrolyl group, a 3-ethyl-2-pyrrolyl group, a 4-ethyl-2-pyrrolyl group, a 5-ethyl-2-pyrrolyl group, a 3-propyl-2-pyrrolyl group, a 4-propyl-2-pyrrolyl group, a 5-propyl-2-pyrrolyl group, a 3-isopropyl-2-pyrrolyl group, a 4-isopropyl-2-pyrrolyl group, a 5-isopropyl-2-pyrrolyl group, a 3-tert-butyl-2-pyrrolyl group, a 4-tert-butyl-2-pyrrolyl group, a 5-tert-butyl-2-pyrrolyl group, a 3-difluoromethyl-2-pyrrolyl group, a 4-difluoromethyl-2-pyrrolyl group, a 5-difluoromethyl-2-pyrrolyl group, a 3-trifluoromethyl-2-pyrrolyl group, a 4-trifluoromethyl-2-pyrrolyl group, a 5-trifluoromethyl-2-pyrrolyl group, a 3-pyrrolyl group, a 2-fluoro-3-pyrrolyl group, a 4-fluoro-3-pyrrolyl group, a 5-fluoro-3-pyrrolyl group, a 2-chloro-3-pyrrolyl group, a 4-chloro-3-pyrrolyl group, a 5-chloro-3-pyrrolyl group, a 2-bromo-3-pyrrolyl group, a 4-bromo-3-pyrrolyl group, a 5-bromo-3-pyrrolyl group, a 2-iodo-3-pyrrolyl group, a 4-iodo-3-pyrrolyl group, a 5-iodo-3-pyrrolyl group, a 2-cyano-3-pyrrolyl group, a 4-cyano-3-pyrrolyl group, a 5-cyano-3-pyrrolyl group, a 2-nitro-3-pyrrolyl group, a 4-nitro-3-pyrrolyl group, a 5-nitro-3-pyrrolyl group, a 2-methyl-3-pyrrolyl croup, a 4-methyl-3-pyrrolyl group, a 5-methyl-3-pyrrolyl group, a 2-ethyl-3-pyrrolyl group, a 4-ethyl-3-pyrrolyl group, a 5-ethyl-3-pyrrolyl group, a 2-propyl-3-pyrrolyl group, a 4-propyl-3-pyrrolyl group, a 5-propyl-3-pyrrolyl group, a 2-isopropyl-3-pyrrolyl group, a 4-isopropyl-3-pyrrolyl group, a 5-isopropyl-3-pyrrolyl group, a 2-tert-butyl-3-pyrrolyl group, a 4-tert-butyl-3-pyrrolyl group, a 5-tert-butyl-3-pyrrolyl group, a 2-difluoromethyl-3-pyrrolyl group, a 4-difluoromethyl-3-pyrrolyl group, a 5-difluoromethyl-3-pyrrolyl group, a 2-trifluoromethyl-3-pyrrolyl group, a 4-trifluoromethyl-3-pyrrolyl group, a 5-trifluoromethyl-3-pyrrolyl group, and the like.
Examples of the “pyrazolyl group optionally having one or more groups selected from the group Y” in the compound of the present invention include a 1-pyrazolyl group, a 3-chloro-1-pyrazolyl group, a 3-bromo-1-pyrazoyl group, a 3-nitro-1-pyrazolyl group, a 3-methyl-1-pyrazolyl group, a 3-trifluoromethyl-1-pyrazolyl group, a 4-methyl-1-pyrazolyl group, a 4-chloro-1-pyrazolyl group, a 4-bromo-1-pyrazolyl group, a 4-cyano-1-pyrazolyl group, a 1-methyl-3-pyrazolyl group, a 1-difluoromethyl-3-pyrazolyl group, a 1,5-dimethyl-3-pyrazolyl group, a 1,4-dimethyl-5-pyrazolyl group, a 3,5-dimethyl-1-pyrazolyl group, and the like.
Examples of the “isoxazolyl group optionally having one or more groups selected from the group Y” in the compound of the present invention include a 3-isoxazolyl group, a 4-chloro-3-isoxazolyl group, a 5-chloro-3-isoxazolyl group, a 3-bromo-4-isoxazoyl group, a 5-bromo-4-isoxazolyl group, a 3-nitro-5-isoxazolyl group, a 4-nitro-5-isoxazolyl group, a 4-methyl-3-isoxazolyl group, a 5-methyl-3-isoxazolyl group, a 3-trifluoromethyl-4-isoxazolyl group, a 5-trifluoromethyl-4-isoxazolyl group, a 3-methyl-5-isoxazolyl group, a 4-methyl-5-isoxazolyl group, and the like.
›MODE FOR CARRYING OUT THE INVENTION · 8 of 73
Examples of the “C2-C6 alkylcarbonyl group” in the compound of the present invention include an acetyl group, an ethylcarbonyl group, a propylcarbonyl group, an isopropylcarbonyl group, a butylcarbonyl group, an isobutylcarbonyl group, a sec-butylcarbonyl group, a tert-butylcarbonyl group, a pentylcarbonyl group, a 2,2-dimethylpropylcarbonyl group, a 3-methylbutylcarbonyl group, a pentylcarbonyl group, and the like.
Examples of the “C2-C6 alkylcarbonyl group optionally having one or more halogen atoms” in the compound of the present invention include an acetyl group, an ethylcarbonyl group, a propylcarbonyl group, an isopropylcarbonyl group, a butylcarbonyl group, an isobutylcarbonyl group, a sec-butylcarbonyl group, a tert-butylcarbonyl group, a pentylcarbonyl group, a 2,2-dimethylpropylcarbonyl group, a 3-methylbutylcarbonyl group, a trichloroacetyl group, a difluoroacetyl group, a trifluoroacetyl group, a (2,2,2-trifluoroethyl)carbonyl group, a pentafluoroethylcarbonyl group, a heptafluoropropylcarbonyl group, a heptafluoroisopropylcarbonyl group, and the like.
Examples of the “C2-C5 alkylcarbonyl group” in the compound of the present invention include an acetyl group, an ethylcarbonyl group, a propylcarbonyl group, an isopropylcarbonyl group, a butylcarbonyl group, an isobutylcarbonyl group, a sec-butylcarbonyl group, a tert-butylcarbonyl group, and the like.
Examples of the “C2-C5 alkylcarbonyl group optionally having one or more halogen atoms” in the compound of the present invention include an acetyl group, an ethylcarbonyl group, a propylcarbonyl group, an isopropylcarbonyl group, a butylcarbonyl group, an isobutylcarbonyl group, a sec-butylcarbonyl group, a tert-butylcarbonyl group, a trichloroacetyl group, a difluoroacetyl group, a trifluoroacetyl group, a (2,2,2-trifluoroethyl)carbonyl group, a pentafluoroethylcarbonyl group, a heptafluoropropylcarbonyl group, a heptafluoroisopropylcarbonyl group, and the like.
Examples of the “benzoyl group optionally having one or more groups selected from the group Y” in the compound of the present invention include a benzoyl group, a 2-fluorobenzoyl group, a 3-fluorobenzoyl group, a 4-fluorobenzoyl group, a 2-chlorobenzoyl group, a 3-chlorobenzoyl group, a 4-chlorobenzoyl group, a 2-bromobenzoyl group, a 3-bromobenzoyl group, a 4-bromobenzoyl group, a 2-iodobenzoyl group, a 3-iodobenzoyl group, a 4-iodobenzoyl group, a 2-cyanobenzoyl group, a 3-cyanobenzoyl group, a 4-cyanobenzoyl group, a 2-nitrobenzoyl group, a 3-nitrobenzoyl group, a 4-nitrobenzoyl group, a 2-methylbenzoyl group, a 3-methylbenzoyl group, a 4-methylbenzoyl group, a 2-ethylbenzoyl group, a 3-ethylbenzoyl group, a 4-ethylbenzoyl group, a 2-propylbenzoyl group, a 3-propylbenzoyl group, a 4-propylbenzoyl group, a 2-isopropylbenzoyl group, a 3-isopropylbenzoyl group, a 4-isopropylbenzoyl group, a 2-butylbenzoyl group, a 3-butylbenzoyl group, a 4-butylbenzoyl group, a 2-isobutylbenzoyl group, a 3-isobutylbenzoyl group, a 4-isobutylbenzoyl group, a 2-sec-butylbenzoyl group, a 3-sec-butylbenzoyl group, a 4-sec-butylbenzoyl group, a 2-tert-butylbenzoyl group, a 3-tert-butylbenzoyl group, a 4-tert-butylbenzoyl group, a 2-pentylbenzoyl group, a 3-pentylbenzoyl group, a 4-pentylbenzoyl group, a 2-(2,2-dimethylpropyl)benzoyl group, a 3-(2,2-dimethylpropyl)benzoyl group, a 4-(2,2-dimethylpropyl)benzoyl group, a 2-(3-methylbutyl)benzoyl group, a 3-(3-methylbutyl)benzoyl group, a 4-(3-methylbutyl)benzoyl group, a 2-(2,3-dimethylbutyl)benzoyl group, a 3-(2,3-dimethylbutyl)benzoyl group, a 4-(2,3-dimethylbutyl)benzoyl group, a 2-(3,3-dimethylbutyl)benzoyl group, a 3-(3,3-dimethylbutyl)benzoyl group, a 4-(3,3-dimethylbutyl)benzoyl group, a 2-hexylbenzoyl group, a 3-hexylbenzoyl group, a 4-hexylbenzoyl group, a 2-trichloromethylbenzoyl group, a 3-trichloromethylbenzoyl group, a 4-trichloromethylbenzoyl group, a 2-difluoromethylbenzoyl group, a 3-difluoromethylbenzoyl group, a 4-difluoromethylbenzoyl group, a 2-trifluoromethylbenzoyl group, a 3-trifluoromethylbenzoyl group, a 4-trifluoromethylbenzoyl group, a 2-(2,2,2-trifluoroethyl)benzoyl group, a 3-(2,2,2-trifluoromethyl)benzoyl group, a 4-(2,2,2-trifluoroethyl)benzoyl group, a 2-pentafluoroethylbenzoyl group, a 3-pentafluoroethylbenzoyl group, a 4-pentafluoroethylbenzoyl group, a 2-heptafluoropropylbenzoyl group, a 3-heptafluoropropylbenzoyl group, a 4-heptafluoropropylbenzoyl group, a 2-heptafluoroisopropylbenzoyl group, a 3-heptafluoroisopropylbenzoyl group, a 4-heptafluoroisopropylbenzoyl group, a 2-methoxybenzoyl group, a 3-methoxybenzoyl group, a 4-methoxybenzoyl group, a 2-ethoxybenzoyl group, a 3-ethoxybenzoyl group, a 4-ethoxybenzoyl group, a 2-propoxybenzoyl group, a 3-propoxybenzoyl group, a 4-propoxybenzoyl group, a 2-isopropoxybenzoyl group, a 3-isopropoxybenzoyl group, a 4-isopropoxybenzoyl group, a 2-butoxybenzoyl group, a 3-butoxybenzoyl group, a 4-butoxybenzoyl group, a 2-isobutoxybenzoyl group, a 3-isobutoxybenzoyl group, a 4-isobutoxybenzoyl group, a 2-sec-butoxybenzoyl group, a 3-sec-butoxybenzoyl group, a 4-sec-butoxybenzoyl group, a 2-tert-butoxybenzoyl group, a 3-tert-butoxybenzoyl group, a 4-tert-butoxybenzoyl group, a 2-pentyloxybenzoyl group, a 3-pentyloxybenzoyl group, a 4-pentyloxybenzoyl group, a 2-(2,2-dimethylpropoxyl)benzoyl group, a 3-(2,2-dimethylpropoxyl)benzoyl group, a 4-(2,2-dimethylpropoxyl)benzoyl group, a 2-pentafluoroethoxybenzoyl group, a 3-pentafluoroethoxybenzoyl group, a 4-pentafluoroethoxybenzoyl group, a 2-heptafluoropropoxybenzoyl group, a 3-heptafluoropropoxybenzoyl group, a 4-heptafluoropropoxybenzoyl group, a 2-heptafluoroisopropoxybenzoyl group, a 3-heptafluoroisopropoxybenzoyl group, a 4-heptafluoroisopropoxybenzoyl group, a 2-trifluoromethoxybenzoyl group, a 3-trifluoromethoxybenzoyl group, a 4-trifluoromethoxybenzoyl group, and the like.
Examples of the “C2-C6 alkoxycarbonyl group” in the compound of the present invention include an methoxycarbonyl group, an ethoxycarbonyl group, a propoxycarbonyl group, an isopropoxycarbonyl group, a butoxycarbonyl group, an isobutoxycarbonyl group, a sec-butoxycarbonyl group, a tert-butoxycarbonyl group, a pentyloxycarbonyl group, a 2,2-dimethylpropoxycarbonyl group, a 3-methylbutoxycarbonyl group, and the like.
›MODE FOR CARRYING OUT THE INVENTION · 9 of 73
Examples of the “C2-C5 alkoxycarbonyl group” in the compound of the present invention include a methoxycarbonyl group, an ethoxycarbonyl group, a propoxycarbonyl group, an isopropoxycarbonyl group, a butoxycarbonyl group, an isobutoxycarbonyl group, a sec-butoxycarbonyl group, and a tert-butoxycarbonyl group.
Examples of the “C2-C4 alkoxycarbonyl group” in the compound of the present invention include a methoxycarbonyl group, an ethoxycarbonyl group, a propoxycarbonyl group, and an isopropoxycarbonyl group.
Examples of the “C1-C4 alkylsulfonyl group” in the compound of the present invention include a methylsulfonyl group, an ethylsulfonyl group, a propylsulfonyl group, an isopropylsulfonyl group, a butylsulfonyl group, an isobutylsulfonyl group, a sec-butylsulfonyl group, and a tert-butylsulfonyl group.
Examples of the “C1-C4 alkylsulfonyl group optionally having one or more halogen atoms” in the compound of the present invention include a methylsulfonyl group, an ethylsulfonyl group, a propylsulfonyl group, an isopropylsulfonyl group, a butylsulfonyl group, an isobutylsulfonyl group, a sec-butylsulfonyl group, a tert-butylsulfonyl group, a trichloromethylsulfonyl group, a difluoromethylsulfonyl group, a trifluoromethylsulfonyl group, a 2,2,2-trifluoroethylsulfonyl group, and the like.
Examples of the “C1-C6 alkylsulfonyl group” in the compound of the present invention include a methylsulfonyl group, an ethylsulfonyl group, a propylsulfonyl group, an isopropylsulfonyl group, a butylsulfonyl group, an isobutylsulfonyl group, a sec-butylsulfonyl group, a tert-butylsulfonyl group, a pentylsulfonyl group, a 2,2-dimethylpropylsulfonyl group, a 3-methylbutylsulfonyl group, a 2,3-dimethylbutylsulfonyl Group, a 3,3-dimethylbutylsulfonyl group, a hexylsulfonyl group, and the like.
Examples of the “C1-C6 alkylsulfonyl group optionally having one or more halogen atoms” in the compound of the present invention include a methylsulfonyl group, an ethylsulfonyl group, a propylsulfonyl group, an isopropylsulfonyl group, a butylsulfonyl group, an isobutylsulfonyl group, a sec-butylsulfonyl group, a tert-butylsulfonyl group, a pentylsulfonyl group, a 2,2-dimethylpropylsulfonyl group, a 3-methylbutylsulfonyl group, a 2,3-dimethylbutylsulfonyl group, a 3,3-dimethylbutylsulfonyl group, a hexylsulfonyl group, a trichloromethylsulfonyl group, a difluoromethylsulfonyl group, a trifluoromethylsulfonyl group, a 2,2,2-trifluoroethylsulfonyl group, a pentafluoroethylsulfonyl group, a heptafluoropropylsulfonyl group, a heptafluoroisopropylsulfonyl group, and the like.
Examples of the “phenylsulfonyl group optionally having one or more groups selected from the group Y” in the compound of the present invention include a 2-fluorophenylsulfonyl group, a 3-chlorophenylsulfonyl group, a 4-chlorophenylsulfonyl group, a 2-iodophenylsulfonyl group, a 3-cyanophenylsulfonyl group, a 4-nitrophenylsulfonyl group, a 2-methylphenylsulfonyl group, a 4-methylphenylsulfonyl group, a 4-tert-butylphenylsulfonyl group, a 4-difluoromethylphenylsulfonyl group, a 2-trifluoromethylphenylsulfonyl group, a 2-(2,2,2-trifluoroethyl)phenylsulfonyl group, a 4-pentafluoroethylphenylsulfonyl group, a 4-heptafluoroisopropylphenylsulfonyl group, a 2-methoxyphenylsulfonyl group, a 3-difluoromethoxyphenylsulfonyl group, a 4-difluoromethoxyphenylsulfonyl group, a 2-trifluoromethoxyphenylsulfonyl group, a 4-(2,2,2-trifluoroethoxy)phenylsulfonyl group, and the like.
Examples of the “C7-C9 phenylalkylsulfonyl group” in the compound of the present invention include a benzylsulfonyl group, a 1-phenylethylsulfonyl group, a 2-phenylethylsulfonyl group, a 1-phenylpropylsulfonyl group, a 2-phenylpropylsulfonyl group, a 3-phenylpropylsulfonyl group, a 1-methyl-1-phenylethylsulfonyl group, and the like.
Examples of the “C7-C9 phenylalkylsulfonyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y” in the compound of the present invention include a benzylsulfonyl group, a 2-fluorobenzylsulfonyl group, a 3-chlorobenzylsulfonyl group, a 4-bromobenzylsulfonyl group, a 2-cyanobenzylsulfonyl group, a 3-nitrobenzylsulfonyl group, a 3-methoxybenzylsulfonyl group, a 4-trifluoromethoxybenzylsulfonyl group, a 1-(3-chlorophenyl)ethylsulfonyl group, a 2-(4-bromophenyl)ethylsulfonyl group, a 1-(2-cyanophenyl)propylsulfonyl group, a 2-(3-nitrophenyl)propylsulfonyl group, a 3-(3-methoxyphenyl)propylsulfonyl group, a 1-methyl-1-(4-trifluoromethoxyphenyl)ethylsulfonyl group, and the like.
Examples of the “benzylsulfonyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y” in the compound of the present invention include a benzylsulfonyl group, a 2-fluorobenzylsulfonyl group, a 3-chlorobenzylsulfonyl group, a 4-bromobenzylsulfonyl group, a 2-cyanobenzylsulfonyl group, a 3-nitrobenzylsulfonyl group, a 3-methoxybenzylsulfonyl group, a 4-trifluoromethoxybenzylsulfonyl group, and the like.
Examples of the “C1-C6 alkoxy group” in the compound of the present invention include a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a butoxy group, an isobutoxy group, a sec-butoxy group, a tert-butoxy group, a pentyloxy group, a 2,2-dimethylpropoxy group, a 3-methylbutoxy group, a 2,3-dimethylbutoxy group, a 3,3-dimethylbutoxy group, a hexyloxy group, and the like.
Examples of the “C1-C6 alkoxy group optionally having one or more halogen atoms” in the compound of the present invention include a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a butoxy group, an isobutoxy group, a sec-butoxy group, a tert-butoxy group, a pentyloxy group, a 2,2-dimethylpropoxy group, a 3-methylbutoxy group, a 2,3-dimethylbutoxy group, a 3,3-dimethylbutoxy group, a hexyloxy group, a trichloromethoxy group, a difluoromethoxy group, a trifluoromethoxy group, a 2,2,2-trifluoroethoxy group, a pentafluoroethoxy group, a heptafluoropropoxy group, a heptafluoroisopropoxy group, and the like.
Examples of the compound of the present invention include the following compounds.
