6-membered heterocyclic derivatives and pharmaceutical composition comprising the same

The invention relates to a compound useful for the treatment of diseases or conditions associated with the P2X7 receptor and a pharmaceutical composition containing thereof.

Adenosine triphosphate (ATP) is known to serve as a source of energy in cells and a substrate of phosphorylation, as well as an extracellular messenger. It is known that ATP is released from a cell by various stimulation such as cellular injury, inflammation, nociceptive stimulus, reduced blood oxygen level, and also known to be released together with another messenger from a primary sensory nerve terminal. (Non-Patent Document 1) ATP thus released mediates various extracellular signal transductions through an ATP receptor.

ATP receptor is categorized into ionotropic P2X family and G protein-coupled P2Y family. For P2X family, seven subtypes have been reported, and a member of this family forms a homo-trimeric structure or a hetero-trimeric structure together with another member of this subtype and functions as a non-specific cation channel.

The P2X7 receptor, a non-selective cation channel, belongs to the P2X family, and forms a homo-trimeric structure. Activation of P2X7 by extracellular ATP allows for the passage of cations across the plasma membrane. Prolonged or repeated ATP stimulation leads to the pore formation of pannexin hemichannel, and induces the cellular activation following the release of small molecule such as ATP. (Non-Patent Document 2) It is reported that the activation of P2X7 is involved in inflammation, immune and pain by the maturation and secretion of proinflammatory cytokines such as interleukin-1 beta and interleukin-18. (Non-Patent Document 3) Thus, it is known that the P2X7 receptor is involved in pain, central nervous system disease, immune disease and inflammatory disease. (Non-Patent Document 7-8, and Patent Document 1)

P2X7 is distributed in macrophages, mast cells, microglia, and astrocytes. It is known that disruption of the P2X7 receptor gone abolishes chronic inflammatory and neuropathic pain. (Non-Patent Document 4) It is reported that the P451L mutation of the mouse P2X7 gene has impaired pore formation and shows less mechanical sensitivity of neuropathic pain model mice. (Non-Patent Document 5) Additionally, an association between lower pain intensity in chronic pain patients and the hypofunctional allele of P2X7 has been reported, suggesting that P2X7 antagonist is useful in the treatment of chronic pain such as rheumatoid arthritis, osteoarthritis and neuropathic pain.

Additionally, it has been reported that P2X7 may be involved in multiple sclerosis, spinal cord injury, stroke, Alzheimer's disease, and depression (Non-Patent Document 6), suggesting that P2X7 antagonist is useful in the treatment of these central nervous system disease.

The compounds having an analgesic effect are described in Patent Documents 2-5 and 8-11. However, the compounds have different chemical structures from the compounds of the present invention, and there is neither disclosure nor suggestion about an antagonistic activity for the P2X7 receptor.

The compounds having similar chemical structures to the compounds of the present invention and having an analgesic activity are described in Patent Documents 6, 7, and 12-15. However, there is neither disclosure nor suggestion about an antagonistic activity for the P2X7 receptor.

The compounds having an antagonistic activity for the P2X7 receptor are described in Patent Document 16. However, the compounds have different chemical structures from the compounds of the present invention.

Patent Document

[Patent Document 1] International Publication WO 2012/036193A

[Patent Document 2] International Publication WO 2014/200078A

[Patent Document 3] International Publication WO 2013/089212A

[Patent Document 4] International Publication WO 2012/020749A

[Patent Document 5] International Publication WO 2010/092966A

[Patent Document 6] International Publication WO 2013/118855A

[Patent Document 7] International Publication WO 2012/020742A

[Patent Document 8] US Publication No. 2011/0319418A

[Patent Document 9] International Publication WO 2006/104715A

[Patent Document 10] International Publication WO 2006/104713A

[Patent Document 11] International Publication WO 2006/102112A

[Patent Document 12] US Publication No. 2011/0319400A

[Patent Document 13] International Publication WO 2009/058653A

[Patent Document 14] International Publication WO 2007/079214A

[Patent Document 15] International Publication WO 2007/079163A

[Patent Document 16] International Publication WO 2015/099107A

Non-Patent Document

[Non-patent Document 1] Burnstock G., Mol Pain. 2009, 5, 69

[Non-patent Document 2] Baroja-Mazo A et al., Biochim Biophys Acta. 201.3, 1828, 79-93

[Non-patent Document 3] MacKenzie A et al., Immunity. 2001, 15, 825-835

[Non-patent Document 4] Chessell I P et al., Pain. 2005, 114, 386-396

[Non-patent Document 5] Sorge R E et al., Nature Med. 2012, 18, 595-599

[Non-patent Document 6] Skaper S D et al., FASER J. 2010, 24, 337-345

[Non-patent Document 7] Takenouchi T et al., Arch Immunol Ther Exp (Warsz). 2010 April; 58(2): 91-6

[Non-patent Document 8] Friedle S A et al., Recent Pat CNS Drug Discov. 2010 January; 5(1): 35-45

[Non-patent Document 9] Journal of Medicinal Chemistry 2010, 53(22), 7918-7931

Problems to be Solved by the Invention

The objective of the present invention is to provide novel compounds having an antagonistic activity for the P2X7 receptor and a pharmaceutical composition having an antagonistic activity for the P2X7 receptor.