›MODE FOR CARRYING OUT THE INVENTION · 10 of 73
A compound represented by Formula (1) wherein R 1 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents a nitro group;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkenyl group;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkenyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkynyl group;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkynyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a phenyl group;
a compound represented by Formula (1) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a 6-membered aromatic heterocyclic group;
a compound represented by Formula (1) wherein R 1 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a 5-membered aromatic heterocyclic group;
a compound represented by Formula (1) wherein R 1 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a carboxy group;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a benzoyl group;
a compound represented by Formula (1) wherein R 1 represents a benzoyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a aminocarbonyl group;
a compound represented by Formula (1) wherein R 1 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents —S(O) 2 NR 7 R 11 ;
a compound represented by Formula (1) wherein R 1 represents —OR 11 ;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 11 ;
a compound represented by Formula (1) wherein R 1 represents —SF 5 ;
a compound represented by Formula (1) wherein R 1 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a C2-C4 alkenyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a C2-C4 alkynyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a pyridyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a pyrimidinyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a thienyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a pyrrolyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a C2-C5 alkylcarbonyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a cyano group;
a compound represented by Formula (1) wherein R 2 represents a nitro group;
a compound represented by Formula (1) wherein R 2 represents a C1-C6 alkyl group;
a compound represented by Formula (1) wherein R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkenyl group;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkenyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkynyl group;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkynyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a phenyl group;
a compound represented by Formula (1) wherein R 2 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a 6-membered aromatic heterocyclic group;
a compound represented by Formula (1) wherein R 2 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a 5-membered aromatic heterocyclic group;
a compound represented by Formula (1) wherein R 2 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkylcarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group optionally having one or more groups selected from the group Y;
›MODE FOR CARRYING OUT THE INVENTION · 11 of 73
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a aminocarbonyl group;
a compound represented by Formula (1) wherein R 2 represents —NR 12 R 13 ;
a compound represented by Formula (1) wherein R 2 represents —S(O) 2 NR 7 R 11 ;
a compound represented by Formula (1) wherein R 2 represents —OR 13 ;
a compound represented by Formula (1) wherein R 2 represents —S(O) m R 13 ;
a compound represented by Formula (1) wherein R 2 represents —SF 5 ;
a compound represented by Formula (1) wherein R 2 represents a C1-C4 alkyl group;
a compound represented by Formula (1) wherein R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a C2-C4 alkenyl group;
a compound represented by Formula (1) wherein R 2 represents a C2-C4 alkenyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a C2-C4 alkynyl group;
a compound represented by Formula (1) wherein R 2 represents a C2-C4 alkynyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a pyridyl group;
a compound represented by Formula (1) wherein R 2 represents a pyridyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a pyrimidinyl group;
a compound represented by Formula (1) wherein R 2 represents a pyrimidinyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a thienyl group;
a compound represented by Formula (1) wherein R 2 represents a thienyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a pyrrolyl group;
a compound represented by Formula (1) wherein R 2 represents a pyrrolyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a C2-C5 alkylcarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a C2-C5 alkylcarbonyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a C2-C4 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a halogen atom;
a compound represented by Formula (1) wherein R 3 represents a cyano group;
a compound represented by Formula (1) wherein R 3 represents a nitro group;
a compound represented by Formula (1) wherein R 3 represents a C1-C6 alkyl group;
a compound represented by Formula (1) wherein R 3 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkenyl group;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkenyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkynyl group;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkynyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 3 represents a phenyl group;
a compound represented by Formula (1) wherein R 3 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a 6-membered aromatic heterocyclic group;
a compound represented by Formula (1) wherein R 3 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a 5-membered aromatic heterocyclic group;
a compound represented by Formula (1) wherein R 3 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a carboxy group;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkylcarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 represents a benzoyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a aminocarbonyl group;
a compound represented by Formula (1) wherein R 3 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 3 represents —S(O) 2 NR 7 R 11 ;
a compound represented by Formula (1) wherein R 3 represents —OR 11 ;
a compound represented by Formula (1) wherein R 3 represents —S(O) m R 11 ;
a compound represented by Formula (1) wherein R 3 represents —SF 5 ;
a compound represented by Formula (1) wherein R 3 represents a C1-C4 alkyl group;
a compound represented by Formula (1) wherein R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 represents a C2-C4 alkenyl group;
a compound represented by Formula (1) wherein R 3 represents a C2-C4 alkenyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 represents a C2-C4 alkynyl group;
a compound represented by Formula (1) wherein R 3 represents a C2-C4 alkynyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 represents a pyridyl group;
a compound represented by Formula (1) wherein R 3 represents a pyridyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a pyrimidinyl group;
a compound represented by Formula (1) wherein R 3 represents a pyrimidinyl group optionally having one or more groups selected from the group Y;
›MODE FOR CARRYING OUT THE INVENTION · 12 of 73
a compound represented by Formula (1) wherein R 3 represents a thienyl group;
a compound represented by Formula (1) wherein R 3 represents a thienyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a pyrrolyl group;
a compound represented by Formula (1) wherein R 3 represents a pyrrolyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a pyrazolyl group;
a compound represented by Formula (1) wherein R 3 represents a pyrazolyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a C2-C5 alkylcarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a C2-C5 alkylcarbonyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 represents a C2-C4 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a halogen atom;
a compound represented by Formula (1) wherein R 4 represents a cyano group;
a compound represented by Formula (1) wherein R 4 represents a nitro group;
a compound represented by Formula (1) wherein R 4 represents a C1-C6 alkyl group;
a compound represented by Formula (1) wherein R 4 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkenyl group;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkenyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkynyl group;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkynyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 4 represents a phenyl group;
a compound represented by Formula (1) wherein R 4 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a 6-membered aromatic heterocyclic group;
a compound represented by Formula (1) wherein R 4 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a 5-membered aromatic heterocyclic group;
a compound represented by Formula (1) wherein R 4 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a carboxy group;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkylcarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 4 represents a benzoyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents an aminocarbonyl group;
a compound represented by Formula (1) wherein R 4 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 4 represents —S(O) 2 NR 7 R 11 ;
a compound represented by Formula (1) wherein R 4 represents —OR 11 ;
a compound represented by Formula (1) wherein R 4 represents —S(O) m R 11 ;
a compound represented by Formula (1) wherein R 4 represents —SF 5 ;
a compound represented by Formula (1) wherein R 4 represents a C1-C4 alkyl group;
a compound represented by Formula (1) wherein R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 4 represents a C2-C4 alkenyl group;
a compound represented by Formula (1) wherein R 4 represents a C2-C4 alkenyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 4 represents a C2-C4 alkynyl group;
a compound represented by Formula (1) wherein R 4 represents a C2-C4 alkynyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 4 represents a pyridyl group;
a compound represented by Formula (1) wherein R 4 represents a pyridyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a pyrimidinyl group;
a compound represented by Formula (1) wherein R 4 represents a pyrimidinyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a thienyl group;
a compound represented by Formula (1) wherein R 4 represents a thienyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a pyrrolyl group;
a compound represented by Formula (1) wherein R 4 represents a pyrrolyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a C2-C5 alkylcarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a C2-C5 alkylcarbonyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 4 represents a C2-C4 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 5 represents a cyano group;
a compound represented by Formula (1) wherein R 5 represents a nitro group;
a compound represented by Formula (1) wherein R 5 represents a C1-C6 alkyl group;
a compound represented by Formula (1) wherein R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
›MODE FOR CARRYING OUT THE INVENTION · 13 of 73
a compound represented by Formula (1) wherein R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 5 represents —S(O) 2 NR 7 R 11 ;
a compound represented by Formula (1) wherein R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 5 represents a phenyl group;
a compound represented by Formula (1) wherein R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 5 represents a 6-membered aromatic heterocyclic group;
a compound represented by Formula (1) wherein R 5 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 5 represents a 5-membered aromatic heterocyclic group;
a compound represented by Formula (1) wherein R 5 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 5 represents a C1-C4 alkyl group;
a compound represented by Formula (1) wherein R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 5 represents a C2-C5 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 5 represents a pyrrolyl group;
a compound represented by Formula (1) wherein R 5 represents a pyrrolyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R-represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R: represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y, and R 3 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
›MODE FOR CARRYING OUT THE INVENTION · 14 of 73
a compound represented by Formula (1) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R-represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a thienyl group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 1 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents —OR 14 ;
a compound represented by Formula C1) wherein R 1 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a carboxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a carboxy group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents a carboxy group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a carboxy group, and R 5 represents carboxy group;
a compound represented by Formula (1) wherein R 1 represents a carboxy group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a carboxy group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents a carboxy group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a carboxy group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a carboxy group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group which may have optionally one or more halogen atoms, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a carboxy group;
›MODE FOR CARRYING OUT THE INVENTION · 15 of 73
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a C2-C5 alkoxycarbonyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R-represents a C2-C6 alkoxycarbonyl group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkoxycarbonyl group, and R 5 represents NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkoxycarbonyl group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkoxycarbonyl group, and R 3 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents an aminocarbonyl group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents an aminocarbonyl group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents an aminocarbonyl group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 1 represents an aminocarbonyl group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents an aminocarbonyl group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents an aminocarbonyl group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents an aminocarbonyl group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents an aminocarbonyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents —NR 11 R 12 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents —OR 11 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents —OR 11 , and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents —OR 11 , and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents —OR 11 , and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 1 represents —OR 11 , and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents —OR 11 , and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents —OR 11 , and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents —OR 11 , and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents —OR 11 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents —S(O) n R 11 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 11 , and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 11 , and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 11 , and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 11 , and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 11 , and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 11 , and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 11 , and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 11 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents —SF 5 , and R 5 represents a hydrogen atom;
›MODE FOR CARRYING OUT THE INVENTION · 16 of 73
a compound represented by Formula (1) wherein R 1 represents —SF 5 , and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents —SF 5 , and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents —SF 5 , and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 1 represents —SF 5 , and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents —SF 5 , and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents —SF 5 , and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents —SF 5 , and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents —SF 5 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (12 wherein R 1 represents a C1-C4 alkyl group optionally having one cr more halogen atoms, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 1 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R-represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a pyrrolyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a C2-C5 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a halogen atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a halogen atom, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a halogen atom, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a halogen atom, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents a halogen atom, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a halogen atom, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents a halogen atom, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents a halogen atom, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a halogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a carboxy group;
›MODE FOR CARRYING OUT THE INVENTION · 17 of 73
a compound represented by Formula (1) wherein R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a 6-membered aromatic heterocyclic group which may have optionally one or more groups selected from the group Y, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents —NR 11 R 12 ;
›MODE FOR CARRYING OUT THE INVENTION · 18 of 73
a compound represented by Formula (1) wherein R 2 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a carboxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a carboxy group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a carboxy group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a carboxy group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents a carboxy group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a carboxy group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents a carboxy group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents a carboxy group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a carboxy group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group optionally having one or more groups selected from the group Y, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group optionally having one or more groups selected from the group Y, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group optionally having one or more groups selected from the group Y, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group optionally having one or more groups selected from the group Y, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group optionally having one or more groups selected from the group Y, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group optionally having one or more groups selected from the group Y, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a C2-C6 alkoxycarbonyl group;
›MODE FOR CARRYING OUT THE INVENTION · 19 of 73
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkoxycarbonyl group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkoxycarbonyl group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents an aminocarbonyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents an aminocarbonyl group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents an aminocarbonyl group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents an aminocarbonyl group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents an aminocarbonyl group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents an aminocarbonyl group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents an aminocarbonyl group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents an aminocarbonyl group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents an aminocarbonyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents —NR 12 R 13 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents —NR 12 R 13 , and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents —NR 12 R 13 , and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents —NR 12 R 13 , and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents —NR 12 R 13 , and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents —NR 12 R 13 , and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents —NR 12 R 13 , and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents —NR 12 R 13 , and R 5 represents phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents —NR 12 R 13 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents —S(O) 2 NR 7 R 11 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents —S(O) 2 NR 7 R 11 , and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents —S(O) 2 NR 7 R 11 , and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents —S(O) 2 NR 7 R 11 , and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents —S(O) 2 NR 7 R 11 , and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents —S(O) 2 NR 7 R 11 , and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents —S(O) 2 NR 7 R 11 , and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents —S(O) 2 NR 7 R 11 , and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents —S(O) 2 NR 7 R 11 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents —OR 13 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents —OR 13 , and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents —OR 13 , and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents —OR 13 , and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents —OR 13 , and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents —OR 13 , and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents —OR 13 , and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents —OR 13 , and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents —OR 13 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents —S(O) m R 13 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents —S(O) m R 13 , and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents —S(O) m R 13 , and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents —S(O) m R 13 , and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents —S(O) m R 13 , and R 5 represents a C2-C6 alkoxycarbonyl group;
›MODE FOR CARRYING OUT THE INVENTION · 20 of 73
a compound represented by Formula (1) wherein R 2 represents —S(O) m R 13 , and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents —S(O) m R 13 , and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents —S(O) m R 13 , and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents —S(O) m R 13 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents —SF 5 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents —SF 5 , and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents —SF 5 , and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents —SF 5 , and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents —SF 5 , and R 5 represents C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents —SF 5 , and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents —SF 5 , and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents —SF 5 , and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents —SF 5 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C1-C4 alkyl group which may have optionally one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a pyridyl group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a pyrimidinyl group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a thienyl group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a C2-C5 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a pyrrolyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents —S(O) 2 NR 7 R 11 ,
a compound represented by Formula (1) wherein R 2 represents a nitro group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 3 represents a halogen atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a halogen atom, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 3 represents a halogen atom, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
›MODE FOR CARRYING OUT THE INVENTION · 21 of 73
a compound represented by Formula (1) wherein R 3 represents a halogen atom, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 3 represents a halogen atom, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a halogen atom, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 3 represents a halogen atom, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 3 represents a halogen atom, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a halogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 represents a carboxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a carboxy group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 3 represents a carboxy group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 3 represents a carboxy group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 3 represents a carboxy group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a carboxy group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 3 represents a carboxy group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 3 represents a carboxy group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a carboxy group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group x;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkoxycarbonyl group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkoxycarbonyl group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 represents an aminocarbonyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents an aminocarbonyl group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 3 represents an aminocarbonyl group, and R 5 represents a CL-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 3 represents an aminocarbonyl group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 3 represents an aminocarbonyl group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents an aminocarbonyl group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 3 represents an aminocarbonyl group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 3 represents an aminocarbonyl group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents an aminocarbonyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
›MODE FOR CARRYING OUT THE INVENTION · 22 of 73
a compound represented by Formula (1) wherein R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a C2-C4 alkenyl group optionally having one or more halogen atoms, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a C2-C4 alkynyl group optionally having one or more halogen atoms, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a pyridyl group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents —NR 11 R 12 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents —OR 14 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula 1) wherein R 3 represents a hydrogen atom, and R 5 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a pyrrolyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 4 represents a halogen atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a halogen atom, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 4 represents a halogen atom, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 4 represents a halogen atom, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 4 represents a halogen atom, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a halogen atom, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 4 represents a halogen atom, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 4 represents a halogen atom, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a halogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 4 represents a carboxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a carboxy group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 4 represents a carboxy group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 4 represents a carboxy group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 4 represents a carboxy group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a carboxy group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 4 represents a carboxy group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 4 represents a carboxy group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a carboxy group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkoxycarbonyl group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkoxycarbonyl group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
›MODE FOR CARRYING OUT THE INVENTION · 23 of 73
a compound represented by Formula (1) wherein R 4 represents an aminocarbonyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents an aminocarbonyl group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 4 represents an aminocarbonyl group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 4 represents an aminocarbonyl group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 4 represents an aminocarbonyl group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents an aminocarbonyl group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 4 represents an aminocarbonyl group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 4 represents an aminocarbonyl group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents an aminocarbonyl group, and R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 4 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 4 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 4 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 4 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 4 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a phenyl group optionally having one or more groups selected from the group Y, and R 3 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents —OR 11 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a halogen atom;
a compound represented by Formula C1) wherein R 4 represents a hydrogen atom, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a pyrrolyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a C2-C4 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents —S(O) 2 NR 7 R 11 ;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, and R 5 represents a hydrogen atom;
›MODE FOR CARRYING OUT THE INVENTION · 24 of 73
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 represents a trifluoromethyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a trifluoromethyl group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 3 represents a trifluoromethyl group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 3 represents a trifluoromethyl group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 3 represents a trifluoromethyl group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a trifluoromethyl group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 3 represents a trifluoromethyl group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 3 represents a trifluoromethyl group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 represents a trifluoromethyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 4 represents a trifluoromethyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a trifluoromethyl group, and R 5 represents a halogen atom;
a compound represented by Formula (1) wherein R 4 represents a trifluoromethyl group, and R 5 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 4 represents a trifluoromethyl group, and R 5 represents a carboxy group;
a compound represented by Formula (1) wherein R 4 represents a trifluoromethyl group, and R 5 represents a C2-C6 alkoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a trifluoromethyl group, and R 5 represents —NR 11 R 12 ;
a compound represented by Formula (1) wherein R 4 represents a trifluoromethyl group, and R 5 represents —OR 14 ;
a compound represented by Formula (1) wherein R 4 represents a trifluoromethyl group, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 4 represents a trifluoromethyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R=represents a halogen atom, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 3 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a carboxy group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a trifluoromethyl group;
›MODE FOR CARRYING OUT THE INVENTION · 25 of 73
a compound represented by Formula (1) wherein R 1 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents an aminocarbonyl group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents —OR 11 , and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents —S(O) n R 11 , and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents —SF 5 , and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a halogen atom, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a carboxy group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group optionally having one or more groups selected from the group Y, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents an aminocarbonyl group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents —NR 12 R 13 , and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents —S(O) 2 NR 7 R 11 , and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents —OR 13 , and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents —S(O) m R 13 , and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents —SF 5 , and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 3 represents a halogen atom, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 3 represents a carboxy group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 3 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 3 represents an aminocarbonyl group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 4 represents a halogen atom, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 4 represents a carboxy group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 4 represents a C2-C6 alkoxycarbonyl group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 4 represents a aminocarbonyl group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a fluorine atom;
a compound represented by Formula (1) wherein R 2 represents a fluorine atom;
a compound represented by Formula (1) wherein R 3 represents a fluorine atom;
a compound represented by Formula (1) wherein R 4 represents a fluorine atom;
a compound represented by Formula (1) wherein R 5 represents a fluorine atom;
a compound represented by Formula (1) wherein R 1 represents a chlorine atom;
a compound represented by Formula (1) wherein R 2 represents a chlorine atom;
a compound represented by Formula (1) wherein R 3 represents a chlorine atom;
a compound represented by Formula (1) wherein R 4 represents a chlorine atom;
a compound represented by Formula (1) wherein R 5 represents a chlorine atom;
a compound represented by Formula (1) wherein R 1 represents a bromine atom;
a compound represented by Formula (1) wherein R 2 represents a bromine atom;
a compound represented by Formula (1) wherein R 3 represents a bromine atom;
a compound represented by Formula (1) wherein R 4 represents a bromine atom;
a compound represented by Formula (1) wherein R 3 represents a bromine atom;
›MODE FOR CARRYING OUT THE INVENTION · 26 of 73
a compound represented by Formula (1) wherein R 1 represents a iodine atom;
a compound represented by Formula (1) wherein R 2 represents a iodine atom;
a compound represented by Formula (1) wherein R 3 represents a iodine atom;
a compound represented by Formula (1) wherein R 4 represents a iodine atom;
a compound represented by Formula (1: wherein R 5 represents a iodine atom;
a compound represented by Formula (1) wherein R 1 represents a methyl group;
a compound represented by Formula (1) wherein R 2 represents a methyl group;
a compound represented by Formula (1) wherein R 3 represents a methyl group;
a compound represented by Formula (1) wherein R 4 represents a methyl group;
a compound represented by Formula (1) wherein R 5 represents a methyl group;
a compound represented by Formula (1) wherein R 1 represents an ethyl group;
a compound represented by Formula (1) wherein R 2 represents an ethyl group;
a compound represented by Formula (1) wherein R 3 represents an ethyl group;
a compound represented by Formula (1) wherein R 4 represents an ethyl group;
a compound represented by Formula (1) wherein R 5 represents an ethyl group;
a compound represented by Formula (1) wherein R 1 represents an isopropyl group;
a compound represented by Formula (1) wherein R 2 represents an isopropyl group;
a compound represented by Formula (1) wherein R 3 represents an isopropyl group;
a compound represented by Formula (1) wherein R 4 represents an isopropyl group;
a compound represented by Formula (1) wherein R 5 represents an isopropyl group;
a compound represented by Formula (1) wherein R 1 represents a tert-butyl group;
a compound represented by Formula (1) wherein R 2 represents a tert-butyl group;
a compound represented by Formula (1) wherein R 3 represents a tert-butyl group;
a compound represented by Formula (1) wherein R 4 represents a tert-butyl group;
a compound represented by Formula (1) wherein R 5 represents a tert-butyl group;
a compound represented by Formula (1) wherein R 1 represents a difluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a difluoromethyl group;
a compound represented by Formula (1) wherein R 3 represents a difluoromethyl group;
a compound represented by Formula (1) wherein R 4 represents a difluoromethyl group;
a compound represented by Formula (1) wherein R 5 represents a difluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 3 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 4 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a 2,2,2-trifluoroethyl group;
a compound represented by Formula (1) wherein R 2 represents a 2,2,2-trifluoroethyl group;
a compound represented by Formula (1) wherein R 3 represents a 2,2,2-trifluoroethyl group;
a compound represented by Formula (1) wherein R 4 represents a 2,2,2-trifluoroethyl group;
a compound represented by Formula (1) wherein R 5 represents a 2,2,2-trifluoroethyl group;
a compound represented by Formula (1) wherein R 1 represents a pentafluoroethyl group;
a compound represented by Formula (1) wherein R 2 represents a pentafluoroethyl group;
a compound represented by Formula (1) wherein R 3 represents a pentafluoroethyl group;
a compound represented by Formula (1) wherein R 4 represents a pentafluoroethyl group;
a compound represented by Formula (1) wherein R 5 represents a pentafluoroethyl group;
a compound represented by Formula (1) wherein R 1 represents a heptafluoropropyl group;
a compound represented by Formula (1) wherein R 2 represents a heptafluoropropyl group;
a compound represented by Formula (1) wherein R 3 represents a heptafluoropropyl group;
a compound represented by Formula (1) wherein R 4 represents a heptafluoropropyl group;
a compound represented by Formula (1) wherein R 5 represents a heptafluoropropyl group;
a compound represented by Formula (1) wherein R 1 represents a heptafluoroisopropyl group;
a compound represented by Formula (1) wherein R 2 represents a heptafluoroisopropyl group;
a compound represented by Formula (1) wherein R 3 represents a heptafluoroisopropyl group;
a compound represented by Formula (1) wherein R 4 represents a heptafluoroisopropyl group;
a compound represented by Formula (1) wherein R 5 represents a heptafluoroisopropyl group;
a compound represented by Formula (1) wherein R 1 represents a methoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a methoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a methoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a methoxycarbonyl group;
a compound represented by Formula (1) wherein R 5 represents a methoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents an ethoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents an ethoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents an ethoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents an ethoxycarbonyl group;
a compound represented by Formula (1) wherein R 5 represents an ethoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a difluoromethoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a difluoromethoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a difluoromethoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a difluoromethoxycarbonyl group;
a compound represented by Formula (1) wherein R 5 represents a difluoromethoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a trifluoroethoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a trifluoroethoxycarbonyl group;
›MODE FOR CARRYING OUT THE INVENTION · 27 of 73
a compound represented by Formula (1) wherein R 3 represents a trifluoromethoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a trifluoromethoxycarbonyl group;
a compound represented by Formula (1) wherein R 5 represents a trifluoromethoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a 2,2,2-trifluoroethoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a 2,2,2-trifluoroethoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a 2,2,2-trifluoroethoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a 2,2,2-trifluoroethoxycarbonyl group;
a compound represented by Formula (1) wherein R 5 represents a 2,2,2-trifluoroethoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a hydroxy group;
a compound represented by Formula (1) wherein R 1 represents a methoxy group;
a compound represented by Formula (1) wherein R 1 represents an amino group;
a compound represented by Formula (1) wherein R 1 represents a dimethylamino group;
a compound represented by Formula C1) wherein R 1 represents a 2-thienyl group;
a compound represented by Formula (1) wherein R 2 represents a 2-chlorophenyl croup;
a compound represented by Formula (1) wherein R 2 represents a 3-chlorophenyl group;
a compound represented by Formula (1) wherein R 2 represents a 4-chlorophenyl group;
a compound represented by Formula (1) wherein R 2 represents a 4-trifluoromethylphenyl group;
a compound represented by Formula (1) wherein R 2 represents a 2-pyridyl group;
a compound represented by Formula (1) wherein R 2 represents a 3-pyridyl group;
a compound represented by Formula (1) wherein R 2 represents a 4-pyridyl group;
a compound represented by Formula (1) wherein R 2 represents a 2-pyrimidinyl group;
a compound represented by Formula (1) wherein R 2 represents a 2-thienyl group;
a compound represented by Formula (1) wherein R 2 represents an acetyl group;
a compound represented by Formula (1) wherein R 2 represents a trifluoroacetyl group;
a compound represented by Formula (1) wherein R 2 represents an amino group;
a compound represented by Formula (1) wherein R 2 represents an acetylamino group;
a compound represented by Formula (1) wherein R 2 represents a trifluoroacetylamino group;
a compound represented by Formula (1) wherein R 2 represents a benzoylamino group;
a compound represented by Formula (1) wherein R 2 represents a 2-thienylcarbonylamino group;
a compound represented by Formula (1) wherein R 2 represents a 3-(2-chlorophenyl)ureido group;
a compound represented by Formula (1) wherein R 2 represents a methylsulfonylamino group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethylsulfonylamino group;
a compound represented by Formula (1) wherein R 2 represents a 4-methylphenylsulfonylamino group;
a compound represented by Formula (1) wherein R 2 represents a 4-chlorophenylsulfonylamino group;
a compound represented by Formula (1) wherein R 2 represents a benzylsulfonylamino group;
a compound represented by Formula (1) wherein R 2 represents a hydroxy group;
a compound represented by Formula (1) wherein R 2 represents a methoxy group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethoxy group;
a compound represented by Formula (1) wherein R 2 represents a methylthio group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethylthio group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethylsulfinyl group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethylsulfonyl group;
a compound represented by Formula (1) wherein R 3 represents a vinyl group;
a compound represented by Formula (1) wherein R 3 represents an ethynyl group;
a compound represented by Formula (1) wherein R 3 represents a 4-trifluoromethoxyphenyl group;
a compound represented by Formula (1) wherein R 3 represents a 6-trifluoromethyl-3-pyridyl group;
a compound represented by Formula (1) wherein R 3 represents a 1-difluoromethyl-3-pyrazolidyl group;
a compound represented by Formula (1) wherein R 3 represents an amino group;
a compound represented by Formula (1) wherein R 3 represents a hydroxy group;
a compound represented by Formula (1) wherein R 3 represents a methoxy group;
a compound represented by Formula (1) wherein R 3 represents a propargyloxy group;
a compound represented by Formula (1) wherein R 3 represents a 3-methoxybenzyloxy group;
a compound represented by Formula (1) wherein R 3 represents a 4-trifluoromethylbenzyloxy group;
a compound represented by Formula (1) wherein R 4 represents a 3-methylphenyl group;
a compound represented by Formula (1) wherein R 4 represents a 2-methoxyphenyl group;
a compound represented by Formula (1) wherein R 4 represents a hydroxy group;
a compound represented by Formula (1) wherein R 4 represents a methoxy group;
a compound represented by Formula (1) wherein R 4 represents a 2-methylphenoxy group;
a compound represented by Formula (1) wherein R 4 represents a 4-trifluoromethylphenoxy group;
a compound represented by Formula (1) wherein R 4 represents a 4-trifluoromethoxyphenoxy group;
a compound represented by Formula (1) wherein R 5 represents a 1-pyrrolyl group;
a compound represented by Formula (1) wherein R 5 represents an amino group;
a compound represented by Formula (1) wherein R 5 represents a methylamino group;
a compound represented by Formula (1) wherein R 5 represents a dimethylamino group;
a compound represented by Formula (1) wherein R 5 represents a formylamino group;
a compound represented by Formula (1) wherein R 5 represents an acetylamino group;
a compound represented by Formula (1) wherein R 5 represents a trifluoroacetylamino group;
a compound represented by Formula (1) wherein R 5 represents a benzoylamino group;
a compound represented by Formula (1) wherein R 5 represents a 5-bromo-2-thienylcarbonylamino group;
a compound represented by Formula (1) wherein R 5 represents a 2,5-dichloro-3-thienylcarbonylamino group;
›MODE FOR CARRYING OUT THE INVENTION · 28 of 73
a compound represented by Formula (1) wherein R 3 represents a 1-methyl-3-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 5 represents a 1,5-dimethyl-5-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 5 represents a 1,4-dimethyl-5-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 5 represents a 3-methyl-5-isoxazolylcarbonylamino group compound represented by Formula (1) wherein R 5 represents a hydroxy group;
a compound represented by Formula (1) wherein R 5 represents a methoxy group;
a compound represented by Formula (1) wherein R 5 represents an ethoxy group;
a compound represented by Formula (1) wherein R 5 represents an isopropoxy group;
a compound represented by Formula (1) wherein R 5 represents an allyloxy group;
a compound represented by Formula (1) wherein R 5 represents a benzyloxy group;
a compound represented by Formula (1) wherein R 5 represents an acetyloxy group;
a compound represented by Formula (1) wherein R 5 represents a 2-chlorobenzoyloxy group;
a compound represented by Formula (1) wherein R 5 represents a 4-methylphenylsulfonyloxy group;
a compound represented by Formula (1) wherein R 5 represents an N-methyl-aminosulfonyl group;
a compound represented by Formula (1) wherein R 5 represents an N-(3-chlorobenzyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 5 represents an N-(4-methylphenyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 5 represents an N-(4-methylphenyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 5 represents an N-(2-pyridylmethyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a fluorine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a chlorine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a bromine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents an iodine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a nitro group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents an amino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a dimethylamino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a methoxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a methyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a difluoromethyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a pentafluoroethyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a methoxycarbonyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a phenyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a 2-thienyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a chlorine atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a nitro group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents an amino group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a formylamino group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents an acetylamino group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a trifluoroacetylamino group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a benzoylamino group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a 5-bromo-2-thienylcarbonylamino group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a 2,5-dichloro-3-thienylcarbonylamino group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a 1-methyl-3-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a 1,5-dimethyl-3-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a 1,4-dimethyl-5-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a 3-methyl-5-isoxazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a hydroxy group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a methoxy group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents an ethoxy group;
a compound represented by Formula (1) wherein R-represents a hydrogen atom, and R 5 represents an isopropoxy group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents an allyloxy group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a benzyloxy group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents an acetyloxy group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a 2-chlorobenzoyloxy group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a 4-methylphenylsulfonyloxy group;
›MODE FOR CARRYING OUT THE INVENTION · 29 of 73
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents an N-methyl-aminosulfonyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 3 represents an N-(3-chlorobenzyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents an N-(4-methylphenyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents an N-(4-methylbenzyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents an N-(2-pyridylmethyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents an acetyloxy group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a methyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a heptafluoropropyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a methoxycarbonyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a prenyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a 1-pyrrolyl group;
a compound represented by Formula (1) wherein R-represents a chlorine atom, and R 5 represents an amino group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a cyano group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a nitro group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a fluorine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a chlorine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a bromine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents an iodine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a methyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a difluoromethyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a pentafluoroethyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a heptafluoropropyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a tert-butyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 2-chlorophenyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 3-chlorophenyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 4-chlorophenyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 4-trifluoromethylphenyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 2-pyridyl group, and R 3 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 3-pyridyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 4-pyridyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 2-pyrimidinyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 2-thienyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents an acetyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a trifluoroacetyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a benzoyl group, and R 3 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a methoxycarbonyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents an amino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents an acetylamino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a chloroacetylamino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a trifluoroacetylamino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a benzoylamino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 2-thienylcarbonylamino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a methylsulfonylamino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethylsulfonylamino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 4-chlorophenylsulfonylamino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a 4-methylphenylsulfonylamino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a benzylsulfonylamino group, and R 5 represents a hydrogen atom;
›MODE FOR CARRYING OUT THE INVENTION · 30 of 73
a compound represented by Formula (1) wherein R 2 represents a hydroxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a methoxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethoxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a methylthio group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethylthio group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethylsulfinyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethylsulfonyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a chlorine atom;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a nitro group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a methyl group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a methoxycarbonyl group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a phenyl group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a 1-pyrrolyl group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents an amino group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a formylamino group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents an acetylamino group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a trifluoroacetylamino group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a benzoylamino group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a 5-bromo-2-thienylcarbonylamino group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a 2,5-dichloro-3-thienylcarbonylamino group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a 1-methyl-3-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a 1,5-dimethyl-3-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a 1,4-dimethyl-5-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a 3-methyl-5-isoxazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents an N-methyl-aminosulfonyl group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents an N-(3-chlorobenzyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents an N-(4-methylphenyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents an N-(4-methylbenzyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents an N-(2-pyridylmethyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a hydroxy group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a methoxy group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents an ethoxy group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents an isopropoxy group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a benzyloxy group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents an acetyloxy group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a 2-chlorobenzoyloxy group;
a compound represented by Formula (1) wherein R 2 represents a hydrogen atom, and R 5 represents a 4-methylphenylsulfonyloxy group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a chlorine atom;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a methyl group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents an amino group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a methylamino group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a dimethylamino group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a formylamino group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents an acetylamino group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a trifluoroacetylamino group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a hydroxy group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents an ethoxy group;
›MODE FOR CARRYING OUT THE INVENTION · 31 of 73
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a methoxy group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents an isopropoxy group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents an allyloxy group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents a benzyloxy group;
a compound represented by Formula (1) wherein R 2 represents a trifluoromethyl group, and R 5 represents an acetyloxy group;
a compound represented by Formula (1) wherein R 2 represents a nitro group, and R 5 represents a hydroxy group;
a compound represented by Formula (1) wherein R 2 represents a 3-(2-chlorophenyl)ureido group, and R 5 represents a methoxy group;
a compound represented by Formula (1) wherein R 3 represents a nitro group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a fluorine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a chlorine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a bromine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a methyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a vinyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents an ethynyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a methoxycarbonyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a phenyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a 4-trifluoromethoxyphenyl group, and R represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a 6-trifluoromethyl-3-pyridyl group, and R represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents an amino group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a hydroxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a methoxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a propargyloxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a 3-methoxybenzyloxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a 4-trifluoromethylbenzyloxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents an acetyloxy group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R; represents a 2-chlorobenzoyloxy group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a 4-methylphenylsulfonyloxy group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a nitro group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a chlorine atom;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a methyl group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a heptafluoropropyl group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a methoxycarbonyl group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a phenyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, and R 5 represents a 1-pyrrolyl group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents an amino group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a methylamino group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a dimethylamino group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a formylamino group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents an acetylamino group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a trifluoroacetylamino group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a benzoylamino group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a hydroxy group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a methoxy group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents an ethoxy group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents an isopropoxy group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents an allyloxy group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a benzyloxy group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a 5-bromo-2-thienylcarbonylamino group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a 2,5-dichloro-3-thienylcarbonylamino group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a 1-methyl-3-pyrazolylcarbonylamino group;
›MODE FOR CARRYING OUT THE INVENTION · 32 of 73
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a 1,5-dimethyl-3-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a 1,4-dimethyl-5-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents a 3-methyl-5-isoxazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents an N-methyl-aminosulfonyl group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents an N-(3-chlorobenzyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents an N-(4-methylphenyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents an N-(4-methylbenzyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 3 represents a hydrogen atom, and R 5 represents an N-(2-pyridylmethyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 3 represents a 1-difluoromethyl-3-pyrazolyl group, and R 5 represents a chlorine atom;
a compound represented by Formula (1) wherein R 3 represents a trifluoromethyl group, and R 5 represents an amino group;
a compound represented by Formula (1) wherein R 4 represents a fluorine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a chlorine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a bromine atom, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a methyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a phenyl group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a hydroxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a methoxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a 2-methylphenoxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a 4-trifluoromethylphenoxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a nitro group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a chlorine atom;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a methyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a heptafluoropropyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a methoxycarbonyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a phenyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a 1-pyrrolyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents an amino group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a methylamino group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a dimethylamino group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a formylamino group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents an acetylamino group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a trifluoroacetylamino group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a benzoylamino group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a hydroxy group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a methoxy group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents an ethoxy group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents an isopropoxy group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents an allyloxy group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a benzyloxy group;
a compound represented by Formula (1) wherein R 4 represents a 4-trifluoromethoxyphenoxy group, and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents an acetyloxy group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a 2-chlorobenzoyloxy group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a 4-methylphenylsulfonyloxy group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a 5-bromo-2-thienylcarbonylamino group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a 2,5-dichloro-3-thienylcarbonylamino group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a 1-methyl-3-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a 1,5-dimethyl-3-pyrazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a 1,4-dimethyl-5-pyrazolylcarbonylamino group;
›MODE FOR CARRYING OUT THE INVENTION · 33 of 73
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents a 3-methyl-5-isoxazolylcarbonylamino group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents an N-methyl-aminosulfonyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents an N-(3-chlorobenzyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents an N-(4-methylphenyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents an N-(4-methylbenzyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 4 represents a hydrogen atom, and R 5 represents an N-(2-pyridylmethyl)-aminosulfonyl group;
a compound represented by Formula (1) wherein R 3 and R 4 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 and R 4 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 and R 3 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 and R 4 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 and R 2 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 and R 3 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 , R 3 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 , R 3 , and R 4 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 1 represents a methyl group;
a compound represented by Formula (1) wherein R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 1 represents a difluoromethyl group;
a compound represented by Formula (1) wherein R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 1 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 , R 3 , and R 1 each represents a hydrogen atom, and R 1 represents a pentafluoroethyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 1 represents a methyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 1 represents a difluoromethyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 1 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a pentafluoroethyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a methyl group;
a compound represented by Formula (1) wherein R 1 , R, and R 4 each represents a hydrogen atom, and R 2 represents a difluoromethyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a pentafluoroethyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a heptafluoropropyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a tert-butyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a methyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a difluoromethyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a pentafluoroethyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a heptafluoropropyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a tert-butyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a trifluoromethyl group;
›MODE FOR CARRYING OUT THE INVENTION · 34 of 73
a compound represented by Formula (1) wherein R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 1 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 1 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 1 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 1 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 1 represents a phenyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 1 represents a phenyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a phenyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a 2-chlorophenyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a 3-chlorophenyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a 4-chlorophenyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and R 2 represents a 4-trifluoromethylphenyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a phenyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a 2-chlorophenyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a 3-chlorophenyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a 4-chlorophenyl group;
a compound represented by Formula (1) wherein R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a 4-trifluoromethylphenyl group;
a compound represented by Formula (1) wherein R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 1 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, and R 3 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, and R 4 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 5 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 1 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, and R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, and R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein W represents —OR 6 ;
a compound represented by Formula (1) wherein W represents —OR 6 , —ON═CR 7 R 8 , or —SR 9 ;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 ;
a compound represented by Formula (1) wherein W represents —ON═CR 7 R 8 ;
a compound represented by Formula (1) wherein W represents —SR 9 ;
a compound represented by Formula (1) wherein W represents —OR 6 or —SR 9 ;
a compound represented by Formula (1) wherein W represents —OR 6 or —ON═CR 7 R 8 ;
a compound represented by Formula (1) wherein W represents —OR 6 or —NR 7 R 10 ;
a compound represented by Formula (1) wherein W represents —SR 9 or —NR 7 R 10 ;
›MODE FOR CARRYING OUT THE INVENTION · 35 of 73
a compound represented by Formula (1) wherein R 6 and R 9 each represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z, a C3-C6 alkynyl group optionally having one or more groups selected from the group X, a C7-C9 phenylalkyl group optionally having one or more groups selected from the group X, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 6 and R 9 each represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 6 and R 9 each represents a C1-C6 alkyl group;
a compound represented by Formula (1) wherein W represents —OR 6 or —SR 9 , and R 6 and R 9 each represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z, a C3-C6 alkynyl group optionally having one or more groups selected from the group X, a C7-C9 phenylalkyl group optionally having one or more groups selected from the group Y, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein W represents —OR 6 or —SR 9 , and R 6 and R 9 each represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein W represents —OR 6 or —SR 9 , and R 6 and R 9 each represents a C1-C6 alkyl group;
a compound represented by Formula (1) wherein W represents —OR 6 , and R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z, a C3-C6 alkynyl group optionally having one or more groups selected from the group X, a C7-C9 phenylalkyl group optionally having one or more groups selected from the group Y, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein W represents —OR 6 , and R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein W represents —OR 6 , and R 6 represents C1-C6 alkyl group;