Means for Solving the Problem

The present invention relates to the following (1), (1α), (1a′), (2) to (96) and (1001) to (1.007):

(1)

A compound represented by Formula (I):

wherein

Y 1 and Y 2 are each independently N(R Y ), O or S:

Z is C(R 4 ) or N; Z 2a is C(R 5a ) or N; Z 2b is C(R 5a )(R 5a′ ) or N(R 5b ); Z 2c is C(R 5a ) or N; Z 3a is C(R 6 ) or N;

provided that when Z 1 is N, then each of Z 2a , Z 2b and Z 2c is C(R 5a ):

when Z 1 is C(R 4 ), then Z 2e is N; and

when Z 2a is N, then Z 3a is C(R 6 );

R Y is each independently a hydrogen atom, hydroxy, cyano, carboxy, carbamoyl, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl; R 4 and R 6 are each independently a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, or substituted or unsubstituted alkynylamino; R 5a and R 5a′ are each independently a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfonyl, substituted or unsubstituted alkylcarbonyloxy, substituted or unsubstituted alkenylcarbonyloxy, substituted or unsubstituted alkynylcarbonyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylsulfonyloxy, substituted or unsubstituted alkenylsulfonyloxy, substituted or unsubstituted alkynylsulfonyloxy, substituted or unsubstituted alkyloxysulfonyl, substituted or unsubstituted alkenyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylsulfamoyl, substituted or unsubstituted alkenylsulfamoyl, substituted or unsubstituted alkynylsulfamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkylsulfonylamino, substituted or unsubstituted alkenylsulfonylamino, substituted or unsubstituted alkynylsulfonylamino, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted alkenyloxycarbonylamino, substituted or unsubstituted alkynyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylcarbonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic heterocyclylcarbonyloxy, substituted or unsubstituted non-aromatic hoterocyclylcarbonyloxy, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy, substituted or unsubstituted aromatic hetorocyclylsulfonyloxy, substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy, substituted or unsubstituted aromatic carbocyclyloxyaulfonyl, substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl, substituted or unsubstituted aromatic heterocyclyloxysulfonyl, substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic hetorocyclylcarbamoyl, substituted or unsubstituted non-aromatic hetorocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, substituted or unsubstituted non-aromatic heterocyclylsulfamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonylamino, substituted or unsubstituted aromatic heterocyclylcarbonylamino, substituted or unsubstituted non-aromatic heterocyclylcarbonylamino, substituted or unsubstituted aromatic carbocyclylsulfonylamino, substituted or unsubstituted non-aromatic carbocyclylsulfonylamino, substituted or unsubstituted aromatic hctorocyclylsulfonylamino, substituted or unsubstituted non-aromatic heterocyclylsulfonylamino, substituted or unsubstituted aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted aromatic hoterocyclyloxycarbonylamino, or substituted or unsubstituted non aromatic heterocyclyloxycarbonyl amino; R 5b is a hydrogen atom, carboxy, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarhonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic; carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, or substituted or unsubstituted non-aromatic heterocyclylcarbamoyl; R 1 is substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heLerocyclyl; R 2a is each independently a hydrogen atom, halogen, hydroxy, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy; R 2b is each independently a hydrogen atom, halogen, hydroxy, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy; R 2a and R 2b which are attached to the same carbon atom may be taken together to form oxo; X is N(R 7a ), C(R 8a )(R 8b ), O or S; R 7a is a hydrogen atom, substituted or unsubstituted alkyl, or substituted or unsubstituted alkylcarbonyl; R 8a and R 8b are each independently a hydrogen atom, halogen, hydroxy, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy; R 2c is each independently a hydrogen atom, halogen, hydroxy, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy; R 2d is each independently a hydrogen atom, halogen, hydroxy, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy; R 2c and R 2d which are attached to the same carbon atom may be taken together to form a substituted or unsubstituted non-aromatic carbocycle, or two R 2c may be taken together to form a substituted or unsubstituted non-aromatic carbocycle; R 3 is a group represented by the Formula:

wherein

Ring B is a 6-membered aromatic carbocycle, a 6-membered non-aromatic carbocycle, a 6-membered aromatic heterocycle, or a 6-membered non-aromatic heterocycle; Ring C is a 5-membered non-aromatic carbocycle, a 5-membered aromatic heterocycle, or a 5-membered non-aromatic heterocycle; Ring D is a 5-membered non-aromatic carbocycle, or a 6-membered non-aromatic carbocycle; R 9a and R 10a are each independently halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted or alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfonyl, substituted or unsubstituted alkylcarbonyloxy, substituted or unsubstituted alkenylcarbonyloxy, substituted or unsubstituted alkynylcarbonyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylsulfonyloxy, substituted or unsubstituted alkenylsulfonyloxy, substituted or unsubstituted alkynylsulfonyloxy, substituted or unsubstituted alkyloxysulfonyl, substituted or unsubstituted alkenyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylsulfamoyl, substituted or unsubstituted alkenylsulfamoyl, substituted or unsubstituted alkynylsulfamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkylsulfonylamino, substituted or unsubstituted alkenylsulfonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylcarbonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic heterocyclylcarbonyloxy, substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarhonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy, substituted or unsubstituted aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy, substituted or unsubstituted aromatic carbocyclyloxysulfonyl, substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl, substituted or unsubstituted aromatic heterocyclyloxysulfonyl, substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, substituted or unsubstituted non-aromatic heterocyclylsulfamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonylamino, substituted or unsubstituted aromatic heterocyclylcarbonylamino, substituted or unsubstituted non-aromatic heterocyclylcarbonylamino, substituted or unsubstituted aromatic carbocyclylsulfonylamino, substituted or unsubstituted non-aromatic carbocyclylsulfonylamino, substituted or unsubstituted aromatic heterocyclylsulfonylamino, substituted or unsubstituted non-aromatic heterocyclylsulfonylamino, substituted or unsubstituted aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted aromatic heterocyclyloxycarbonylamino, or substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino; R 10a , R 10b , R 10c and R 10d are each independently halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfonyl, substituted or unsubstituted alkylcarbonyloxy, substituted or unsubstituted alkenylcarbonyloxy, substituted or unsubstituted alkynylcarbonyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylsulfonyloxy, substituted or unsubstituted alkenylsulfonyloxy, substituted or unsubstituted alkynylsulfonyloxy, substituted or unsubstituted alkyloxysulfonyl, substituted or unsubstituted alkenyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylsulfamoyl, substituted or unsubstituted alkenylsulfamoyl, substituted or unsubstituted alkynylsulfamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkylsulfonylamino, substituted or unsubstituted alkenylsulfonylamino, substituted or unsubstituted alkynylsulfonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylcarbonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic heterocyclylcarbonyloxy, substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy, substituted or unsubstituted aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic hetorocyclylsulfonyloxy, substituted or unsubstituted aromatic carbocyclyloxysulfonyl, substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl, substituted or unsubstituted aromatic heterocyclyloxysulfonyl, substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, substituted or unsubstituted non-aromatic heterocyclylsulfamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonylamino, substituted or unsubstituted aromatic heterocyclylcarbonylamino, substituted or unsubstituted non-aromatic heterocyclylcarbonylamino, substituted or unsubstituted aromatic carbocyclylsulfonylamino, substituted or unsubstituted non-aromatic carbocyclylsulfonylamino, substituted or unsubstituted aromatic heterocyclylsulfonylamino, substituted or unsubstituted non-aromatic heterocyclylsulfonylamino, substituted or unsubstituted aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted aromatic hoterocyclyloxycarbonylamino, or substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino; R 9a , R 9b , R 10a and R 10b may be any of the following a) to c): a) R 9a and R 10a , or R 9b and R 10b are taken together to form a (C1-C3) bridge, wherein one of the carbon atoms constituting the bridge may be replaced with an oxygen atom or a nitrogen atom; b) R 9a and R 10a which are attached to the adjacent atoms, or R 9b and R 10b which are attached to the adjacent atoms are taken together to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle; and c) two R 10a which are attached to the adjacent atom, or two R 10b which are attached to the adjacent atom are taken together to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle; and