a compound represented by Formula (1) wherein W represents —SR 9 , and R 9 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein W represents —SR 9 , and R 9 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein W represents —SR 9 , and R 9 represents a C1-C6 alkyl group;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 , and R 7 represents a hydrogen atom;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 , R 7 represents a hydrogen atom, and R 10 represents a hydrogen atom, a cyano group, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, a phenyl group optionally having one or more groups selected from the group Y, a benzyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y, —OH, or —NH 2 ;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 , R 7 represents a hydrogen atom, and R 10 represents a hydrogen atom, a cyano group, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, a phenyl group optionally having one or more groups selected from the group Y, —OH, or —NH 2 ;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 , R 7 represents a hydrogen atom, and R 10 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 , R 7 represents a hydrogen atom, and R 10 represents a hydrogen atom or a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 , R 7 represents a hydrogen atom, and R 10 represents a hydrogen atom or a C1-C6 alkyl group;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 , and R 10 represents a hydrogen atom, a cyano group, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, a phenyl group optionally having one or more groups selected from the group Y, —OH, or —NH 2 ;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 , and R 10 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 , and R 10 represents a hydrogen atom or a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 , and R 10 represents a hydrogen atom or a C1-C6 alkyl group;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 , and R 10 represents a cyano group, —OH, or —NH 2 ;
a compound represented by Formula (1) wherein W represents —NR 7 R 10 , R 7 represents a hydrogen atom, and R 10 represents a cyano group, —OH, or —NH 2 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
›MODE FOR CARRYING OUT THE INVENTION · 36 of 73
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and
R 5 represents a halogen atom, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 14 , a phenyl group optionally having one or more groups selected from the group Y, or a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y,
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y,
R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms,
R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and
R 14 represents a C1-C4 alkyl group optionally having one or more groups selected from the group X or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a halogen atom, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , or —S(O) 2 NR 7 R 11 , —OR 14 , a phenyl group optionally having one or more groups selected from the group Y, or a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and
W represents —OR 6 or —SR 9 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
›MODE FOR CARRYING OUT THE INVENTION · 37 of 73
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y,
W represents —OR 6 or —SR 9 , and
R 6 and R 9 each represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a CL-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y,
W represents —OR 6 or —SR 9 , and
R 6 and R 9 each represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y,
W represents —OR 6 or —SR 9 , and
R 6 and R 9 represent a C1-C6 alkyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a halogen atom, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 14 , a phenyl group optionally having one or more groups selected from the group Y, or a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y,
W represents —OR 6 , and
R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
›MODE FOR CARRYING OUT THE INVENTION · 38 of 73
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a halogen atom, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 14 , a phenyl group optionally having one or more groups selected from the group Y, or a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y,
W represents —OR 6 , and
R 6 represents a C1-C6 alkyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y, and
W represents —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m 11 ,
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y,
W represents —NR 7 R 10 , and R 7 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y,
W represents —NR 7 R 10 ,
R 7 represents a hydrogen atom, and
R 10 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
›MODE FOR CARRYING OUT THE INVENTION · 39 of 73
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y,
W represents —NR 7 R 10 ,
R 7 represents a hydrogen atom, and
R 10 represents a hydrogen atom or a C1-C6 alkyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 5 represents a halogen atom, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 14 , a phenyl group optionally having one or more groups selected from the group Y, or a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y,
W represents —OR 6 , and
R 6 represents a C1-C6 alkyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y,
W represents —NR 7 R 10 ,
R 7 represents a hydrogen atom; and
R 10 represents a hydrogen atom or a C1-C6 alkyl group;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and
R 2 , R 3 , and R 4 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, and
R 2 represents a halogen atom, a cyano group, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, an amino carbonyl group, —NR 12 R 13 , —OR 13 , —S(O) m R 13 , or —SF 5 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 represent a hydrogen atom, and
R 3 represents a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, C2-C6 alkenyl group optionally having one or more groups selected from the group X, a C2-C6 alkynyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ;
›MODE FOR CARRYING OUT THE INVENTION · 40 of 73
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, and
R 4 represents a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and
R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, and
R 2 represents a halogen atom, a cyano group, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, an aminocarbonyl group, —NR 12 R 13 , —OR 13 , —S(O) m R 13 , or —SF 5 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, and
R 3 represents a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a C2-C6 alkenyl group optionally having one or more groups selected from the group X, a C2-C6 alkynyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, and
R 4 represents a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom, and
R 5 represents a halogen atom, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 14 , a phenyl group optionally having one or more groups selected from the group Y, or a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom, and
R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom,
R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and
R 14 represents a C1-C4 alkyl group optionally having one or more groups selected from the group X, a C7-C9 phenylalkyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y, a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, a benzoyl group optionally having one or more groups selected from the group Y, a phenylsulfonyl group optionally having one or more groups selected from the group Y, or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom,
R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and
R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom, and
R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom,
R 5 represents —OR 14 , and
R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and
›MODE FOR CARRYING OUT THE INVENTION · 41 of 73
R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 12 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents —OR 14 , and
R 14 represents a C1-C4 alkyl group optionally having one or more groups selected from the group X or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and
R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and
R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and
R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 5 represents —OR 14 , and
›MODE FOR CARRYING OUT THE INVENTION · 42 of 73
R 14 represents a C1-C4 alkyl group optionally having one or more groups selected from the group X or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 or —S(O) m R 11 ,
R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms,
R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and
R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 5 represents a hydrogen atom,
R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and
R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and
R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a trifluoromethyl group,
W represents —OR 6 , and
R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
›MODE FOR CARRYING OUT THE INVENTION · 43 of 73
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a trifluoromethyl group, and W represents —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a trifluoromethyl group,
W represents —NR 7 R 10 ,
R 7 represents a hydrogen atom, and
R 10 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 5 represents a trifluoromethyl group, and
W represents —SR 9 ,
R 9 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 11 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and
R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 5 represents a trifluoromethyl group,
R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and
R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
›MODE FOR CARRYING OUT THE INVENTION · 44 of 73
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 5 represents a trifluoromethyl group,
R 11 represents a methyl group or a trifluoromethyl group, and
R 13 represents a methyl group or a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 5 represents a hydrogen atom,
R 11 represents a methyl group or a trifluoromethyl group, and
R 13 represents a methyl group or a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 5 represents a trifluoromethyl group,
R 11 represents a methyl group, and
R 13 represents a methyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ,
R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 5 represents a hydrogen atom,
R 11 represents a methyl group, and
R 13 represents a methyl group;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 ,
R 2 , R 3 , and R 4 each represents a hydrogen atom, and
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom,
R 2 represents a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , and
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom,
R 3 represents a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 represent a hydrogen atom,
R 4 represents a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and
R 5 represents a halogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y;
›MODE FOR CARRYING OUT THE INVENTION · 45 of 73
a compound represented by Formula (1) wherein R 1 represents a halogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and
R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and
R 2 represents a halogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, and
R 3 represents a halogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, and
R 4 represents a halogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 ,
R 2 , R 3 , and R 4 each represents a hydrogen atom, and
R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom,
R 2 represents a halogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , and
R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom,
R 3 represents a halogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and
R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom,
R 4 represents a halogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and
R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, and R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R each represents a hydrogen atom, and R 2 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, and R 3 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, and R 4 represents a halogen atom;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and
R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, and
R 3 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, and
R 4 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X;
a compound represented by Formula (1) wherein R 1 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and
R represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, and
R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, and
R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, and R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group,
R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom,
W represents a —OR 6 , and
R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group,
R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom,
W represents a —OR 6 , and
R 6 represents a C3-C6 alkyl group;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group,
R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and W represents —ON═CR 7 R 8 , —SR 9 , or —NR 7 R 10 ;
›MODE FOR CARRYING OUT THE INVENTION · 46 of 73
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group,
R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and W represents —ON═CR 7 R 8 ;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group,
R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and W represents —SR 9 ;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group,
R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom,
W represents —SR 9 , and
R 9 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group,
R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and W represents —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group,
R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom,
W represents —NR 7 R 10 , R 1 represents a hydrogen atom, and R 10 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, R 2 represents a trifluoromethyl group, W represents —OR 6 , and R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, R 2 represents a trifluoromethyl group, W represents —OR 6 , and R 6 represents a C3-C6 alkyl group;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, R represents a trifluoromethyl group, and W represents —ON═CR 7 R 8 , —SR 9 , or —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, R 2 represents a trifluoromethyl group, and W represents —ON═CR 7 R 8 ;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, R 2 represents a trifluoromethyl group, and W represents —SR 9 ;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, R 2 represents a trifluoromethyl group, W represents —SR 9 , and R 9 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, R 2 represents a trifluoromethyl group, and W represents —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, R 2 represents a trifluoromethyl group, W represents —NR 7 R 10 , R 7 represents a hydrogen atom, and R 10 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, and R 3 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, R 3 represents a trifluoromethyl group, W represents —OR 6 , and R 6 represents a CL-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, R 3 represents a trifluoromethyl group, W represents —OR 6 , and R 6 represents a C3-C6 alkyl group;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, R 3 represents a trifluoromethyl group, and W represents —ON═CR 7 R 8 , —SR 9 , or —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, R 3 represents a trifluoromethyl group, and W represents —ON═CR 7 R 8 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, R 3 represents a trifluoromethyl group, and W represents —SR 9 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, R 3 represents a trifluoromethyl group, W represents —SR 9 , and R 9 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, R 3 represents a trifluoromethyl group, and W represents —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 1 , and R 5 each represents a hydrogen atom, R 3 represents a trifluoromethyl group, W represents —NR 7 R 10 , R 7 represents a hydrogen atom, and R 10 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, and R 4 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, R 4 represents a trifluoromethyl group, W represents —OR 6 , and R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, R 4 represents a trifluoromethyl group, W represents —OR 6 , and R 6 represents a C3-C6 alkyl group;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, R 4 represents a trifluoromethyl group, and W represents —ON═CR 7 R 8 , —SR 9 , or —NR 7 R 10 ;
›MODE FOR CARRYING OUT THE INVENTION · 47 of 73
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, R 4 represents a trifluoromethyl group, and W represents —ON═CR 7 R 8 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, R 4 represents a trifluoromethyl group, and W represents —SR 9 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, R 4 represents a trifluoromethyl group, W represents —SR 9 , and R 9 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, R 4 represents a trifluoromethyl group, and W represents —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, R 4 represents a trifluoromethyl group, W represents —NR 7 R 10 , R 7 represents a hydrogen atom, and R 10 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 represent a hydrogen atom, and R 5 represents a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a trifluoromethyl group, W represents —OR 6 , and R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a trifluoromethyl group, and W represents —ON═CR 7 R 8 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a trifluoromethyl group, and W represents —SR 9 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a trifluoromethyl group, W represents —SR 9 , and R 9 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a trifluoromethyl group, and W represents —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a trifluoromethyl group, W represents —NR 7 R 10 , and R 7 represents a hydrogen atom, and R 10 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y, and R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, and R 3 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R each represents a hydrogen atom, and R 4 represents a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents —OR 11 , and R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents —OR 13 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, and R 3 represents —OR 11 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, and R 4 represents —OR 11 ;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 6 , and R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 2 represents or —S(O) m R 13 ;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, and R 3 represents or —S(O) m R 11 ,
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, and R 4 represents or —S(O) m R 11 ;
a compound represented by Formula (1) wherein R 1 represents —OR 10 , R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, R 2 represents —OR 13 , and R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, R 3 represents —OR 11 , and R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, R 4 represents —OR 11 , and R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 11 , R 2 , R 3 , R 4 , and R 5 each represents a hydrogen atom, and R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 3 , R 4 , and R 5 each represents a hydrogen atom, R 2 represents —S(O) m R 13 , and R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 2 , R 4 , and R 5 each represents a hydrogen atom, R 3 represents —S(O) m R 11 , and R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
›MODE FOR CARRYING OUT THE INVENTION · 48 of 73
a compound represented by Formula (1) wherein R 1 , R 2 , R 3 , and R 5 each represents a hydrogen atom, R 4 represents —S(O) m R 11 , and R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents a halogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents a halogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 4 represents a halogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 4 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a C1-C4 alkyl group optionally having one or more halogen atoms, R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 1 represents a halogen atom, a cyano group, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C5 alkoxycarbonyl group, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents a trifluoromethyl group, and R 5 represents a halogen atom, a cyano group, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C5 alkoxycarbonyl group, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents a trifluoromethyl group, and R 5 represents a halogen atom, a cyano group, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C5 alkoxycarbonyl group, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 , R, and R 3 each represents a hydrogen atom, R 4 represents a trifluoromethyl group, and R 5 represents a halogen atom, a cyano group, a nitro group, a C1-C4 alkyl group optionally having one or more halogen atoms, a C2-C5 alkoxycarbonyl group, —NR 11 R 12 , —S(O) 2 NR 7 R 11 , —OR 14 , or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents a trifluoromethyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents a trifluoromethyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 4 represents a trifluoromethyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
›MODE FOR CARRYING OUT THE INVENTION · 49 of 73
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more groups selected from the group X or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents a trifluoromethyl group, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one cr more groups selected from the group X or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents a trifluoromethyl group, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more groups selected from the group X or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 4 represents a trifluoromethyl group, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more groups selected from the group X or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a trifluoromethyl group, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents a trifluoromethyl group, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents a trifluoromethyl group, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 4 represents a trifluoromethyl group, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y, R 2 , R 3 , and R 4 each represents a hydrogen atom, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 4 represents a phenyl group optionally having one or more groups selected from the group Y, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 1 R 12 , or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents —OR 11 , R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 , and R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents —OR 13 , R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 , and R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents —OR 11 , R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 , and R 11 , represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 4 represents —OR 11 , R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 , and R 1 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 11 , R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 , and R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents —S(O) m R 13 , R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 , and R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents —S(O) m R 11 , R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 , and R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
›MODE FOR CARRYING OUT THE INVENTION · 50 of 73
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 1 represents —S(O) m R 11 , R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms, —NR 11 R 12 , or —OR 14 , and R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a halogen atom, R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents a halogen atom, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents a halogen atom, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 4 represents a halogen atom, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (l) wherein R 1 represents a phenyl group optionally having one or more groups selected from the group Y, R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents a phenyl group optionally having one or more groups selected from the group Y, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents a phenyl group optionally having one or more groups selected from the group Y, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 4 represents a phenyl group optionally having one or more groups selected from the group Y, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R-represents —OR 11 , R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents —OR 13 , R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents —OR, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 4 represents —OR 11 , R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents —S(O) m R 11 , R 2 , R 3 , and R 4 each represents a hydrogen atom, R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 3 , and R 4 each represents a hydrogen atom, R 2 represents —S(O) m R 13 , R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 4 each represents a hydrogen atom, R 3 represents —S(O) m R 11 , R 3 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 , R 2 , and R 3 each represents a hydrogen atom, R 4 represents —S(O) m R 11 , R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
›MODE FOR CARRYING OUT THE INVENTION · 51 of 73
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and R 1 represents a hydrogen atom, a C1-C4 alkyl group, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a C1-C4 alkyl group, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , W represents —OR 6 , and R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and R 1 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , and W represents —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and R 1 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , W represents —NR 7 R 10 , R 7 represents a hydrogen atom, and R 10 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z or a phenyl group optionally having one or more groups selected from the group Y;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 11 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and R 1 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , W represents —SR 9 , and R 9 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
›MODE FOR CARRYING OUT THE INVENTION · 52 of 73
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and R 1 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group or a trifluoromethyl group, R 13 represents a methyl group or a trifluoromethyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group, R 13 represents a methyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and R 5 represents a hydrogen atom;
›MODE FOR CARRYING OUT THE INVENTION · 53 of 73
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, R 11 represents a methyl group or a trifluoromethyl group, and R 13 represents a methyl group or a trifluoromethyl group;
a compound represented by Formula (1) wherein R-represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, R 1 represents a methyl group, and R 13 represents a methyl group;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 11 represents C1-C3 alkyl group optionally having one or more halogen atoms, R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
›MODE FOR CARRYING OUT THE INVENTION · 54 of 73
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group which may have optionally one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group or a trifluoromethyl group, R 13 represents a methyl group or a trifluoromethyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a trifluoromethyl group, R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group, R 13 represents a methyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and R 1 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , W represents —OR 6 , and R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , and W represents —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , W represents —NR 7 R 10 , R 7 represents a hydrogen atom, and R 10 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
›MODE FOR CARRYING OUT THE INVENTION · 55 of 73
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a C1-C4 alkyl group which may have optionally one or more halogen atoms, or —OR 14 , W represents —SR 9 , and R 3 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 7 , or —S(O) m R 11 , and R 1 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group or a trifluoromethyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and R 5 represents a hydrogen atom;
›MODE FOR CARRYING OUT THE INVENTION · 56 of 73
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, and R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, and R 11 represents a methyl group or a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, and R 1 represents a methyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms;
›MODE FOR CARRYING OUT THE INVENTION · 57 of 73
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 or —S(O) m R 11 , R 5 represents a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group or a trifluoromethyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a C1-C4 alkyl group which may have optionally one or more halogen atoms, or —OR 14 , W represents —OR 6 , and R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 2 R 11 , —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , and W represents —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , W represents —NR 7 R 10 , R 7 represents a hydrogen atom, and R 10 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
›MODE FOR CARRYING OUT THE INVENTION · 58 of 73
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , W represents a —SR 9 , and R 9 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and R 1 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 9 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , R 6 represents a C1-C3 alkyl group optionally having one or more halogen atoms, R 9 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group or a trifluoromethyl group, R 13 represents a methyl group or a trifluoromethyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group, R 13 represents a methyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and R 5 represents a hydrogen atom;
›MODE FOR CARRYING OUT THE INVENTION · 59 of 73
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and R 5 represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, R 1 represents a methyl group or a trifluoromethyl group, and R 13 represents a methyl group or a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a hydrogen atom, R 11 represents a methyl group, and R 13 represents a methyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
›MODE FOR CARRYING OUT THE INVENTION · 60 of 73
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group or a trifluoromethyl group, R 13 represents a methyl group or a trifluoromethyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, methyl group, a trifluoromethyl group, a phenyl group which may have optionally one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a trifluoromethyl group, R 4 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 5 represents a methyl group, a trifluoromethyl group, or —OR 14 , R represents a methyl group, R 13 represents a methyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, and R 1 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , W represents —OR 6 , and R 6 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , and W represents —NR 7 R 10 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 13 , —OR 11 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 7 represents a hydrogen atom, and R 13 represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group Z, or a phenyl group optionally having one or more groups selected from the group Y;
›MODE FOR CARRYING OUT THE INVENTION · 61 of 73
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , W represents —SR 9 , and R 9 represents a C1-C6 alkyl group optionally having one or more groups selected from the group Z;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group which may have optionally one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, and R 1 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, R 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more halogen atoms, or —OR 14 , R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 4 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, R 3 represents a hydrogen atom, a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group or a trifluoromethyl group, R 13 represents a methyl group or a trifluoromethyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, R 5 represents a hydrogen atom, a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group, R 13 represents a methyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, and R 5 represents a hydrogen atom;
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a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, and R=represents a hydrogen atom;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, R 5 represents a hydrogen atom, R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, R 5 represents a hydrogen atom, R 11 represents a methyl group or a trifluoromethyl group, and R 13 represents a methyl group or a trifluoromethyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 1 represents a trifluoromethyl group, R 5 represents a hydrogen atom, R 11 represents a methyl group, and R 13 represents a methyl group;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 12 R 13 , —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —NR 11 R 12 , —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 11 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 11 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 7 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, and R 5 represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 ;
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a C1-C6 alkyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, R represents a C1-C4 alkyl group optionally having one or more halogen atoms or —OR 14 , R 11 represents a C1-C3 alkyl group optionally having one or more halogen atoms, R 13 represents a C1-C3 alkyl group optionally having one or more halogen atoms, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms, or a hydrogen atom;
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a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 , represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, R 5 represents a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group or a trifluoromethyl group, R 13 represents a methyl group or a trifluoromethyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom
a compound represented by Formula (1) wherein R 1 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 2 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 13 , or —S(O) m R 13 , R 3 represents a hydrogen atom, a halogen atom, a nitro group, a methyl group, a trifluoromethyl group, a phenyl group optionally having one or more groups selected from the group Y, —OR 11 , or —S(O) m R 11 , R 4 represents a trifluoromethyl group, R 5 represents a methyl group, a trifluoromethyl group, or —OR 14 , R 11 represents a methyl group, R 13 represents a methyl group, and R 14 represents a C1-C4 alkyl group optionally having one or more halogen atoms or a hydrogen atom.
When the compound of the present invention is used in the method of the present invention, the compound of the present invention may be used alone. However, as described below, the compound may be used as a composition for promoting plant growth that is formulated using various inactive ingredients (solid carriers, liquid carriers, surfactants, other adjuvant for formulation, and the like).
Examples of the solid carriers used for formulation include fine powdery or granular materials and the like that formed of minerals such as kaolin clay, attapulgite clay, bentonite, montmorillonite, Japanese acid clay, pyrophyllite, talc, diatomaceous earth, and calcite, natural organic substances such as corn rachis powder and walnut shell powder, synthetic organic substances such as urea, salts such as calcium carbonate and ammonium sulfate, or synthetic inorganic substances such as synthetic hydrous silicon oxide. Examples of the liquid carriers include aromatic hydrocarbons such as xylene, alkylbenzene, and methylnaphthalene, alcohols such as 2-propanol, ethylene glycol, propylene glycol, and ethylene glycol monoethyl ether, ketones such as acetone, cyclohexanone, and isophorone, plant oil such as soybean oil and cotton seed oil, petroleum-based aliphatic hydrocarbons, esters, dimethylsulfoxide, acetonitrile, water, and the like.
Examples of the surfactants include anionic surfactants such as an alkyl sulfuric acid ester salt, an alkyl aryl sulfonic acid salt, a dialkyl sulfosuccinic acid salt, a polyoxyethylene alkyl aryl ether phosphoric acid ester salt, lignin sulfonic acid salt, and a naphthalene sulfonate formaldehyde polycondensate, nonionic surfactants such as polyoxyethylene alkyl aryl ether, a polyoxyethylene alkyl polyoxypropylene block copolymer, and a sorbitan aliphatic ester, and cationic surfactants such as an alkyl trimethyl ammonium salt.
Examples of other adjuvants for formulation include water-soluble polymers such as polyvinyl alcohol and polyvinyl pyrrolidone, gum Arabic, alginic acid and a salt thereof, polysaccharides such as carboxymethylcellulose (CMC) and xanthan gum, inorganic substances such as aluminum magnesium silicate and alumina sol, preservatives, colorants, and stabilizing agents such as isopropyl acid phosphate (PAP) and BHT.
In the method of the present invention, when a plant is treated with the compound of the present invention, the plant or the plantation thereof is treated with the compound of the present invention at an effective dose. When the plant or the plantation of the plant is treated, it is treated once or plural times with the compound of the present invention.
Specific examples of the application method of the present invention include treating of the foliage, flower organs, or ear of a plant by means of spraying the compound to the foliage, soil (plantation) treatment that is performed before or after a plant is planted, seed treatment such as seed sterilization, seed soaking, or seed coating, seedling treatment, treating of a bulb such as a seed tuber, and the like.
In the method of the present invention, examples of the treating of the foliage, flower organs, or ears of a plant include a treatment method by applying the compound onto the surface of a plant by means of spraying the compound to foliage, stem, and the like. The examples also include a method of performing spraying treatment on flower organs or the entire plant during the flowering period including a pre-flowering stage, a mid-flowering stage, and a post-flowering stage. Moreover, for grain and the like, the examples include a spraying method performed on the ears or the entire plant during the period of ear emergence.
Examples of the soil treatment method in the method of the present invention include spraying to soil, soil incorporation, and drenching soil with liquid chemical (liquid chemical irrigation, soil injection, or liquid chemical dripping). Examples of the place to be treated include planting holes, planting rows, the vicinity of planting holes, the vicinity of planting rows, the entire area of plantation, the vicinity of plantation, inter-row spaces, places under the stem, a ridge between main stems, culture soil, a seedling box, a seedling tray, a seedbed, and the like. The treatment is performed, for example, during a pre-seeding stage, a seeding stage, a stage immediately after seeding, and during the growing period including a seedling raising stage, a pre-planting stage, at a planting stage, and the post-planting stage. Further, in the soil treatment, a plant may be treated with plural kinds of compounds of the present invention at the same time, and a solid fertilizer such as a paste fertilizer containing the compound of the present invention may be applied to the soil. Moreover, the compound of the present invention may be mixed into a liquid for irrigation by means of, for example, by being injected into irrigation facilities (an irrigation tube, an irrigation pipe, a sprinkler, and the like), mixed into a liquid for inter-row space irrigation, or mixed into a hydroponic medium. In addition, the compound of the present invention may be mixed with the liquid for irrigation in advance to perform the treatment by means of, for example, the above irrigation method or other appropriate irrigation methods such as spraying of water and flooding.
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In the present invention, the plant seed treated with the compound of the present invention retains the compound of the present invention at an effective dose, in the inside or surface of the plant seed or in the coated portion formed in the circumference of the plant seed. In the method of the present invention, the treating of seeds is a method of treating seeds or bulbs of a plant as a target with the compound of the present invention. Specific examples thereof include spraying treatment in which a suspension of the compound of the present invention is sprayed onto the seed surface or the bulb surface in the form of mist, smearing treatment in which wettable powder, an emulsion, or a flowable agent of the compound of the present invention is used as is or used by being supplemented with a small amount of water so as to coat the seed or bulb, a soaking treatment in which the seeds are soaked into the solution of the present compound for a certain time, film coating treatment, pellet coating treatment, and the like. Moreover, in the present invention, the plant seeds treated with the compound of the present invention are seeds of a plant that have not yet been seeded to soil or a culture medium.
In the method of the present invention, examples of the seedling treatment include spraying treatment in which the compound of the present invention is prepared by being diluted with water to yield an appropriate concentration of active ingredients, and the diluted solution is sprayed to the entire seedling, soaking treatment in which the seedling is soaked into the diluted solution, coating treatment in which the compound of the present invention that is prepared as a dust formulation is applied to the entire seedling, and seedling-growing box treatment in which the culture soil that is being used to raise seedling is treated with the compound of the present invention at an effective dose. Moreover, examples of the soil treatment performed before or after seedlings are planted include a method in which a diluted solution, which is prepared by diluting the compound of the present invention with water to yield an appropriate concentration of active ingredients, is sprayed to the seedlings or the surrounding soil after the seedlings are planted, and a method in which the compound of the present invention that is prepared as granules or a solid formulation such as granules is sprayed to the surrounding soil after the seedlings are planted.
Further, the compound of the present invention may be used by being mixed with a hydroponic medium in hydroponic culture, or used as one of medium components in tissue culture. Regarding hydroponic treatment method in the method of the present invention, when the compound is used for hydroponic culture, the compound may be used by being dissolved or suspended in a hydroponic medium for hydroponic culture that is generally used for a horticultural experiment and the like, within a range of a concentration thereof in the medium of 0.001 ppm to 1,000 ppm. Moreover, when the compound is used for tissue culture or cell culture, the compound may be used by being dissolved or suspended in a generally used medium for plant tissue culture, such as Murashige & Scoog medium, or a hydroponic medium such as Hoagland hydroponic culture solution, within a range of a concentration thereof in the medium of 0.001 ppm to 1,000 ppm. In this case, saccharides as a carbon source, various plant hormones, and the like may be appropriately added according to the conventional method.
When the compound of the present invention is used to treat a plant or a place where the plant grows, the amount of the compound used for the treatment varies with the type of plant to be treated, the form of formulation, the time of treatment, weather conditions, and the like. However, the amount is generally within a range of 0.1 g to 10,000 g and preferably within a range of 1 g to 1,000 g, in terms of the amount of active ingredients per 10,000 m 2 . When the compound is mixed with the entire soil, the amount of the compound used for the treatment is generally 0.1 g to 10,000 g and preferably 1 g to 1,000 g, in terms of the amount of active ingredients per 10,000 m 2 .
The emulsion, wettable powder, flowable agent, microcapsules, and the like are used for the treatment generally by being diluted with water and sprayed. In this case, the concentration of active ingredients is generally within a range of 0.1 ppm to 10,000 ppm, and preferably within a range of 1 ppm to 1,000 ppm. Powder, granules, and the like are generally used as they are without being diluted.
During the seed treatment, a weight of the compound of the present invention per 100 Kg of seeds is generally within a range of 0.01 g to 1,000 g and preferably within a range of 0.1 g to 100 g.
Examples of plants to which the method of the present invention is applicable include the following.
Crops: corn, rice, wheat, barley, rye, oat, sorghum, cotton, soybean, peanut, buckwheat, sugar beet, colza, sunflower, sugar cane, tobacco, hop, and the like
Vegetables: vegetables from Solanaceae family (eggplant, tomato, potato, pepper, bell pepper, and the like), vegetables from Cucurbitaceous family (cucumber, squash, zucchini, watermelon, melon, oriental melon, and the like), vegetables from Cruciferous family (radish, turnip, horseradish, kohlrabi, napa cabbage, cabbage, rape, mustard, broccoli, cauliflower, and the like), vegetables from Compositae family (burdock, edible chrysanthemum, artichoke, lettuce, and the like), vegetables from Liliceae family (green onion, onion, garlic, asparagus, and the like), vegetables from Apiaceae family (carrot, parsley, celery, parsnip, and the like), vegetables from Chenopodiaceae family (spinach, chard, and the like), vegetables from Lamiaceae family (Japanese basil, mint, basil, and the like), crops from Laguminosae family (pea, common bean, azuki bean, broad bean, chickpea, and the like), strawberry, sweet potato, Japanese yam, taro, konjac, ginger, okra, and the like
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Fruit trees: pomaceous fruits (apple, pear, European pear, Chinese quince, quince, and the like), stone fruits (peach, plum, nectarine, Japanese apricot, cherry, apricot, prune, and the like), citrus (Citrus unshiu, orange, lemon, lime, grapefruit, and the like), nuts (chestnut, walnut, hazelnut, almond, pistachio, cashew nut, macadamia nut, and the like), berries (blueberry, cranberry, blackberry, raspberry, and the like), grape, persimmon, olive, loquat, banana, coffee, date, coconut, oil palm, and the like
Trees other than fruit trees: tea, a mulberry tree, flowering trees (chive, camellia, hydrangea, sasanqua, Japanese star anise, cherry, tulip tree, crape myrtle, fragrant olive, and the like), roadside trees (ash, birch, dogwood, eucalyptus, gingko, lilac, maple, oak, poplar, cercis, liquidambar, plane, Japanese zelkova, Japanese arborvitae, fir, southern Japanese hemlock, juniper, pine, spruce, yew, elm, buckeye, and the like), sweet viburnum, yew plum pine, Japanese cedar, Japanese cypress, croton, Japanese spindle tree, Japanese photinia, and the like
Lawn: grasses (zoysia grass, Zoysia Matrella, and the like), bermuda grasses (Cynodon Dactylon, and the like), bentgrasses (wood medowgrass, creeping bentgrass, colonial bent, and the like), bluegrasses (Kentucky bluegrass, Poa compressa, and the like), fescues (fescue grass, Festuca rubra , and the like), ryegrasses ( Lolium multiporum Lam, Lolium pererne , and the like), orchardgrass, timothy grass, and the like
Others: flowers and ornamental plants (rose, carnation, chrysanthemum, Russell prairie gentian, gypsophila, gerbera, marigold, salvia, petunia, verbena, tulip, aster, gentian, lily, pansy, cyclamen, orchid, lily of valley, lavender, stock, ornamental cabbage, primula, poinsettia, gladiolus, cattleya, daisy, cymbidium, begonia, and the like), biofuel plants (jatropha, safflower, camelinas, switchgrass, miscanthus, reed canarygrass, Arundo donax, Ambry hemp, cassava, withy, and the like), foliage plants, and the like
Examples of plants applicable to the present invention preferably include tea, apple, pear, grape, cherry, peach, nectarine, persimmon, Japanese apricot, plum, soybean, lettuce, cabbage, tomato, eggplant, cucumber, watermelon, melon, common bean, peas, azuki bean, grasses, colza, strawberry, almond, corn, sorghum, broad beans, napa, potato, peanut, rice, wheat, taro, konjac, Japanese yam, radish, turnip, parsley, oriental melon, okra, ginger, lemon, orange, grapefruit, lime, blueberry, chestnut, hop, basil, more preferably include plants from the Poaceae family or plants from the Solanaceae family, even more preferably include plants from the Poaceae family, and still more preferably include rice, wheat, corn, and the like.
The above “plant” may be a plant into which a gene which imparts herbicide resistance to a plant, a gene which selectively produces toxicity for harmful insects, a gene which imparts disease resistance to a plant, a gene which relieve abiotic stress, and the like have been introduced by gene recombination or cross-breeding, or may be a stacked GM plant composed of plural kinds of combinations of these.
The compound of the present invention may be used simultaneously with an insecticide, a fungicide, or a safener for a certain herbicide to treat seeds, or may be applied to the plant simultaneously with the above agents.
In the method of the present invention, the plant to be treated with the compound of the present invention may be a plant that has been or will be exposed to abiotic stress. The degree of the abiotic stress that is indicated by the value of “stress intensity” described in the following formula may be 105 to 200, preferably 110 to 180, and more preferably 120 to 160.
Formula (1): “stress intensity”=100דone of the plant phenotypes in a plant that has not yet been exposed to abiotic stress conditions”/“one of the plant phenotypes in the above plant that has been exposed to abiotic stress conditions”
The term “abiotic stress” as used herein means the stress that causes a decline in physiological functions of cells of a plant, when the plant is exposed to an abiotic stress condition, and then deterioration in the physiological state of the plant, leading to its growth inhibition, such as temperature stress, i.e. high-temperature stress or low-temperature stress, water stress, i.e. drought stress or excess water stress, and salt stress. The high-temperature stress refers to the stress that a plant suffers from when the plant is exposed to a temperature higher than the temperature appropriate for the growth or germination of the plant. Specifically, for example, this type of stress may be caused when an average cultivation temperature of the environment in which a plant is cultured is under condition of 25° C. or higher, more strictly 30° C. or higher, and even more strictly 35° C. or higher. The low-temperature stress refers to the stress that a plant suffers from when the plant is exposed to a temperature lower than the temperature appropriate for the growth or germination of the plant. Specifically, for example, this type of stress may be caused when an average cultivation temperature of the environment in which a plant is cultured is under condition of 15° C. or lower, more strictly 10° C. or lower, and even more strictly 5° C. or lower. Moreover, the drought stress refers to the stress that a plant suffers from when the water content in soil is reduced by the decrease in precipitation or watering amount, water absorption of the plant is hindered, and the plant is exposed to a water environment that may hinder the growth of the plant. Specifically, for example, this type of stress may be caused when a moisture content of soil in which the plant is cultured is under the condition of 15% by weight or less, more strictly 10% by weight or less, and even more strictly 7.5% by weight or less which may causes water stress, or a pF value of soil in which the plant is cultured is under the condition of 2.3 or higher, strictly 2.7 or higher, and even more strictly 3.0 or higher, though these values may vary with the type of soil. The excess water stress refers to the stress that a plant suffers from when the plant is exposed to a water environment in which a water content in the soil becomes excessive, and the growth of the plant may be hindered. The excess water stress refers to the stress that a plant suffers from when a water content in the soil becomes excessive, and the growth of the plant may be hindered. Specifically, for example, this type of stress may be caused when a moisture content of the soil in which the plant is cultured is under the condition of 30% by weight or more, more strictly 40% by weight or more, and even more strictly 50% by weight or more, or a pF value of the soil in which the plant is cultured is under the condition of 1.7 or less, strictly 1.0 or less, and even more strictly 0.3 or less, though these values may vary with the type of soil. Further, the pF value of soil may be measured according to the principle described in “Dictionary of Soil-Plant Nutrition•Environment” (TAIYOSHA, CO., LTD., 1994, Matsusaka et al.), pp 61-62, “pF value measurement method”. In addition, the salt stress refers to the stress that a plant suffers from when salts accumulate in the soil or hydroponic medium in which a plant is cultured, the osmotic pressure increases, water absorption of the plant is hindered, and accordingly, the plant is exposed to the environment which may hinder the growth of the plant. Specifically, for example, this type of stress may be caused when an osmotic potential resulting from a salt in the soil or hydroponic medium is under the condition of 0.2 MPa (2,400 ppm in terms of a NaCl concentration) or higher, strictly 0.25 MPa cr higher, and even more strictly 0.30 MPa or higher. The osmotic pressure in soil may be determined based on the following Raoult's equation, by diluting the soil with water and analyzing a salt concentration of the supernatant liquid.
›MODE FOR CARRYING OUT THE INVENTION · 66 of 73
Laoult's equation
π (atm)= cRT
R=0.082 (L·atm/mol·K)
T=absolute temperature (K)
c=molar concentration of ion (mol/L)
1 atm=0.1 MPa
Production processes of the compound of the present invention is described below.
The compound of the present invention may be prepared according to, for example, the following (Production process 1) to (Production process 18).
(Production Process 1)
A compound represented by Formula (3) may be prepared according to, for example, the following scheme.
[wherein, W 1 represents a hydroxy group, —OR 6 , or —NR 7 R 10 ,
L 1 represents a halogen atom or a nitro group,
R 5a represents a hydrogen atom, a C1-C6 alkyl group optionally having one or more groups selected from the group X, or a phenyl group optionally having one or more groups selected from the group Y, and
R 1 , R 2 , R 3 , R 4 , R 6 , R 7 , and R 10 have the same definition as described above respectively]
This reaction is generally performed in a solvent. Examples of usable solvents include aromatic hydrocarbons such as benzene, toluene, and xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; halogenated hydrocarbons such as dichloromethane, chloroform, and 1,2-dichloroethane; amides such as N,N-dimethylformamide and N,N-dimethylacetamide, sulfones such as sulfolane; and a mixture of these.
In this reaction, a compound represented by Formula (4) is used in an amount of 1 mole or more in general and preferably in an amount of 1 mol to 1.2 moles, based on 1 mole of the compound represented by Formula (2).
Examples of the base used in this reaction include inorganic bases such as sodium carbonate and potassium carbonate; metal alkoxides such as sodium methoxide; alkaline metal hydrides such as sodium hydride; organic bases such as triethylamine, tributylamine, and N,N-diisopropylethylamine; and the like.
In this reaction, the base is used in an amount of 1 mole to 5 moles in general, and preferably in an amount of 1 mole to 1.2 moles, based on 1 mole of the compound represented by Formula (2).
The reaction temperature of this reaction is generally 0° C. to 200° C. and preferably 30° C. to 100° C. The reaction time of this reaction is generally 30 minutes to 30 hours.
The completion of this reaction may be confirmed by sampling a portion of the reaction mixture and using analysis means such as thin-layer chromatography and high-performance liquid chromatography. After this reaction is completed, for example, a post-treatment operation in which acid is added to the reaction mixture, extraction is performed using an organic solvent, and the obtained organic layer is dried and concentrated is performed, whereby the compound represented by Formula (3) may be isolated. The isolated compound that is represented by Formula (3) may also be purified by chromatography, recrystallization, and the like.