R 10e is each independently halogen, hydroxy, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy; n is an integer from 1 to 5; m is an integer from 0 to 4; p1 is an integer from 0 to 3; p2 is an integer from 0 to 2; p3 is an integer from 0 to 2;

provided that

i) when X is C(R 7a )(R 7b ), O or S and one of R 5a and R 5b′ is hydrogen, then the other of R 5a and R 5a′ is not a hydrogen atom, hydroxy, methyl substituted with a substituted or unsubstituted 6-membered cyclic group, octadecyloxy, or ethyloxycarbonyl, i′) when X is C(R 7a )(R 7b ), O or S, then R 5b is not a hydrogen atom or methyl substituted with a substituted or unsubstituted 6-membered cyclic group; and ii) when X is O, n is 1, and

then R 2a and R 2b are not taken together to form oxo,

provided that the following compounds are excluded:

or a pharmaceutically acceptable salt thereof.

The above definition of R 3 moans that R 10e is a substituent on Ring D, R 10c is a substituent on Ring B, and R 10d is a substituent on Ring C.

(1α)

The compound according to the above (1), wherein

Y 1 and Y 2 are each independently O or S; and Z 2b is CH(R 5a ) or N(R 5b ).

or a pharmaceutically acceptable salt thereof.

(1α′)

A compound represented by Formula (I):

wherein

Y 1 and Y 2 are each independently O or S;

Z 1 is C(R 4 ) or N;

Z 2a is C(R 5a ) or N;

Z 2b is CH(R 5a ) or N(R 5b );

Z 2c is C(R 5a ) or N;

Z 3a is C(R 5 ) or N;

provided that when Z 1 is N, then each of Z 2a , Z 2b and Z 2c is C(R 5a );

when Z 1 is C(R 4 ), then Z 2c is N; and

when Z 2a is N, then Z 8a is C(R 6 ):

R 4 and R 6 are each independently a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkonylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, or substituted or unsubstituted alkynylamino; R 5a is a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfonyl, substituted or unsubstituted alkylcarbonyloxy, substituted or unsubstituted alkenylcarbonyloxy, substituted or unsubstituted alkynylcarbonyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylsulfonyloxy, substituted or unsubstituted alkenylsulfonyloxy, substituted or unsubstituted alkynylsulfonyloxy, substituted or unsubstituted alkyloxysulfonyl, substituted or unsubstituted alkonyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylsulfamoyl, substituted or unsubstituted alkenylsulfamoyl, substituted or unsubstituted alkynylsulfamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenyl carbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkylsulfonylamino, substituted or unsubstituted alkenylsulfonylamino, substituted or unsubstituted alkynylsulfonylamino, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted alkenyloxycarbonylamino, substituted or unsubstituted alkynyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylcarbonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic heterocyclylcarbonyloxy, substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy, substituted or unsubstituted aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy, substituted or unsubstituted aromatic carbocyclyloxysulfonyl, substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl, substituted or unsubstituted aromatic heterocyclyloxysulfonyl, substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, substituted or unsubstituted non-aromatic heterocyclylsulfamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonylamino, substituted or unsubstituted aromatic heterocyclylcarbonylamino, substituted or unsubstituted non-aromatic heterocyclylcarbonylamino, substituted or unsubstituted aromatic carbocyclylsulfonylamino, substituted or unsubstituted non-aromatic carbocyclylsulfonylamino, substituted or unsubstituted aromatic heterocyclylsulfonylamino, substituted or unsubstituted non-aromatic heterocyclylsulfonylamino, substituted or unsubstituted aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted aromatic heterocyclyloxycarbonylamino, or substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino; R 5b is a hydrogen atom, carboxy, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic hetorocyclylcarbamoyl, or substituted or unsubstituted non-aromatic heterocyclylcarbamoyl; R 1 is substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl; R 2a is each independently a hydrogen atom, halogen, hydroxy, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy; R 2b is each independently a hydrogen atom, halogen, hydroxy, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy; R 2a and R 2b which are attached to the same carbon atom may be taken together to form oxo; X is N(R 7a ), C(R 8a )(R 8b ), O or S; R 7a is a hydrogen atom, substituted or unsubstituted alkyl, or substituted or unsubstituted alkylcarbonyl; R 8a and R 8b are each independently a hydrogen atom, halogen, hydroxy, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy; R 2c is each independently a hydrogen atom, halogen, hydroxy, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy; R 2d is each independently a hydrogen atom, halogen, hydroxy, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy; R 2c and R 2d which are attached to the same carbon atom may be taken together to form a substituted or unsubstituted non-aromatic carbocycle, or two R 2c may be taken together to form a substituted or unsubstituted non-aromatic carbocycle; R 3 is a group represented by the Formula:

wherein

Ring R is a 6-membered aromatic carbocycle, a 6-membered non-aromatic carbocycle, a 6-membered aromatic heterocycle, or a 6-membered non-aromatic heterocycle; Ring C is a 5-membered non-aromatic carbocycle, a 5-membered aromatic heterocycle, or a 5-membered non-aromatic heterocycle; Ring D is a 5-membered non-aromatic carbocycle, or a 6-membered non-aromatic carbocycle; R 9a and R 9b are each independently halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfonyl, substituted or unsubstituted alkylcarbonyloxy, substituted or unsubstituted alkenylcarbonyloxy, substituted or unsubstituted alkynylcarbonyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylsulfonyloxy, substituted or unsubstituted alkenylsulfonyloxy, substituted or unsubstituted alkynylsulfonyloxy, substituted or unsubstituted alkyloxysulfonyl, substituted or unsubstituted alkenyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylsulfamoyl, substituted or unsubstituted alkenylsulfamoyl, substituted or unsubstituted alkynylsulfamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkylsulfonylamino, substituted or unsubstituted alkenylsulfonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylcarbonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic heterocyclylcarbonyloxy, substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy, substituted or unsubstituted aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy, substituted or unsubstituted aromatic carbocyclyloxysulfonyl, substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl, substituted or unsubstituted aromatic heterocyclyloxysulfonyl, substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, substituted or unsubstituted non-aromatic heterocyclylsulfamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonylamino, substituted or unsubstituted aromatic heterocyclylcarbonylamino, substituted or unsubstituted non-aromatic heterocyclylcarbonylamino, substituted or unsubstituted aromatic carbocyclylsulfonylamino, substituted or unsubstituted non-aromatic carbocyclylsulfonylamino, substituted or unsubstituted aromatic heterocyclylsulfonylamino, substituted or unsubstituted non-aromatic heterocyclylsulfonylamino, substituted or unsubstituted aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted aromatic heterocyclyloxycarbonylamino, or substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino; R 10a , R 10b , R 10c and R 10d are each independently halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfonyl, substituted or unsubstituted alkylcarbonyloxy, substituted or unsubstituted alkenylcarbonyloxy, substituted or unsubstituted alkynylcarbonyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylsulfonyloxy, substituted or unsubstituted alkenylsulfonyloxy, substituted or unsubstituted alkynylsulfonyloxy, substituted or unsubstituted alkyloxysulfonyl, substituted or unsubstituted alkenyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylsulfamoyl, substituted or unsubstituted alkenylsulfamoyl, substituted or unsubstituted alkynylsulfamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkylsulfonylamino, substituted or unsubstituted alkenylsulfonylamino, substituted or unsubstituted alkynylsulfonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylcarbonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic heterocyclylcarbonyloxy, substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy, substituted or unsubstituted aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy, substituted or unsubstituted aromatic carbocyclyloxysulfonyl, substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl, substituted or unsubstituted aromatic heterocyclyloxysulfonyl, substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, substituted or unsubstituted non-aromatic heterocyclylsulfamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonylamino, substituted or unsubstituted aromatic heterocyclylcarbonylamino, substituted or unsubstituted non-aromatic heterocyclylcarbonylamino, substituted or unsubstituted aromatic carbocyclylsulfonylamino, substituted or unsubstituted non-aromatic carbocyclylsulfonylamino, substituted or unsubstituted aromatic heterocyclylsulfonylamino, substituted or unsubstituted non-aromatic heterocyclylsulfonylamino, substituted or unsubstituted aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted aromatic heterocyclyloxycarbonylamino, or substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino; R 9a , R 9b , R 10a and R 10b may be any of the following a) to c): a) R 9a and R 10a , or R 9b and R 10b are taken together to form a (C1-C3) bridge, wherein one of the carbon atoms constituting the bridge may be replaced with an oxygen atom or a nitrogen atom; b) R 9a and R 10a which are attached to the adjacent atoms, or R 9b and R 10b which are attached to the adjacent atoms are taken together to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle; and c) two R 10a which are attached to the adjacent atom, or two R 10b which are attached to the adjacent atom are taken together to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle; and

R 10e is each independently halogen, hydroxy, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy; n is an integer from 1 to 5; m is an integer from 0 to 4; p1 is an integer from 0 to 3; p2 is an integer from 0 to 2; p3 is an integer from 0 to 2;

provided that

i) when X is C(R 7a )(R 7b ). O or S, then R 5a is not a hydrogen atom, hydroxy, methyl substituted with a substituted or unsubstituted G-membered cyclic group, octadecyloxy, or ethyloxycarbonyl, and i′) when X is C(R 7a )(R 7b ), O or S, then R 5b is not a hydrogen atom or methyl substituted with a substituted or unsubstituted 6-membered cyclic group; and ii) when X is O, n is 1, and

then R 2a and R 2b are not taken together to form oxo,

provided that the following compounds are excluded:

or a pharmaceutically acceptable salt thereof.

(2)

The compound according to the above (1), (1α), or (1α′), wherein

X is N(R 7a ) or O.

or a pharmaceutically acceptable salt thereof.

(3)

The compound according to the above (0.1), (1α) or (1α′), wherein

X is N(R 7a ),

or a pharmaceutically acceptable salt thereof.

(4)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (3), wherein

R 7a is a hydrogen atom or substituted or unsubstituted alkyl,

or a pharmaceutically acceptable salt thereof.

(5)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (3), wherein

R 7a is a hydrogen atom,

or a pharmaceutically acceptable salt thereof.

(6)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (5), wherein

or a pharmaceutically acceptable salt thereof.

(7)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (5), wherein

or a pharmaceutically acceptable salt thereof.

(8)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (5), wherein

or a pharmaceutically acceptable salt thereof.

(9)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (5), wherein

is

or a pharmaceutically acceptable salt thereof.

(10)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (9), wherein

R 1 is substituted or unsubstituted 6- to 10-membered aromatic carbocyclyl, substituted or unsubstituted 3- to 10-membered non-aromatic carbocyclyl, substituted or unsubstituted 5- to 10-membered aromatic heterocyclyl, or substituted or unsubstituted 3- to 10-membered non-aromatic heterocyclyl,

or a pharmaceutically acceptable salt thereof.