(Production Process 2)
The compound represented by Formula (3) may be prepared by according to, for example, the following scheme.
[wherein, L 2 represents a halogen atom, and
W 1 , R 1 , R 2 , R 3 , R 4 , and R 5a have the same definition as described above respectively]
This reaction is generally performed in a solvent. Examples of usable solvents include aromatic hydrocarbons such as benzene, toluene, and xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; halogenated hydrocarbons such as dichloromethane, chloroform, and 1,2-dichloroethane; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfones such as sulfolane, and a mixture of these.
In this reaction, a compound represented by Formula (6) is used in an amount of 1 mole or more in general and preferably in an amount of 1 mole to 2 moles, based on 1 mole of a compound represented by Formula (5).
This reaction is generally performed in the presence of a base. Examples of the base used in this reaction include inorganic bases such as sodium carbonate and potassium carbonate; metal alkoxides such as sodium methoxide; alkaline metal hydrides such as sodium hydride; organic bases such as triethylamine, tributylamine, and N,N-diisopropylethylamine; and the like. In this reaction, the base is used in an amount of 1 mole or more in general, and preferably in an amount of 1 mole to 2 moles, based on 1 mole of the compound represented by Formula (5).
The reaction temperature of this reaction is generally 0° C. to 200° C. and preferably 30° C. to 100° C. The reaction time of this reaction is generally 30 minutes to 30 hours.
The completion of this reaction may be confirmed by sampling a portion of the reaction mixture and using analysis means such as thin-layer chromatography and high-performance liquid chromatography. After this reaction is completed, for example, a post-treatment operation in which water is added to the reaction mixture, extraction is performed using an organic solvent, and the obtained organic layer is dried and concentrated is performed, whereby the compound represented by Formula (3) may be isolated. The isolated compound that is represented by Formula (3) may also be purified by chromatography, recrystallization, and the like.
(Production Process 3)
A compound represented by Formula (8) may be prepared according to, for example, the following scheme.
[wherein, B 1 represents a C1-C6 alkyl group, and PC
L 1 , W 1 , R 1 , R 2 , R 3 , and R 4 have the same definition as described above respectively]
This reaction is generally performed in a solvent. Examples of usable solvents include aromatic hydrocarbons such as benzene, toluene, and xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; halogenated hydrocarbons such as dichloromethane, chloroform, and 1,2-dichloroethane; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfones such as sulfolane, and a mixture of these.
In this reaction, a compound represented by Formula (4) is used in an amount of 1 mole or more in general and preferably in an amount of 1 mole to 1.2 moles, based on 1 mole of a compound represented by Formula (7).
›MODE FOR CARRYING OUT THE INVENTION · 67 of 73
This reaction is generally performed in the presence of a base. Examples of the base used in this reaction include inorganic bases such as sodium carbonate and potassium carbonate; metal alkoxides such as sodium methoxide; alkaline metal hydrides such as sodium hydride; organic bases such as triethylamine, tributylamine, and N,N-diisopropylethylamine; and the like. In this reaction, the base is used in an amount of 1 mole to 5 moles in general, and preferably in an amount of 1 mole to 1.2 moles, based on 1 mole of the compound represented by Formula (7).
The reaction temperature of this reaction is generally 0° C. to 200° C. and preferably 30° C. to 10° C. The reaction time of this reaction is generally 30 minutes to 30 hours.
The completion of this reaction may be confirmed by sampling a portion of the reaction mixture and using analysis means such as thin-layer chromatography and high-performance liquid chromatography. After this reaction is completed, for example, a post-treatment operation in which an acid is added to the reaction mixture, and then the precipitated solids are collected by filtration, washed with water and hexane, and then dried is performed, whereby a compound represented by Formula (8) may be isolated. The isolated compound that is represented by Formula (8) may also be purified by chromatography, recrystallization, and the like.
(Production Process 4)
A compound represented by Formula (10) may be prepared according to, for example, the following scheme.
[wherein, B, L 2 , W 1 , R 1 , R 2 , R 3 , and R 4 have the same definition as described above respectively]
This reaction is generally performed in a solvent. Examples of usable solvents include aromatic hydrocarbons such as benzene, toluene, and xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; halogenated hydrocarbons such as dichloromethane, chloroform, and 1,2-dichloroethane; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfones such as sulfolane, and a mixture of these.
In this reaction, a compound represented by Formula (6) is used in an amount of 1 mole or more in general and preferably in an amount of 1 mole to 2 moles, based on 1 mole of a compound represented by Formula (9).
This reaction is generally performed in the presence of a base. Examples of the base used in this reaction include inorganic bases such as sodium carbonate and potassium carbonate; metal alkoxides such as sodium methoxide; alkaline metal hydrides such as sodium hydride; organic bases such as triethylamine, tributylamine, and N,N-diisopropylethylamine; and the like. In this reaction, the base is used in an amount of 1 mole to 10 moles in general, and preferably in an amount of 1 mole to 2 moles, based on 1 mole of the compound represented by Formula (9).
The reaction temperature of this reaction is generally 0° C. to 200° C. and preferably 30° C. to 100° C. The reaction time of this reaction is generally 30 minutes to 30 hours.
The completion of this reaction may be confirmed by sampling a portion of the reaction mixture and using analysis means such as thin-layer chromatography and high-performance liquid chromatography. After this reaction is completed, for example, a post-treatment operation in which an acid is added to the reaction mixture, and then the precipitated solids are collected by filtration, washed with water and hexane, and then dried is performed, whereby a compound represented by Formula (10) may be isolated. The isolated compound that is represented by Formula (10) may also be purified by chromatography, recrystallization, and the like.
(Production Process 5)
A compound represented by Formula (12) may be prepared by according to, for example, the following scheme.
[wherein, L 1 , W 1 , R 1 , R 2 , R 3 , and R 4 have the same definition as described above respectively]
This reaction is generally performed in a solvent. Examples of usable solvents include aromatic hydrocarbons such as benzene, toluene, and xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; halogenated hydrocarbons such as dichloromethane, chloroform, and 1,2-dichloroethane; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfones such as sulfolane, and a mixture of these.
In this reaction, a compound represented by Formula (4) is used in an amount of 1 mole or more in general and preferably in an amount of 1 mole to 1.2 moles, based on 1 mole of a compound represented by Formula (11).
This reaction is generally performed in the presence of a base. Examples of the base used in this reaction include inorganic bases such as sodium carbonate and potassium carbonate; metal alkoxides such as sodium methoxide; alkaline metal hydrides such as sodium hydride; organic bases such as triethylamine, tributylamine, and N,N-diisopropylethylamine; and the like. In this reaction, the base is used in an amount of 1 mole to 10 moles in general, and preferably in an amount of 1 mole to 1.2 moles, based on 1 mole of the compound represented by Formula (11).
The reaction temperature of this reaction is generally 0° C. to 200° C. and preferably 30° C. to 100° C. The reaction time of this reaction is generally 30 minutes to 30 hours.
The completion of this reaction may be confirmed by sampling a portion of the reaction mixture and using analysis means such as thin-Layer chromatography and high-performance liquid chromatography. After this reaction is completed, for example, water is added to the reaction mixture, extraction is then performed using an organic solvent, and then the obtained organic layer is dried and concentrated, followed by chromatography, recrystallization, and the like, whereby a compound represented by Formula (12) may be isolated.
(Production Process 6)
A compound represented by Formula (14) may be prepared by according to, for example, the following scheme.
[wherein, L 2 , W 1 , R 1 , R 2 , R 3 , and R 4 have the same definition as described above respectively]
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This reaction is generally performed in a solvent. Examples of usable solvents include aromatic hydrocarbons such as benzene, toluene, and xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; halogenated hydrocarbons such as dichloromethane, chloroform, and 1,2-dichloroethane; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfones such as sulfolane, and a mixture of these.
In this reaction, a compound represented by Formula (6) is used in an amount of 1 mole or more in general and preferably in an amount of 1 mol to 2 moles, based on 1 mole of a compound represented by Formula (13).
This reaction is generally performed in the presence of a base. Examples of the base used in this reaction include inorganic bases such as sodium, carbonate and potassium carbonate; metal alkoxides such as sodium methoxide; alkaline metal hydrides such as sodium hydride; organic bases such as triethylamine, tributylamine, and N,N-diisopropylethylamine; and the like. In this reaction, the base is used in an amount of 1 mole to 5 moles in general, and preferably in an amount of 1 mole to 2 moles, based on 1 mole of the compound represented by Formula (13).
The reaction temperature of this reaction is generally 0° C. to 200° C. and preferably 30° C. to 100° C. The reaction time of this reaction is generally 30 minutes to 30 hours.
The completion of this reaction may be confirmed by sampling a portion of the reaction mixture and using analysis means such as thin-layer chromatography and high-performance liquid chromatography. After this reaction is completed, for example, water is added to the reaction mixture, extraction is then performed using an organic solvent, and then the obtained organic layer is dried and concentrated, followed by chromatography, recrystallization, and the like, whereby a compound represented by Formula (14) may be isolated.
(Production Process 7)
A compound represented by Formula (16) may be prepared by according to, for example, the following scheme.
[wherein, L 3 represents a leaving group (for example, a halogen atom such as a chlorine atom, a bromine atom, or an iodine atom, and the pseudohalogen) substituted at position 3, 4, 5, 6, or 7, B 2 represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, a C2-C6 alkenyl group optionally having one or more groups selected from the group X, a C2-C6 alkynyl group which may have optionally one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, or a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and W 1 has the same definition as described above]
In this reaction, a compound represented by Formula (17) is used in an amount of 1 mole or more in general, and preferably in an amount of 1 mole to 3 moles, based on 1 mol of a compound represented by (15).
This reaction is performed in a solvent. Examples of the solvent used in this reaction include aromatic hydrocarbons such as benzene, toluene, and xylene; alcohols such as methanol, ethanol, and propanol; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; ketones such as acetone and methyl ethyl ketone; nitriles such as acetonitrile; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfoxides such as dimethyl sulfoxide; sulfones such as sulfolane; water; and a mixture of these.
Moreover, this reaction is performed in the presence of a base. Examples of the base used in this reaction include organic bases such as triethylamine, tripropylamine, pyridine, dimethylaniline, dimethylaminopyridine, and 1,8-diazabicyclo[5.4.0]-7-undecene; and inorganic bases such as sodium hydroxide, potassium hydroxide, calcium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogen carbonate, calcium carbonate, cesium carbonate, and potassium phosphate. In this reaction, the base is used in an amount of 0.5 mole to 10 moles in general, and preferably in an amount of 1 mole to 5 moles, based on 1 mole of the compound represented by Formula (15).
This reaction is generally performed in the presence of a catalyst such as tetrakis(triphenylphosphine)palladium (0), dichlorobis(triphenylphosphine)palladium (II), dichlorobis(tricyclohexylphosphine)palladium (II), or a [1,1′-bis(diphenylphosphino)ferrocene palladium] (II) dichloride dichloromethane adduct. This catalyst is used in an amount of 0.001 moles to 0.5 moles in general and preferably in an amount of 0.01 moles to 0.2 moles, based on 1 mol of the compound represented by Formula (15).
In this reaction, lithium chloride or the like is optionally used in an amount of 1 mole to 20 moles and preferably in an amount of 2 mole to 10 moles, based on 1 mole of the compound represented by Formula (15).
The reaction temperature of this reaction is generally 20° C. to 180° C. and preferably 60° C. to 150° C. The reaction time of this reaction is generally 30 minutes to 100 hours. The progress of this reaction may be confirmed by analyzing a portion of the reaction mixture by thin-layer chromatography, high-performance liquid chromatography, and the like.
After this reaction is completed, for example, an operation in which the reaction mixture is mixed with water, extraction is performed using an organic solvent, and the obtained organic layer is dried and concentrated is performed, whereby the compound represented by Formula (16) may be isolated. The isolated compound that is represented by Formula (16) may also be purified by chromatography, recrystallization, and the like.
(Production Process 8)
A compound represented by Formula (19) may be prepared according to, for example, the following scheme.
[wherein, B 3 represents a C2-C6 alkenyl group optionally having one or more groups selected from the group X, a C2-C6 alkynyl group optionally having one or more groups selected from the group X, a phenyl group optionally having one or more groups selected from the group Y, a 6-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, or a 5-membered aromatic heterocyclic group optionally having one or more groups selected from the group Y, and
›MODE FOR CARRYING OUT THE INVENTION · 69 of 73
B 1 , L 3 , and W 1 have the same definition as described above respectively]
In this reaction, a compound represented by Formula (20) is used in an amount of 1 mole or more in general, and preferably in an amount of 1 mole to 3 moles, based on 1 mole of a compound represented by Formula (18).
This reaction is performed in a solvent. Examples of the solvent used in this reaction include aromatic hydrocarbons such as benzene, toluene, and xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfoxides such as dimethyl sulfoxide; and a mixture of these.
This reaction is generally performed in the presence of a catalyst such as tetrakis(triphenylphosphine)palladium (0) or dichlorobis(triphenylphosphine)palladium (II). This catalyst is used in an amount of 0.001 moles to 0.5 moles in general, and preferably in an amount of 0.01 moles to 0.2 moles, based on 1 mole of the compound represented by Formula 18).
The reaction temperature of this reaction is generally −80° C. to 180° C. and preferably −30° C. to 150#C. The reaction time of this reaction is generally 30 minutes to 100 hours. The progress of this reaction may be confirmed by analyzing a portion of the reaction mixture by thin-layer chromatography, high-performance liquid chromatography, and the like. After this reaction is completed, for example, an operation in which the reaction mixture is mixed with water, extraction is performed using an organic solvent, and the obtained organic layer is dried and concentrated is performed, whereby the compound represented by Formula (19) may be isolated. The isolated compound that is represented by Formula (19) may also be purified by chromatography, recrystallization, and the like.
(Production Process 9)
A compound represented by Formula (22) may be prepared according to, for example, the following scheme.
[wherein, HO represents a hydroxy group substituted at a position 3, 4, 5, 6, or 7,
R 11a represents a C1-C6 alkyl group optionally having one or more groups selected from the group X, a C3-C6 alkenyl group optionally having one or more groups selected from the group X, a C3-C6 alkynyl group optionally having one or more groups selected from the group X, a C4-C7 cycloalkylalkyl group optionally having one or more halogen atoms, a C7-C9 phenylalkyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y, a 6-membered aromatic heterocyclic-C1-C3 alkyl group wherein a 6-membered aromatic heterocyclic portion may have optionally one or more groups selected from the group Y, or a C3-C6 cycloalkyl group optionally having one or more halogen atoms, and
W 1 and L 2 have the same definition as described above respectively]
This reaction is performed in a solvent. Examples of the solvent used in this reaction include aromatic hydrocarbons such as benzene, toluene, and xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; halogenated hydrocarbons such as dichloromethane, chloroform, and 1,2-dichloroethane; ketones such as acetone and methyl ethyl ketone; nitriles such as acetonitrile; esters such as ethyl acetate; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfoxides such as dimethyl sulfoxide; sulfones such as sulfolane; and a mixture of these.
In this reaction, a compound represented by Formula (23) is used in an amount of 1 mole or more in general, and preferably in an amount of 1 mole to 3 moles, based on 1 mole of the compound represented by Formula (21).
This reaction is generally performed in the presence of a base. Examples of the base used in this reaction include organic bases such as triethylamine, tripropylamine, pyridine, dimethylaminopyridine, and 1,8-diazabicyclo[5.4.0]-7-undecene; inorganic bases such as sodium hydroxide, potassium hydroxide, calcium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogen carbonate, and calcium carbonate; metal hydrides such as sodium hydride; and metal alkoxides such as sodium methylate, sodium ethylate, and potassium t-butoxide. In this reaction, the base is used in an amount of 0.5 molar equivalents to 10 molar equivalents in general, and preferably in an amount of 1 molar equivalent to 5 molar equivalents, based on 1 mole of the compound represented by Formula (21).
The reaction temperature of this reaction is generally −30° C. to 180° C. and preferably 0° C. to 100° C. The reaction time of this reaction is generally 10 minutes to 30 hours.
The progress of this reaction may be confirmed by analyzing a portion of the reaction mixture by thin-layer chromatography, high-performance liquid chromatography, and the like. After this reaction is completed, for example, an operation in which the reaction mixture is mixed with water, extraction is performed using an organic solvent, and the obtained organic layer is dried and concentrated is performed, whereby the compound represented by Formula (22) may be isolated. The isolated compound that is represented by Formula (22) may also be purified by chromatography, recrystallization, and the like.
(Production Process 10)
A compound represented by Formula (25) may be prepared according to, for example, the following scheme.
[wherein, H 2 N represents an amino group substituted at a position 3, 4, 5, 6, or 7,
R 12a represents a C1-C4 alkyl group optionally having one or more halogen atoms, a C1-C4 alkylsulfonyl group optionally having one or more halogen atoms, a phenylsulfonyl group optionally having one or more groups selected from the group Y, a C7-C9 phenylalkylsulfonyl group wherein a benzene ring portion may have optionally one or more groups selected from the group Y, a C2-C6 alkoxycarbonyl group, —C(O)R 15 , or —C(O)NR 7 R 8 , and
W 1 , L 2 , R, R 8 , and R 15 have the same definition as described above respectively]
This reaction may be performed in a solvent. Examples of the usable solvent include aromatic hydrocarbons such as benzene, and toluene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; halogenated hydrocarbons such as dichloromethane, chloroform, and 1,2-dichloroethane; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfoxides such as dimethyl sulfoxide; sulfones such as sulfolane; and a mixture of these.
›MODE FOR CARRYING OUT THE INVENTION · 70 of 73
The amount of a compound represented by Formula (26) used in this reaction is generally 1 molar equivalent or more, and preferably 1 molar equivalent to 3 molar equivalents, based on the compound represented by Formula (24).
This reaction is generally performed in the presence of a base. Examples of the base used in this reaction include organic bases such as triethylamine, tripropylamine, pyridine, dimethylaminopyridine, diisopropyl ethylamine, and 1,8-diazabicyclo[5.4.0]-7-undecene; and inorganic bases such as sodium hydroxide, potassium hydroxide, calcium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogen carbonate, calcium carbonate, and sodium hydride. In this reaction, the base is used in an amount of 0.5 moles to 10 moles in general, and preferably in an amount of 1 mole to 5 moles, based on 1 mole of the compound represented by Formula (24).
The reaction temperature of this reaction is generally −30° C. to 180° C. and preferably −10° C. to 50° C. The reaction time of this reaction is generally 10 minutes to 30 hours.
The completion of this reaction may be confirmed by sampling a portion of the reaction mixture and using analysis means such as thin-layer chromatography and high-performance liquid chromatography. After this reaction is completed, for example, an operation in which the reaction mixture is mixed with water, extraction is performed using an organic solvent, and the obtained organic layer is dried and concentrated is performed, whereby the compound represented by Formula (25) may be isolated. The isolated compound that is represented by Formula (25) may also be purified by chromatography, recrystallization, and the like.
(Production Process 11)
A compound represented by Formula (28) may be prepared according to, for example, the following scheme.
[wherein, R 1 , R 2 , R 3 , R 4 , and R 5 have the same definition as described above respectively]
This reaction is generally performed in a solvent. Examples of the usable solvent include aromatic hydrocarbons such as benzene, toluene, and xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; and a mixture of these.
This reaction is performed in the presence of a base. Examples of the base used in this reaction include n-butyllithium, lithium diisopropylamide, and the like. In this reaction, the base is used in an amount of 1 mole to 2 moles in general, and preferably in an amount of 1 mole to 1.1 moles, based on 1 mole of a compound represented by Formula (27).
In this reaction, the compound represented by Formula (29) is used in an amount of 10 moles or more in general, and preferably in an amount of 10 moles to 1,000 moles, based on 1 mol of the compound represented by Formula (27).
The reaction temperature of this reaction is generally −100° C. to 0° C., and the reaction time of this reaction is generally 5 minutes to 5 hours.