(11)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (9), wherein

R 1 is substituted or unsubstituted 6-membered aromatic carbocyclyl, substituted or unsubstituted 3- to 6-membered non-aromatic carbocyclyl, substituted or unsubstituted 5- to 6-membered aromatic heterocyclyl, or substituted or unsubstituted 5- to 6-membered non-aromatic heterocyclyl,

or a pharmaceutically acceptable salt thereof.

(12)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (9), wherein

R 1 is substituted or unsubstituted 6-membered aromatic carbocyclyl, or substituted or unsubstituted 5- to 6-membered aromatic heterocyclyl,

or a pharmaceutically acceptable salt thereof.

(13)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (9), wherein

R 1 is 6-membered aromatic carbocyclyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s), 3- to 6-membered non-aromatic carbocyclyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s), 5- to 6-membered aromatic heterocyclyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s), or 5- to 6-membered non-aromatic heterocyclyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s),

or a pharmaceutically acceptable salt thereof.

(14)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (9), wherein

R 1 is 6-membered aromatic carbocyclyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s), or 5- to 6-membered aromatic heterocyclyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different, substituent(s),

or a pharmaceutically acceptable salt thereof.

(15)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (9), wherein

R 3 is

or a pharmaceutically acceptable salt thereof.

(16)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (15), wherein

R 9a and R 9b are each independently halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfinyl, substituted or unsubstituted alkylcarbonyloxy, substituted or unsubstituted alkenylcarbonyloxy, substituted or unsubstituted alkynylcarbonyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylsulfonyloxy, substituted or unsubstituted alkenylsulfonyloxy, substituted or unsubstituted alkynylsulfonyloxy, substituted or unsubstituted aryloxysulfonyl, substituted or unsubstituted alkenyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylsulfamoyl, substituted or unsubstituted alkenylsulfamoyl, substituted or unsubstituted alkynylsulfamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkylsulfonylamino, substituted or unsubstituted alkenylsulfonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylcarbonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic heterocyclylcarbonyloxy, substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy, substituted or unsubstituted aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy, substituted or unsubstituted aromatic carbocyclyloxysulfonyl, substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl, substituted or unsubstituted aromatic heterocyclyloxysulfonyl, substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, substituted or unsubstituted non-aromatic heterocyclylsulfamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonylamino, substituted or unsubstituted aromatic heterocyclylcarbonylamino, substituted or unsubstituted non-aromatic heterocyclylcarbonylamino, substituted or unsubstituted aromatic carbocyclylsulfonylamino, substituted or unsubstituted non-aromatic carbocyclylsulfonylamino, substituted or unsubstituted aromatic heterocyclylsulfonylamino, substituted or unsubstituted non-aromatic heterocyclylsulfonylamino, substituted or unsubstituted aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted aromatic heterocyclyloxycarbonylamino, or substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino

or a pharmaceutically acceptable salt, thereof.

(17)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (15), wherein

R 9a and R 9b are each independently halogen, hydroxy, amino, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfinyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy,

or a pharmaceutically acceptable salt thereof.

(18)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (15), wherein

R 9a and R 9b are each independently halogen, hydroxy, amino, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy,

or a pharmaceutically acceptable salt thereof.

(19)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (15), wherein

R 9a and R 9b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkonyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, or substituted or unsubstituted alkynylsulfanyl,

or a pharmaceutically acceptable salt thereof.

(20)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (15), wherein

R 9a and R 9b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, or substituted or unsubstituted alkynyl,

or a pharmaceutically acceptable salt thereof.

(21)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (15), wherein

R 9a and R 9b are each independently substituted or unsubstituted alkyl,

or a pharmaceutically acceptable salt thereof.

(22)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (21), wherein

R 10a and R 10b are each independently halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfinyl, substituted or unsubstituted alkylcarbonyloxy, substituted or unsubstituted alkenylcarbonyloxy, substituted or unsubstituted alkynylcarbonyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylsulfonyloxy, substituted or unsubstituted alkenylsulfonyloxy, substituted or unsubstituted alkynylsulfonyloxy, substituted or unsubstituted aryloxysulfonyl, substituted or unsubstituted alkenyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylsulfamoyl, substituted or unsubstituted alkenylsulfamoyl, substituted or unsubstituted alkynylsulfamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynyl carbonyl amino, substituted or unsubstituted alkylsulfonylamino, substituted or unsubstituted alkenylsulfonylamino, substituted or unsubstituted alkynylsulfonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclyl amino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylcarbonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic heterocyclylcarbonyloxy, substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy, substituted or unsubstituted aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy, substituted or unsubstituted aromatic carbocyclyloxysulfonyl, substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl, substituted or unsubstituted aromatic heterocyclyloxysulfonyl, substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, substituted or unsubstituted non-aromatic heterocyclylsulfamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonylamino, substituted or unsubstituted aromatic heterocyclylcarbonyl amino, substituted or unsubstituted non-aromatic, heterocyclylcarbonylamino, substituted or unsubstituted aromatic carbocyclylsulfonylamino, substituted or unsubstituted non-aromatic carbocyclylsulfonylamino, substituted or unsubstituted aromatic heterocyclylsulfonylamino, substituted or unsubstituted non-aromatic heterocyclylsulfonylamino, substituted or unsubstituted aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted aromatic heterocyclyloxycarbonylamino, or substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino,

or a pharmaceutically acceptable salt thereof.

(23)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (21), wherein

R 10a and R 10b are each independently halogen, hydroxy, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynyl sulfonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, or substituted or unsubstituted non-aromatic heterocyclylsulfamoyl,

or a pharmaceutically acceptable salt, thereof.

(24)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (21), wherein

R 10a and R 10b are each independently halogen, hydroxy, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, or substituted or unsubstituted non-aromatic heterocyclylsulfamoyl,

or a pharmaceutically acceptable salt thereof.

(25)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (21), wherein

R 10a and R 10b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy,

or a pharmaceutically acceptable salt thereof.

(26)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (21), wherein

R 10a and R 10b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy,

or a pharmaceutically acceptable salt thereof.

(27)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (26), wherein

p1 is 1 or 2,

or a pharmaceutically acceptable salt thereof.

(28)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (27), wherein

p2 is 1.

or a pharmaceutically acceptable salt thereof.

(29)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (28), wherein

R 3 is

or a pharmaceutically acceptable salt thereof.

(30)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (29), wherein

R 10c and R 10d are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy,

or a pharmaceutically acceptable salt thereof.

(31)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (29), wherein

R 10c and R 10d are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy,

or a pharmaceutically acceptable salt thereof.

(32)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (29), wherein

R 10c and R 10d are each independently halogen, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy,

or a pharmaceutically acceptable salt thereof.

(33)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (32), wherein

R 10c is each independently halogen, or substituted or unsubstituted alkyl,

or a pharmaceutically acceptable salt thereof.

(34)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (33), wherein

p3 is 0,

or a pharmaceutically acceptable salt thereof.

(35)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (28), wherein

R 3 is a group represented by the formula:

wherein

R 11a and R 11b are each independently halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfonyl, substituted or unsubstituted alkylcarbonyloxy, substituted or unsubstituted alkenylcarbonyloxy, substituted or unsubstituted alkynylcarbonyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxy carbonyl, substituted or unsubstituted alkylsulfonyloxy, substituted or unsubstituted alkenylsulfonyloxy, substituted or unsubstituted alkynylsulfonyloxy, substituted or unsubstituted aryloxysulfonyl, substituted or unsubstituted alkenyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylsulfamoyl, substituted or unsubstituted alkenylsulfamoyl, substituted or unsubstituted alkynylsulfamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkylsulfonylamino, substituted or unsubstituted alkenylsulfonylamino, substituted or unsubstituted alkynylsulfonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic, heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylcarbonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic heterocyclylcarbonyloxy, substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclyl sulfon yloxy, substituted or unsubstituted aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic heterocyclyl sulfonyloxy, substituted or unsubstituted aromatic carbocyclyloxysulfonyl, substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl, substituted or unsubstituted aromatic heterocyclyloxysulfonyl, substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic, heterocyclylsulfamoyl, substituted or unsubstituted non-aromatic heterocyclylsulfamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonylamino, substituted or unsubstituted aromatic heterocyclylcarbonylamino, substituted or unsubstituted non-aromatic heterocyclylcarbonyl amino, substituted or unsubstituted aromatic carbocyclylsulfonylamino, substituted or unsubstituted non-aromatic carbocyclylsulfonylamino, substituted or unsubstituted aromatic heterocyclylsulfonylamino, substituted or unsubstituted non-aromatic heterocyclylsulfonylamino, substituted or unsubstituted aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted aromatic heterocyclyloxycarbonylamino, or substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino.

R 11c

is taken together with R 9a which is attached to the adjacent atom to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle;

is taken together with R 11a which is attached to the adjacent atom to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle; or

is taken together with R 11a which is attached to a non-adjacent atom to form a (C1-C3) bridge, wherein one of the carbon atoms constituting the bridge may be replaced with an oxygen atom or a nitrogen atom:

R 11d

it taken together with R 9b which is attached to the adjacent atom to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle;

is taken together with R 11b which is attached to the adjacent atom to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle; or

is taken together with R 11b which is attached to a non-adjacent atom to form a (C1-C3) bridge, wherein one of the carbon atoms constituting the bridge may be replaced with an oxygen atom or a nitrogen atom;

p1a is an integer from 0 to 2; and

p2a is 0 or 1,

or a pharmaceutically acceptable salt thereof.

(36)

The compound according to the above (35), wherein

R 11c is taken together with R 9b which is attached to the adjacent atom to form a substituted or unsubstituted 5- to 6-membered non-aromatic carbocycle, a substituted or unsubstituted 5- to 6-membered aromatic heterocycle, or a substituted or unsubstituted 5- to 6-membered non-aromatic heterocycle,

or a pharmaceutically acceptable salt thereof.

(37)

The compound according to the above (35), wherein

R 11d is token together with R 9b which is attached to the adjacent atom to form a substituted or unsubstituted 6-membered aromatic carbocycle, or a substituted or unsubstituted 6-membered aromatic heterocycle,

or a pharmaceutically acceptable salt thereof.

(38)

The compound according to the above (35), wherein

R 11c is taken together with R 11a which is attached to the adjacent atom to form a substituted or unsubstituted 5- to 6-membered non-aromatic carbocycle, a substituted or unsubstituted 5- to 6-membered aromatic heterocycle, or a substituted or unsubstituted 5- to 6-membered non-aromatic heterocycle,

or a pharmaceutically acceptable salt thereof.

(39)

The compound according to the above (35), wherein

R 11d is taken together with R 11b which is attached to the adjacent atom to form a substituted or unsubstituted 6-membered aromatic carbocycle, or a substituted or unsubstituted 6-membered aromatic heterocycle,

or a pharmaceutically acceptable salt thereof.

(40)

The compound according to the above (35), wherein

Ring B is a 6-membered non-aromatic carbocycle, or a 6-membered non-aromatic heterocycle; and

R 11c is taken together with R 11a which is attached to a non-adjacent atom to form a (C1-C3) bridge consisting of carbon,

or a pharmaceutically acceptable salt thereof.

(41)

The compound according to the above (35), wherein

Ring C is a 5-membered non-aromatic carbocycle, or a 5-membered non-aromatic heterocycle; and

R 11d is taken together with R 11b which is attached to a nonadjacent atom to form a (C1-C3) bridge consisting of carbon,

or a pharmaceutically acceptable salt thereof.

(42)

The compound according to any one of the above (35) to (41), wherein

R 11a and R 11b are each independently halogen, hydroxy, amino, carbamoyl, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, or substituted or unsubstituted alkynylamino,

or a pharmaceutically acceptable salt thereof.

(43)

The compound according to any one of the above (35) to (41), wherein

R 11a and R 11b are each independently halogen, hydroxy, amino, carbamoyl, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, or substituted or unsubstituted alkynyloxy,

or a pharmaceutically acceptable salt thereof.