The completion of this reaction may be confirmed by sampling a portion of the reaction mixture and using analysis means such as thin-layer chromatography and high-performance liquid chromatography. After this reaction is completed, for example, an operation in which water is added to the reaction mixture, the residue is washed with an organic solvent, concentrated hydrochloric acid is then added to the aqueous layer, extraction is performed using an organic solvent, and the obtained organic layer is dried and concentrated is performed, whereby the compound represented by Formula (28) may be isolated.
(Production Process 12)
A compound represented by Formula (30) may be prepared according to, for example, the following scheme.
[wherein, L 2 , R 1 , R 2 , R 3 , R 4 , and R 5 have the same definition as described above respectively]
This reaction is generally performed in a solvent. Examples of the usable solvent include aromatic hydrocarbons such as benzene and toluene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; halogenated hydrocarbons such as dichloromethane, chloroform, and 1,2-dichloroethane; sulfoxides such as dimethyl sulfoxide, sulfones such as sulfolane; and a mixture of these.
Examples of the electrophilic halogenation agent used in this reaction include thionyl chloride, oxalyl chloride, phosphoryl chloride, sulfuryl chloride, phosphorus trichloride, phosphorus pentachloride, phosphorus tribromide, phosgene, and the like.
In this reaction, the electrophilic halogenation agent is used in an amount of 1 mole to 100 moles in general, and preferably in an amount of 2 moles to 20 moles, based on 1 mole of a compound represented by Formula (28).
In this reaction, N,N-dimethylformamide and the like are also optionally used in an amount of 0.001 moles to 1,000 moles, and preferably in an amount of 0.01 moles to 50 moles, based on 1 mole of the compound represented by Formula (28). The reaction temperature of this reaction is generally in a range of room temperature to a boiling point of the solvent used, preferably 60° C. to a boiling point of the solvent. This reaction may be performed in a sealed tube or a pressure-resistant sealed container.
The reaction time of this reaction is generally about 5 minutes to several days.
The progress of this reaction may be confirmed by analyzing a portion of the reaction mixture by thin-layer chromatography, high-performance liquid chromatography, and the like. After this reaction is completed, for example, an operation in which the reaction mixture is concentrated is performed, whereby the compound represented by Formula (30) may be isolated.
(Production Process 13)
The compound represented by Formula (1) may be prepared by according to, for example, the following scheme.
[wherein, W, L 2 , R 1 , R 2 , R 3 , R 4 , and R 5 have the same definition as described above respectively]
This reaction is generally performed in a solvent. Examples of usable solvents include aromatic hydrocarbons such as benzene, toluene, and xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; halogenated hydrocarbons such as dichloromethane, chloroform, and 1,2-dichloroethane; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfones such as sulfolane; ketones such as acetone, methyl ethyl ketone, and methyl isobutyl ketone; and a mixture of these.
›MODE FOR CARRYING OUT THE INVENTION · 71 of 73
In this reaction, a compound represented by Formula (31) is used in an amount of 1 mole or more in general, and preferably in an amount of 1 mole to 50 moles, based on 1 mole of a compound represented by Formula (30).
This reaction is generally performed in the presence of a base. Examples of the base used in this reaction include metal carbonates such as sodium carbonate and potassium carbonate; metal alkoxides such as sodium methoxide; alkaline metal hydrides such as sodium hydride; organic bases such as triethylamine, tributylamine, and N,N-diisopropylethylamine; and the like.
In this reaction, the base is used in an amount of 1 mole to 50 moles in general, and preferably in an amount of 1 mole to 5 moles, based on 1 mole of the compound represented by Formula (30).
The reaction temperature of this reaction is generally 0° C. to 200° C. and preferably 30° C. to 100° C. The reaction time of this reaction is generally 30 minutes to 30 hours.
The completion of this reaction may be confirmed by sampling a portion of the reaction mixture and using analysis means such as thin-layer chromatography and high-performance liquid chromatography. After this reaction is completed, for example, a post-treatment operation in which water is added to the reaction mixture, extraction is performed using an organic solvent, and the obtained organic layer is dried and concentrated is performed, whereby the compound represented by Formula (1) may be isolated. The isolated compound that is represented by Formula (1) may also be purified by chromatography, recrystallization, and the like.
(Production Process 14)
Among the compounds of the present invention, the compound represented by Formula (1) may be prepared according to the following scheme.
[wherein, W, R 1 , R 2 , R 3 , R 4 , and R 5 have the same definition as described above respectively]
This reaction is generally performed in a solvent. Examples of usable solvents include aromatic hydrocarbons such as benzene, toluene, and xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; halogenated hydrocarbons such as dichloromethane, chloroform, and 1,2-dichloroethane; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfones such as sulfolane; esters such as ethyl acetate and butyl acetate; and a mixture of these.
In this reaction, a compound represented by Formula (31) is used in an amount of 1 mole or more in general, and preferably in an amount of 1 mole to 10 moles, based on 1 mole of the compound represented by Formula (28).
Examples of the dehydration-condensation agent used in this reaction include carbodiimide-based agents such as N,N-dicyclohexylcarbodiimide, and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride; phosphonium salt-based agents such as a benzotriazol-1-yloxytris(dimethylamino)phosphonium salt; and the like.
In this reaction, the dehydration-condensation agent is used in an amount of 1 mole to 50 moles in general, and preferably in an amount of 1 mole to 10 moles, based on 1 mole of the compound represented by Formula (28).
In this reaction, 4,4-dimethylaminopyridine and the like are also optionally used in an amount of 0.001 moles to 10 moles, and preferably in an amount of 0.01 moles to 0.5 moles, based on 1 mole of the compound represented by Formula (28).
This reaction is optionally performed in the presence of a base. Examples of the base used in this reaction include metal carbonate such as sodium carbonate and potassium carbonate; metal alkoxides such as sodium methoxide; alkaline metal hydrides such as sodium hydride; organic bases such as triethylamine, tributylamine, and N,N-diisopropylethylamine; and the like. These bases are used in an amount of 1 mole to 50 moles in general, and preferably in an amount of 1 mole to 10 moles, based on 1 mole of the compound represented by Formula (28).
The reaction temperature of this reaction is generally 0° C. to 200° C. and preferably 30° C. to 100° C. The reaction time of this reaction is generally 30 minutes to 30 hours.
The completion of this reaction may be confirmed by sampling a portion of the reaction mixture and using analysis means such as thin-layer chromatography and high-performance liquid chromatography. After this reaction is completed, for example, a post-treatment operation in which water is added to the reaction mixture, extraction is performed using an organic solvent, and the obtained organic layer is dried and concentrated is performed, whereby the compound represented by Formula (1) may be isolated. The isolated compound that is represented by Formula (1) may also be purified by chromatography, recrystallization, and the like.
(Production Process 15)
A compound represented by Formula (33) may be prepared according to, for example, the following scheme.
[wherein, I 1 represents an iodine atom substituted at a position 3, 4, 5, 6, or 7,
B 4 represents a C1-C6 alkyl group optionally having one or more halogen atoms, and
W has the same definition as described above]
In this reaction, a compound represented by Formula (34) is used in an amount of 2 moles or more in general, and preferably in an amount of 2 moles to 20 moles, based on 1 mole of a compound represented by Formula (32).
This reaction is performed in a solvent. Examples of the solvent used in this reaction include aromatic hydrocarbons such as benzene, toluene, and xylene; amides such as N,N-dimethylformamide, N,N-dimethylacetamide, and N-methyl-2-pyrrolidone; sulfoxides such as dimethyl sulfoxide; and a mixture of these.
This reaction is generally performed in the presence of a catalyst such as copper (I) iodide. In this reaction, the catalyst is used in an amount of 1 mole or more in general, and preferably in an amount of 1 mole to 10 moles, based on 1 mole of the compound represented by Formula (32).
The reaction temperature of this reaction is generally 0° C. to 300° C. and preferably 120° C. to 250° C. The reaction time of this reaction is generally 30 minutes to 100 hours. The progress of this reaction may be confirmed by analyzing a portion of the reaction mixture by thin-layer chromatography, high-performance liquid chromatography, and the like.
›MODE FOR CARRYING OUT THE INVENTION · 72 of 73
After this reaction is completed, an operation such as silica gel chromatography is performed, whereby a compound represented by Formula (33) may be isolated.
(Production Process 16)
A compound represented by Formula (33) may be prepared according to, for example, the following scheme.
[wherein, I 1 , B 4 , and W 2 have the same definition as described above respectively]
In this reaction, a compound represented by Formula (35) is used in an amount of 1 mole or more in general, and preferably in an amount of 1 mole to 20 moles, based on 1 mole of the compound represented by Formula (32).
This reaction is performed in a solvent. Examples of the solvent used in this reaction include aromatic hydrocarbons such as benzene, toluene, and xylene; amides such as N,N-dimethylformamide, N,N-dimethylacetamide, and N-methyl-2-pyrrolidone; sulfoxides such as dimethyl sulfoxide; and a mixture of these.
This reaction is generally performed in the presence of a catalyst such as copper (0). In this reaction, the catalyst is used in an amount of 1 mole or more in general, and preferably in an amount of 1 mole to 20 moles, based on 1 mole of the compound represented by Formula (32).
The reaction temperature of this reaction is generally 0° C. to 300° C. and preferably 120° C. to 250° C. The reaction time of this reaction is generally 30 minutes to 100 hours. The progress of this reaction may be confirmed by analyzing a portion of the reaction mixture by thin-layer chromatography, high-performance liquid chromatography, and the like.
After this reaction is completed, an operation such as silica gel chromatography is performed, whereby the compound represented by Formula (33) may be isolated.
(Production Process 17)
A compound represented by Formula (36) may be prepared by, for example, reacting (15) with (37) in the presence of a palladium compound, a base, and a copper salt.
[wherein, B 5 represents a hydrogen atom, a C1-C4 alkyl group optionally having one or more groups selected from the group X, or a trimethylsilyl group, and W 1 and L 3 have the same definition as described above respectively]
In this reaction, the compound represented by Formula (37) is used in an amount of 1 mole or more, and preferably in an amount of 1 mole to 10 moles, based on 1 mole of the compound represented by Formula (15).
This reaction is generally performed using a base as a solvent. However, an auxiliary solvent may also be used.
Examples of the base used in this reaction include organic bases such as triethylamine, diethylamine, diisopropylamine, tripropylamine, pyridine, dimethylaniline, dimethylaminopyridine, and 1,8-diazabicyclo[5.4.0]-7-undecene. In this reaction, the base is used in an amount of 1 mole to 1,000 moles in general, and preferably in an amount of 1 mole to 100 moles, based on 1 mole of the compound represented by (15).
Examples of the auxiliary solvent used in this reaction include aromatic hydrocarbons such as benzene, toluene, xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; nitriles such as acetonitrile; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfoxides such as dimethyl sulfoxide; sulfones such as sulfolane; and a mixture of these.
Examples of the palladium compound used in this reaction include tetrakis(triphenylphosphine)paladium, dichlorobis(triphenylphosphine)palladium, dichlorobis(tricyclohexylphosphine)palladium, or a [1,1′-bis(diphenylphosphino)ferrocene]palladium (II) dichloride dichloromethane adduct. In this reaction, the palladium compound is used in an amount of 0.001 moles or more, and preferably in an amount of 0.001 moles to 0.5 moles, based on 1 mole of the compound represented by Formula (15).
Examples of the copper salt used in this reaction include copper (I) iodide, copper (I) bromide, and the like. In this reaction, the copper salt is used in an amount of 0.001 moles or more and preferably in an amount of 0.031 moles to 0.5 moles, based on 1 mole of the compound represented by Formula (15).
The reaction temperature of this reaction is generally 0° C. to 180° C. and preferably 10° C. to 100° C. The reaction time of this reaction is generally 30 minutes to 100 hours. The progress of this reaction may be confirmed by analyzing a portion of the reaction mixture by thin-layer chromatography, high-performance liquid chromatography, and the like. After this reaction is completed, for example, an operation in which water is added to the reaction mixture, extraction is performed using an organic solvent, and the obtained organic layer is dried and concentrated is performed, whereby the compound represented by Formula (36) may be isolated. The isolated compound that is represented by Formula (36) may also be purified by chromatography, recrystallization, and the like.
Moreover, a compound represented by Formula (37) wherein B 5 represents a trimethylsilyl group is reacted with the compound (15) in the presence of a palladium compound, a base, and a copper salt, and a desilylation reaction is performed on the compound obtained by the above reaction based on the method described in “GREENE'S PROTECTIVE GROUPS IN ORGANIC SYNTHESIS Fourth Edition, Wiley Interscience, 2007”, whereby a compound represented by Formula (36) wherein B 5 represents a hydrogen atom may be obtained.
The compound represented by Formula (16) may be prepared according to, for example, the following scheme.
(Production Process 18)
[wherein, —B(OH) 2 represents —B(OH) 2 substituted at a position 3, 4, 5, 6, or 7, and B 2 , L 2 , and W 1 have the same definition as described above respectively]
In this reaction, a compound represented by Formula (39) is used in an amount of 1 mole or more, and preferably in an amount of 1 mole to 3 moles, based on 1 mole of a compound represented by Formula (38).
This reaction is performed in a solvent. Examples of the solvent used in this reaction include aromatic hydrocarbons such as benzene, toluene, and xylene; alcohols such as methanol, ethanol, and propanol; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; ketones such as acetone, methyl ethyl ketone, and methyl isobutyl ketone; nitriles such as acetonitrile; amides such as N,N-dimethylformamide and N,N-dimethylacetamide; sulfoxides such as dimethyl sulfoxide; sulfones such as sulfolane; water; and a mixture of these.
›MODE FOR CARRYING OUT THE INVENTION · 73 of 73
Moreover, this reaction is performed in the presence of a base. Examples of the base used in this reaction include organic bases such as triethylamine, tripropylamine, pyridine, dimethylaniline, dimethylaminopyridine, and 1,8-diazabicyclo[5.4.0]-7-undecene; and inorganic bases such as sodium hydroxide, potassium hydroxide, calcium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogen carbonate, calcium carbonate, cesium carbonate, and potassium phosphate. In this reaction, the base is used in an amount of 0.5 moles to 10 moles in general, and preferably in an amount of 1 mole to 5 moles, based on 1 mole of the compound represented by Formula (38).
This reaction is generally performed in the presence of a catalyst such as tetrakis(triphenylphosphine)palladium, dichlorobis(triphenylphosphine)palladium, dichlorobis(tricyclohexylphosphine)palladium, or a [1,1′-bis(diphenylphosphino)ferrocene]palladium (II) dichloride dichloromethane adduct. In this reaction, the catalyst is used in an amount of 0.001 moles to 0.5 moles, and preferably in an amount of 0.01 moles to 0.2 moles, based on 1 mole of the compound represented by Formula (38).
In this reaction, lithium chloride or the like is optionally used in an amount of 1 mole to 20 moles, and preferably in an amount of 2 moles to 10 moles, based on 1 mole of the compound represented by (38).
The reaction temperature of this reaction is generally 20° C. to 180° C. and preferably 60° C. to 150° C. The reaction time of this reaction is generally 30 minutes to 100 hours. The progress of this reaction may be confirmed by analyzing a portion of the reaction mixture by thin-layer chromatography, high-performance liquid chromatography, and the like.
After this reaction is completed, for example, an operation in which the reaction mixture is mixed with water, extraction is performed using an organic solvent, and the obtained organic layer is dried and concentrated is performed, whereby the compound represented by Formula (16) may be isolated. The isolated compound that is represented by Formula (16) may also be purified by chromatography, recrystallization, and the like.
Reference Production Process 1
The compound represented by Formula (2) may be prepared according to, for example, the following scheme.
[wherein, L 4 represents a leaving group (for example, a halogen atom such as a chlorine atom, a bromine atom, or an iodine atom, a C1-C6 alkoxy group such as a methoxy group or an ethoxy group, and an N-methoxy-N-methylamino group), and L 1 , R 1 , R 2 , R 3 , R 4 , and R 5a have the same definition as described above respectively]
This reaction is generally performed in a solvent. Examples of the usable solvent include aromatic hydrocarbon such as benzene, toluene, and xylene; ethers such as diethylether, diisopropylether, 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; and a mixture of these.
This reaction is performed in the presence of a base. Examples of the base used in this reaction include n-butyllithium, lithium isopropylamide, and the like. In this reaction, the base is used in an amount of 1 mole to 2 moles in general, and preferably in an amount of 1 mole to 1.1 moles, based on 1 mole of the compound represented by Formula (40).
In this reaction, the compound represented by Formula (41) is used in an amount of 1 mole or more in general, and preferably in an amount of 1 mole to 10 moles, based on 1 mole of the compound represented by Formula (40).
The reaction temperature of this reaction is generally −100° C. to −30° C., and the reaction time of this reaction is generally 5 minutes to 5 hours.
The completion of this reaction may be confirmed by sampling a portion of the reaction mixture and using analysis means such as thin-layer chromatography and high-performance liquid chromatography. After this reaction is completed, for example, water is added to the reaction mixture, extraction is performed using an organic solvent, the obtained organic layer is dried and concentrated, and then chromatography, distillation, and the like are performed, whereby the compound represented by (2) may be isolated.
Reference Production Process 2
A compound represented by Formula (42) may be prepared by, for example, reacting the compound represented by Formula (1) with a metal hydroxide.