(41)

The compound according to any one of the above (35) to (41), wherein

R 11a and R 11b are each independently halogen, or substituted or unsubstituted alkyl,

or a pharmaceutically acceptable salt thereof.

(45)

The compound according to any one of the above (35) to (44), wherein

p1a is 0 or 1,

or a pharmaceutically acceptable salt thereof.

(46)

The compound according to any one of the above (35) to (45), wherein

p2a is 0,

or a pharmaceutically acceptable salt thereof.

(47)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (46), wherein

Ring B is a 6-membered aromatic carbocycle or a 6-membered aromatic heterocycle,

or a pharmaceutically acceptable salt thereof.

(48)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (46), wherein

Ring C is a 5-membered aromatic heterocycle,

or a pharmaceutically acceptable salt thereof.

(49)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (48), wherein

R 5a is a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenyl sulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted alkenyloxycarbonylamino, substituted or unsubstituted alkynyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl,

or a pharmaceutically acceptable salt thereof.

(50)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (48), wherein

R 5a is a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl.

or a pharmaceutically acceptable salt thereof.

(51)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (48), wherein

R 5a is a hydrogen atom, halogen, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl,

or a pharmaceutically acceptable salt thereof.

(52)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (48), wherein

R 5a is a hydrogen atom, halogen, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy,

or a pharmaceutically acceptable salt thereof.

(53)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (52), wherein

R 5b is a hydrogen atom, carboxy, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl,

or a pharmaceutically acceptable salt thereof.

(54)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (52), wherein

R 5b is a hydrogen atom, or substituted or unsubstituted alkyl,

or a pharmaceutically acceptable salt, thereof.

(55)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (52), wherein

R 5b is substituted or unsubstituted alkyl,

or a pharmaceutically acceptable salt thereof.

(56)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (55), wherein

n is an integer from 1 to 3,

or a pharmaceutically acceptable salt thereof.

(57)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (55), wherein

n is 1.

or a pharmaceutically acceptable salt thereof.

(58)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (57), wherein

R 3a is each independently a hydrogen atom, halogen, or substituted or unsubstituted alkyl, or R 2a and R 2b which are attached to the same carbon atom are taken together to form oxo,

or a pharmaceutically acceptable salt thereof.

(59)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (57), wherein

R 2a is each independently a hydrogen atom, halogen, or substituted or unsubstituted alkyl,

or a pharmaceutically acceptable salt thereof.

(60)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (57), wherein

R 2a in a hydrogen atom,

or a pharmaceutically acceptable salt thereof.

(61)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (60), wherein

R 2b is each independently a hydrogen atom, halogen, or substituted or unsubstituted alkyl, or R 2a and R 2b which are attached to the same carbon atom are taken together to form oxo,

or a pharmaceutically acceptable salt thereof.

(62)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (60), wherein

R 2b is each independently a hydrogen atom, halogen, or substituted or unsubstituted alkyl,

or a pharmaceutically acceptable salt thereof.

(63)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (60), wherein

R 2b is a hydrogen atom,

or a pharmaceutically acceptable salt, thereof.

(64)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (63), wherein

m is an integer from 0 to 2,

or a pharmaceutically acceptable salt thereof.

(65)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (63), wherein

m is 0,

or a pharmaceutically acceptable salt thereof.

(66)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (65), wherein

R 2c is each independently a hydrogen atom, halogen, or substituted or unsubstituted alkyl,

or a pharmaceutically acceptable salt thereof.

(67)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (65), wherein

R 2c is a hydrogen atom,

or a pharmaceutically acceptable salt thereof.

(68)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (67), wherein

R 2d is each independently a hydrogen atom, halogen, or substituted or unsubstituted alkyl.

or a pharmaceutically acceptable salt thereof.

(69)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (67), wherein

R 2d is a hydrogen atom,

or a pharmaceutically acceptable salt thereof.

(70)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (69), wherein

Y 1 is O,

or a pharmaceutically acceptable salt thereof.

(71)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (70), wherein

Y 2 is O,

or a pharmaceutically acceptable salt thereof.

(72)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (71), wherein

R 4 is a hydrogen atom, halogen, or substituted or unsubstituted alkyl,

or a pharmaceutically acceptable salt, thereof.

(73)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (71), wherein

R 4 is a hydrogen atom.

or a pharmaceutically acceptable salt thereof.

(71)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (73), wherein

R 6 is a hydrogen atom, halogen, or substituted or unsubstituted alkyl,

or a pharmaceutically acceptable salt thereof.

(75)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (73), wherein

R 6 is a hydrogen atom,

or a pharmaceutically acceptable salt thereof.

(76)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (75), wherein

R 3a′ is a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted alkenyloxycarbonyl amino, substituted or unsubstituted alkynyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl,

or a pharmaceutically acceptable salt thereof.

(77)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (75), wherein

R 5a′ is a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl,

or a pharmaceutically acceptable salt, thereof.

(78)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (75), wherein

R 5a′ is a hydrogen atom, halogen, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl,

or a pharmaceutically acceptable salt thereof.

(79)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (75), wherein

R 5a′ is a hydrogen atom, halogen, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy,

or a pharmaceutically acceptable salt thereof.

(80)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (75), wherein

R 5a′ is a hydrogen atom,

or a pharmaceutically acceptable salt, thereof.

(81)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (80), wherein

R Y is each independently a hydrogen atom, hydroxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl,

or a pharmaceutically acceptable salt thereof.

(82)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (80), wherein

R Y is each independently a hydrogen atom, hydroxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, or substituted or unsubstituted alkynyloxy,

or a pharmaceutically acceptable salt thereof.

(83)

The compound according to any one of the above (1), (1α), (1α′) and (2) to (80), wherein

R Y is each independently a hydrogen atom, hydroxy, cyano, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy,

or a pharmaceutically acceptable salt thereof.

(84)

The compound according to the above (1), (1α) or (1α′), wherein

or a pharmaceutically acceptable salt thereof.

(85)

The compound according to the above (84), wherein

or a pharmaceutically acceptable salt thereof.