[wherein, W, R 1 , R 2 , R 3 , R 4 , and R 5 have the same
›Tables in the description — 16
| present | Melting | ||||||
| invention | R 1 | R 2 | R 3 | R 4 | R 5 | W | point |
| 1 | H | H | H | H | H | MeO— | 68.1° C. |
| 2 | F | H | H | H | H | MeO— | 95.6° C. |
| 3 | H | F | H | H | H | MeO— | * |
| 4 | H | H | F | H | H | MeO— | 91.5° C. |
| 5 | H | H | H | B | H | MeO— | 84.0° C. |
| 6 | Cl | H | H | H | B | MeO— | 89.4° C. |
| 7 | H | Cl | H | H | H | MeO— | — |
| 8 | H | H | Cl | H | H | MeO— | 100.8° C. |
| 9 | H | H | H | Cl | H | MeO— | 82.1° C. |
| 10 | H | H | H | H | Cl | MeO— | * |
| 11 | Br | H | H | H | H | MeO— | * |
| 12 | H | Br | H | H | H | MeO— | * |
| 13 | H | H | Br | H | H | MeO— | * |
| 14 | H | H | H | Br | H | MeO— | * |
| 15 | I | H | H | H | H | MeO— | * |
| 16 | H | I | H | H | H | MeO— | * |
| 17 | H | CN | H | H | H | MeO— | * |
| 18 | NO 2 | H | H | H | H | MeO— | * |
| 19 | H | NO 2 | H | H | H | MeO— | * |
| 20 | H | H | NO 2 | H | H | MeO— | * |
| 21 | H | H | H | H | NO 2 | MeO— | 104.8° C. |
| 22 | Me | H | H | H | H | MeO— | — |
| 23 | H | Me | H | H | H | MeO— | — |
| 24 | H | H | Me | H | H | MeO— | * |
| 25 | H | H | H | Me | H | MeO— | — |
| present | Melting | ||||||
| invention | R 1 | R 2 | R 3 | R 4 | R 5 | W | point |
| 26 | H | H | H | H | Me | MeO— | 103.1° C. |
| 27 | H | t Bu | H | H | H | MeO— | — |
| 28 | H | H | H | H | CF 3 | MeO— | — |
| 29 | C 2 F 5 | H | H | H | H | MeO— | — |
| 30 | H | C 2 F 5 | H | H | H | MeO— | — |
| 31 | H | C 3 F 7 | H | H | H | MeO— | — |
| 32 | H | H | H 2 C═CH— | H | H | MeO— | — |
| 33 | H | H | HC≡C— | H | H | MeO— | — |
| 34 | Ph | H | H | H | H | MeO— | — |
| 35 | H | Ph | H | H | H | MeO— | — |
| 36 | H | H | Ph | H | H | MeO— | — |
| 37 | H | H | H | Ph | H | MeO— | — |
| 38 | H | H | H | H | Ph | MeO— | — |
| 39 | H | (2-Cl)Ph— | H | H | H | MeO— | — |
| 40 | H | (3-Cl)Ph— | H | H | H | MeO— | — |
| 41 | H | (4-Cl)Ph— | H | H | H | MeO— | — |
| 42 | H | H | H | (3-Me)Ph— | H | MeO— | — |
| 43 | H | (4-CF 3 )Ph— | H | H | H | MeO— | — |
| 44 | H | H | H | (2-MeO)Ph— | H | MeO— | — |
| 45 | H | H | (4-CF 3 O)Ph— | H | H | MeO— | — |
| 46 | H | 2-pyridyl | H | H | H | MeO— | — |
| 47 | H | 3-pyridyl | H | H | H | MeO— | — |
| 48 | H | 4-pyridyl | H | H | H | MeO— | — |
| 49 | H | H | 6-(trifluoromethyl)-3-pyridyl- | H | H | MeO— | — |
| 50 | H | 2-pyrimidinyl- | H | H | H | MeO— | — |
| present | Melting | ||||||
| invention | R 1 | R 2 | R 3 | R 4 | R 5 | W | point |
| 51 | H | H | H | H | 1-pyrrolyl- | MeO— | 114.4° C. |
| 52 | 2-thienyl- | H | H | H | H | MeO— | — |
| 53 | H | 2-thienyl- | H | H | H | MeO— | — |
| 54 | H | MeC(O)— | H | H | H | MeO— | — |
| 55 | H | CF 3 C(O)— | H | H | H | MeO— | — |
| 56 | H | PhC(O)— | H | H | H | MeO— | — |
| 57 | MeOC(O)— | H | H | H | H | MeO— | — |
| 58 | H | MeOC(O)— | H | H | H | MeO— | — |
| 59 | H | H | MeOC(O)— | H | H | MeO— | * |
| 60 | H | H | H | H | MeOC(O)— | MeO— | — |
| 61 | H | NH 2 C(O)— | H | H | H | MeO— | — |
| 62 | NH 2 | H | H | H | H | MeO— | * |
| 63 | H | NH 2 | H | H | H | MeO— | * |
| 64 | H | H | NH 2 | H | H | MeO— | * |
| 65 | H | H | H | H | NH 2 | MeO— | * |
| 66 | Me 2 N— | H | H | H | H | MeO— | — |
| 67 | H | MeC(O)NH— | H | H | H | MeO— | — |
| 66 | H | PhC(O)NH— | H | H | H | MeO— | — |
| 69 | H | H | H | H | HC(O)NH— | MeO— | — |
| 70 | H | H | H | H | MeC(O)NH— | MeO— | — |
| 71 | H | CF 3 C(O)NH— | H | H | H | MeO— | — |
| 72 | H | ClCH 2 C(O)NH 2 — | H | H | H | MeO— | — |
| 73 | H | H | H | H | PhC(O)NH— | MeO— | 146.1° C. |
| 74 | H | H | H | H | [(3-methyl-5- | MeO— | 208.0° C. |
| isoxazolyl) | (decomp.) | ||||||
| carbonyl]amino- | |||||||
| 75 | H | H | H | H | [(1-methyl-1H- | MeO— | 191.6° C. |
| pyrazol-3yl) | |||||||
| carbonyl]amino- |
| present | Melting | ||||||
| invention | R 1 | R 2 | R 3 | R 4 | R 5 | W | point |
| 76 | H | H | H | H | [(1,4-dimethyl-1H-pyrazol- | MeO— | 201.9° C. |
| 5-yl)carbonyl]amino- | (decomp.) | ||||||
| 77 | H | H | H | H | [(1,5-dimethyl-1H-pyrazol- | MeO— | 157.7° C. |
| 3-yl)carbonyl]amino- | |||||||
| 78 | H | (2-thienyl) | H | H | H | MeO— | 217.6° C. |
| C(O)NH— | |||||||
| 79 | H | H | H | H | [3-(2.5-dichlorothienyl)] | MeO— | 169.9° C. |
| C(O)NH— | |||||||
| 80 | H | H | H | H | [2-(5-Bromothienyl)]C(O)NH— | MeO— | 136.3° C. |
| 81 | H | MeSO 2 NH— | H | H | H | MeO— | — |
| 82 | H | BnSO 2 NH— | H | H | H | MeO— | 156.1° C. |
| 83 | H | CF 3 SO 2 NH—— | H | H | H | MeO— | — |
| 84 | H | (4-Cl—Ph)SO 2 NH— | H | H | H | MeO— | * |
| 85 | H | (4-Me—Ph)SO 2 NH— | H | H | H | MeO— | * |
| 86 | H | OH | H | H | H | MeO— | * |
| 87 | H | H | OH | H | H | MeO— | * |
| 88 | H | H | H | OH | H | MeO— | * |
| 89 | H | H | H | H | OH | MeO— | * |
| 90 | MeO— | H | H | H | H | MeO— | * |
| 91 | H | MeO— | H | H | H | MeO— | * |
| 92 | H | H | MeO— | H | H | MeO— | * |
| 93 | H | H | H | MeO— | H | MeO— | * |
| 94 | H | H | H | H | MeO— | MeO— | — |
| 95 | H | H | H | H | EtO— | MeO— | — |
| 96 | H | H | H | H | iPrO— | MeO— | — |
| 97 | H | H | H | H | BnO— | MeO— | — |
| 98 | H | CF 3 O— | H | H | H | MeO— | — |
| 99 | H | H | HC≡CCH 2 O— | H | H | MeO— | — |
| 100 | H | H | (4-CF 3 Bn)O— | H | H | MeO— | — |
| the present | Melting | ||||||
| invention | R 1 | R 2 | R 3 | R 4 | R 5 | W | point |
| 101 | H | H | (3-MeOBn)O— | H | H | MeO— | — |
| 102 | H | H | H | (2-Me)PhO— | H | MeO— | — |
| 103 | H | H | H | (4-CF 3 )PhO— | H | MeO— | — |
| 104 | H | H | H | (4-CF 3 O)PhO— | H | MeO— | — |
| 105 | H | H | H | H | MeC(O)O— | MeO— | — |
| 106 | H | H | H | H | (2-ClPh)C(O)O— | MeO— | 150.6° C. |
| 107 | H | H | H | H | (4-MePh)S(O) 2 O— | MeO— | 154.9° C. |
| 108 | H | MeS— | H | H | H | MeO— | — |
| 109 | H | CF 3 S— | H | H | H | MeO— | — |
| 110 | H | CF 3 S(O)— | H | H | H | MeO— | — |
| 111 | H | CF 3 S(O) 2 — | H | H | H | MeO— | |
| 112 | H | H | H | H | MeNHS(O) 2 — | MeO— | 186.5° C. |
| (decomp.) | |||||||
| 113 | H | H | H | H | (4-MePh)CH 2 NHS(O) 2 — | MeO— | 109.5° C. |
| (decomp.) | |||||||
| 114 | H | H | H | H | (3-ClPH)CH 2 NHS(O) 2 — | MeO— | * |
| 115 | H | H | H | H | [(2-pyridinylmethyl) | MeO— | 146.2° C. |
| amino]sulfonyl- | (decomp.) | ||||||
| 116 | H | H | H | H | (4-MePh)NHS(O) 2 — | MeO— | 161.2° C. |
| (decomp.) | |||||||
| 117 | H | SF 5 | H | H | H | MeO— | — |
| 118 | Cl | Cl | H | H | H | MeO— | — |
| 119 | Cl | H | H | H | NH 2 | MeO— | * |
| 120 | H | H | [{1-(difluoromethyl)- | H | Cl | MeO— | 227.4° C. |
| 1H-pyrazol-3-yl-} | (decomp.) | ||||||
| carbonyl]amino- | |||||||
| 121 | H | NO 2 | H | H | OH | MeO— | * |
| 122 | H | CF 3 | H | Cl | H | MeO— | — |
| 123 | H | CF 3 | H | H | Cl | MeO— | — |
| present | Melting | ||||||
| invention | R 1 | R 2 | R 3 | R 4 | R 5 | W | point |
| 124 | H | CF 3 | H | H | Me | MeO— | — |
| 125 | H | CF 3 | H | H | CF 3 | MeO— | — |
| 126 | H | CF 3 | H | H | OH | MeO— | — |
| 127 | H | CF 3 | H | H | MeO— | MeO— | — |
| 128 | H | CF 3 | H | H | EtO— | MeO— | — |
| 129 | H | CF 3 | H | H | iPrO— | MeO— | — |
| 130 | H | CF 3 | H | H | H 2 C═CHCH 2 O— | MeO— | — |
| 131 | H | CF 3 | H | H | MeC(O)O— | MeO— | — |
| 132 | H | CF 3 | H | H | BnO— | MeO— | — |
| 133 | H | CF 3 | H | H | NH 2 | MeO— | — |
| 134 | H | CF 3 | H | H | MeNH— | MeO— | — |
| 135 | H | CF 3 | H | H | Me 2 N— | MeO— | — |
| 136 | H | CF 3 | H | H | HC(O)NH— | MeO— | — |
| 137 | H | CF 3 | H | H | MeC(O)NH— | MeO— | — |
| 138 | H | CF 3 | H | H | CF 3 C(O)NH— | MeO— | — |
| 139 | H | C 3 F 7 | H | H | C 3 F 7 | MeO— | — |
| 140 | H | H | CF 3 | H | NH 2 | MeO— | 125.3° C. |
| 141 | H | (2-ClPh) | H | H | MeO— | MeO— | 235.3° C. |
| NHC(O)NH— | (decomp.) | ||||||
| 142 | CF 3 | H | H | H | H | EtO— | 50.8° C. |
| 144 | H | CF 3 | H | H | H | nPrO— | — |
| 145 | H | CF 3 | H | H | H | iPrO— | — |
| 146 | H | CF 3 | H | H | H | nBuO— | — |
| 147 | H | CF 3 | H | H | H | nC 5 H 11 O— | — |
| 148 | H | CF 3 | H | H | H | HC≡CCH 2 O— | — |
| 149 | H | CF 3 | H | H | H | HOCH 2 CH 2 O— | — |
| 150 | H | CF 3 | H | H | H | BnO— | — |
| invention | R 1 | R 2 | R 3 | R 4 | R 5 | W |
| 151 | H | CF 3 | H | H | H | (4-ClBn)O— |
| 152 | H | CF 3 | H | H | H | MeOC(O)CH 2 O— |
| 153 | H | CF 3 | H | H | H | Me 2 C=NO— |
| 154 | H | CF 3 | H | H | H | NH 2 |
| 155 | H | CF 3 | H | H | H | MeNH— |
| 156 | H | CF 3 | H | H | H | (NC)NH— |
| 157 | H | CF 3 | H | H | H | PhNH— |
| 158 | H | CF 3 | H | H | H | (3-Cl-4-MePh)NH— |
| 159 | H | CF 3 | H | H | H | (2,4-diMeOPh)NH— |
| 160 | H | CF 3 | H | H | H | HCNH— |
| 161 | H | CF 3 | H | H | H | NH 2 NH— |
| 162 | H | CF 3 | H | H | H | MeS— |
| 163 | H | CF 3 | H | H | H | MeOC(O)CH 2 S— |
| Test compound | root (%-untreated control plot) |
|---|---|
| Present Compound 3 | >5 |
| Present Compound 9 | >5 |
| Present Compound 11 | >5 |
| Present Compound 14 | >5 |
| Present Compound 15 | >5 |
| Present Compound 20 | >5 |
| Present Compound 22 | >5 |
| Present Compound 23 | >5 |
| Present Compound 26 | >5 |
| Present Compound 27 | >5 |
| Present Compound 29 | >5 |
| Present Compound 30 | >5 |
| Present Compound 31 | >5 |
| Present Compound 34 | >5 |
| Present Compound 35 | >5 |
| Present Compound 37 | >5 |
| Present Compound 38 | >5 |
| Present Compound 40 | >5 |
| Present Compound 41 | >5 |
| Present Compound 42 | >5 |
| Present Compound 43 | >5 |
| Present Compound 45 | >5 |
| Present Compound 47 | >5 |
| Present Compound 49 | >5 |
| Present Compound 50 | >5 |
| Present Compound 52 | >5 |
| Present Comoound 54 | >5 |
| Present Compound 55 | >5 |
| Present Compound 56 | >5 |
| Present Compound 58 | >5 |
| Present Compound 60 | >5 |
| Present Compound 61 | >5 |
| Present Compound 63 | >5 |
| Present Compound 64 | >5 |
| Present Compound 65 | >5 |
| Test compound | root (%-untreated control plot) |
|---|---|
| Present Compound 66 | >5 |
| Present Compound 67 | >5 |
| Present Compound 68 | >5 |
| Present Compound 69 | >5 |
| Present Compound 71 | >5 |
| Present Compound 74 | >5 |
| Present Compound 77 | >5 |
| Present Compound 79 | >5 |
| Present Compound 80 | >5 |
| Present Compound 82 | >5 |
| Present Compound 87 | >5 |
| Present Compound 88 | >5 |
| Present Compound 95 | >5 |
| Present Compound 96 | >5 |
| Present Compound 97 | >5 |
| Present Compound 100 | >5 |
| Present Compound 102 | >5 |
| Present Compound 103 | >5 |
| Present Compound 104 | >5 |
| Present Compound 106 | >5 |
| Present Compound 108 | >5 |
| Present Compound 109 | >5 |
| Test compound | root (%-untreated control plot) |
|---|---|
| Present Compound 114 | >5 |
| Present Compound 120 | >5 |
| Present Compound 121 | >5 |
| Present Compound 122 | >5 |
| Present Compound 123 | >5 |
| Present Compound 124 | >5 |
| Present Compound 126 | >5 |
| Present Compound 127 | >5 |
| Present Compound 128 | >5 |
| Present Compound 129 | >5 |
| Present Compound 131 | >5 |
| Present Compound 133 | >5 |
| Present Compound 136 | >5 |
| Present Compound 139 | >5 |
| Present Compound 140 | >5 |
| Present Compound 141 | >5 |
| Present Compound 142 | >5 |
| Present Compound 144 | >5 |
| Present Compound 145 | >5 |
| Present Compound 147 | >5 |
| Present Compound 148 | >5 |
| Present Compound 150 | >5 |
| Present Compound 153 | >5 |
| Present Compound 157 | >5 |
| Present Compound 159 | >5 |
| Present Compound 162 | >5 |
| Test compound | root (%-untreated control plot) |
|---|---|
| Present Compound 1 | >5 |
| Present Compound 4 | >5 |
| Present Compound 5 | >5 |
| Present Compound 7 | >5 |
| Present Compound 8 | >5 |
| Present Compound 10 | >5 |
| Present Compound 13 | >5 |
| Present Compound 16 | >5 |
| Present Compound 17 | >5 |
| Present Compound 18 | >5 |
| Present Compound 24 | >5 |
| Present Compound 25 | >5 |
| Present Compound 28 | >5 |
| Present Compound 32 | >5 |
| Present Compound 33 | >5 |
| Test compound | root (%-untreated control plot) |
|---|---|
| Present Compound 36 | >5 |
| Present Compound 44 | >5 |
| Present Compound 46 | >5 |
| Present Compound 48 | >5 |
| Present Compound 53 | >5 |
| Present Compound 75 | >5 |
| Present Compound 76 | >5 |
| Present Compound 78 | >5 |
| Present Compound 90 | >5 |
| Present Compound 91 | >5 |
| Present Compound 94 | >5 |
| Present Compound 98 | >5 |
| Present Compound 99 | >5 |
| Present Compound 101 | >5 |
| Present Compound 105 | >5 |
| Present Compound 111 | >5 |
| Present Compound 112 | >5 |
| Present Compound 130 | >5 |
| Present Compound 132 | >5 |
| Present Compound 134 | >5 |
| Present Compound 135 | >5 |
| Present Compound 138 | >5 |
| Present Compound 143 | >5 |
| Present Compound 146 | >5 |
| Present Compound 151 | >5 |
| Present Compound 152 | >5 |
| Present Compound 154 | >5 |
| Present Compound 155 | >5 |
| Present Compound 160 | >5 |
| Present Compound 161 | >5 |
| Present Compound 163 | >5 |
| Test compound | root (%-untreated control plot) |
|---|---|
| Present Compound 6 | >5 |
| Present Compound 12 | >5 |
| Present Compound 39 | >5 |
| Present Compound 51 | >5 |
| Present Compound 57 | >5 |
| Present Compound 59 | >5 |
| Present Compound 62 | >5 |
| Present Compound 73 | >5 |
| Present Compound 86 | >5 |
| Present Compound 89 | >5 |
| Present Compound 92 | >5 |
| Present Compound 107 | >5 |
| Present Compound 110 | >5 |
| Present Compound 113 | >5 |
| Present Compound 125 | >5 |
| Present Compound 137 | >5 |
| Present Compound 149 | >5 |
| Present Compound 156 | >5 |
| Test | Relative value of | |
|---|---|---|
| concentration | scores (%-untreated | |
| Test compound | (ppm) | control plot) |
| Present compound 1 | 10 | >5 |
| Present compound 3 | 0.3 | >5 |
| Present compound 7 | 10 | >5 |
| Present compound 10 | 10 | >5 |
| Present compound 12 | 10 | >5 |
| Present compound 13 | 10 | >5 |
| Present compound 19 | 0.3 | >5 |
| Present compound 26 | 1 | >5 |
| Present compound 27 | 10 | >5 |
| Present compound 30 | 10 | >5 |
| Present compound 32 | 3 | >5 |
| Present compound 38 | 3 | >5 |
| Present compound 39 | 1 | >5 |
| Present compound 40 | 10 | >5 |
| Present compound 41 | 0.3 | >5 |
| Present compound 42 | 0.3 | >5 |
| Present compound 43 | 3 | >5 |
| Present compound 48 | 10 | >5 |
| Present compound 49 | 10 | >5 |
| Present compound 52 | 1 | >5 |
| Test | Relative value of | |
|---|---|---|
| concentration | scores (%-untreated | |
| Test compound | (ppm) | control plot) |
| Present compound 55 | 10 | >5 |
| Present compound 56 | 10 | >5 |
| Present compound 57 | 10 | >5 |
| Present compound 58 | 10 | >5 |
| Present compound 60 | 10 | >5 |
| Present compound 62 | 0.3 | >5 |
| Present compound 63 | 3 | >5 |
| Present compound 65 | 0.3 | >5 |
| Present compound 67 | 3 | >5 |
| Present compound 69 | 1 | >5 |
| Present compound 70 | 10 | >5 |
| Present compound 73 | 1 | >5 |
| Present compound 83 | 0.3 | >5 |
| Present compound 85 | 10 | >5 |
| Present compound 88 | 3 | >5 |
| Present compound 93 | 10 | >5 |
| Present compound 97 | 0.3 | >5 |
| Present compound 100 | 3 | >5 |
| Present compound 110 | 1 | >5 |
| Present compound 111 | 10 | >5 |
| Test | Relative value of | |
|---|---|---|
| concentration | scores (%-untreated | |
| Test compound | (ppm) | control plot) |
| Present compound 119 | 1 | >5 |
| Present compound 125 | 0.3 | >5 |
| Present compound 129 | 10 | >5 |
| Present compound 130 | 1 | >5 |
| Present compound 131 | 3 | >5 |
| Present compound 132 | 0.3 | >5 |
| Present compound 133 | 3 | >5 |
| Present compound 135 | 3 | >5 |
| Present compound 141 | 0.3 | >5 |
| Present compound 145 | 0.3 | >5 |
| Present compound 147 | 0.3 | >5 |
| Present compound 152 | 1 | >5 |
| Present compound 153 | 1 | >5 |
| Present compound 156 | 1 | >5 |
| Present compound 157 | 0.3 | >5 |
| Present compound 159 | 0.3 | >5 |
| Present compound 160 | 10 | >5 |
| Present compound 161 | 3 | >5 |
Claims as granted
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12 codes- A01N43/56
- A01N47/32
- A01N43/54
- A01N47/04
- A01N43/12
- A01N47/06
- A01N43/36
- A01N43/40
- A01N43/80
- A01N47/02
- C07D409/04
- C07D333/70
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