(86)

The compound according to the above (84), wherein

or a pharmaceutically acceptable salt thereof.

(87)

The compound according to the above (84), wherein

or a pharmaceutically acceptable salt thereof.

(88)

The compound according to the above (1), (1α) or (1α′), wherein

the compound is Compound I-0005, Compound I-0006, Compound I-0354, Compound I-0365, Compound I-0372. Compound I-0702, Compound I-0707, Compound I-0842, Compound I-0910, or Compound I-1040,

or a pharmaceutically acceptable salt thereof.

(89)

The compound according to the above (1), (1α) or (1α′), wherein

the compound is Compound I-1041. Compound I-1050, Compound I-1066, Compound I-1108, Compound I-1232, Compound I-1261, Compound I-1281, Compound I-1295, Compound I-1296, or Compound I-1297,

or a pharmaceutically acceptable salt thereof.

(90)

The compound according to the above (1), (1α) or (1α′), wherein

the compound is

or a pharmaceutically acceptable salt thereof.

(91)

The compound according to the above (1). (1α) or (1α′), wherein

the compound is

or a pharmaceutically acceptable salt thereof.

(92)

A pharmaceutical composition comprising the compound according to any one of the above (1) to (91), or a pharmaceutically acceptable salt thereof.

(93)

The pharmaceutical composition according to the above (92) having an antagonistic activity for the P2X7 receptor.

(94)

The compound according to any one of the above (1) to (91), or a pharmaceutically acceptable salt thereof for use in treating and/or preventing a disease associated with the P2X7 receptor.

(95)

A method for treating and/or preventing a disease associated with the P2X7 receptor characterized by administering the compound according to any one of the above (1) to (91), or a pharmaceutically acceptable salt thereof.

(96)

Use of the compound according to any one of the above (1) to (91), or a pharmaceutically acceptable salt thereof for manufacture of a medicament for treating and/or preventing a disease associated with the P2X7 receptor.

(1001) A pharmaceutical composition comprising the compound according to any one of the above (1) to (91), or a pharmaceutically acceptable salt thereof, for oral administration. (1002) The pharmaceutical composition according to (1001), which is a tablet, powder, granule, capsule, pill, film, suspension, emulsion, elixir, syrup, lemonade, spirit, aromatic water, extract, decoction or tincture. (1003) The pharmaceutical composition according to (1002), which is a sugar-coated tablet, film-coated tablet, enteric-coated tablet, sustained-release tablet, troche tablet, sublingual tablet, buccal tablet, chewable tablet, orally dispersing tablet, dry syrup, soft capsule, micro capsule or sustained-release capsule. (1004) A pharmaceutical composition comprising the compound according to any one of the above (1) to (91), or a pharmaceutically acceptable salt thereof, for parenteral administration. (1005) The pharmaceutical composition according to (1004), for dermal, subcutaneous, intravenous, intraarterial, intramuscular, intraperitoneal, transmucosal, inhalation, transnasal, ophthalmic, inner ear or vaginal administration. (1006) The pharmaceutical composition according to (1004) or (1.005), which is injection, infusion, eye drop, nose drop, ear drop, aerosol, inhalation, lotion, impregnation, liniment, mouthwash, enema, ointment, plaster, jelly, cream, patch, cataplasm, external powder or suppository. (1007) A pharmaceutical composition comprising the compound according to any one of the above (1) to (91), or a pharmaceutically acceptable salt thereof, for a pediatric or geriatric patient.

Effect of the Invention

The compounds of the present invention have an antagonistic activity for the P2X7 receptor, and are useful as a therapeutic and/or preventive agent for diseases or conditions associated with the P2X7 receptor.

Terms used in this description are explained below. Each term, unless otherwise indicated, has the same meaning when it is used alone or together with other terms.

The term “consist of” means having only a component.

The term “comprise” means that an element that is not described is not excluded without limitations to a component.

“Halogen” includes a fluorine atom, a chlorine atom, a bromine atom and an iodine atom. A fluorine atom and a chlorine atom are preferable.

“Alkyl” includes a C1 to C15, preferably C1 to C10, more preferably C1 to C6 and further preferably C1 to C4 linear or branched hydrocarbon group. For example, it includes methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, isohexyl, n-heptyl, isoheptyl, n-octyl, isooctyl, n-nonyl, n-decyl and the like.

A preferred embodiment of “alkyl” is methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl or n-pentyl. A more preferred embodiment is methyl, ethyl, n-propyl, isopropyl or tert-butyl.

“Alkenyl” includes a C2 to C15, preferably C2 to C10, more preferably C2 to C6 and further preferably C2 to C4 linear or branched hydrocarbon group having one or more double bond(s) at any position(s). For example, it includes vinyl, allyl, propenyl, isopropenyl, butenyl, isobutenyl, prenyl, butadienyl, pentenyl, isopentenyl, pentadienyl, hexenyl, isohexenyl, hexadienyl, heptenyl, octenyl, nonenyl, decenyl, undecenyl, dodecenyl, tridecenyl, tetradecenyl, pentadecenyl and the like.

A preferred embodiment of “alkenyl” is vinyl, allyl, propenyl, isopropenyl or butenyl.

“Alkynyl” includes a C2 to C10, preferably C2 to C8, more preferably C2 to <16 and further preferably C2 to C4 linear or branched hydrocarbon group having one or more triple bond(s) at any position(s). For example, it includes ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl, octynyl, nonynyl, decynyl and the like. Furthermore, it may have double bond(s) at any position(s).

A preferred embodiment of “alkynyl” is ethynyl, propynyl, butynyl or pentynyl.

“Aromatic carbocycle” means a cyclic aromatic hydrocarbon ring which is monocyclic or polycyclic having two or more rings. For example, it includes benzene, naphthalene, anthracene, phenanthrene and the like.

A preferred embodiment, of “aromatic carbocycle” is benzene.

“Aromatic carbocyclyl” means a cyclic aromatic hydrocarbon group which is monocyclic or polycyclic having two or more rings. For example, it includes phenyl, naphthyl, anthryl, phenanthryl and the like.

A preferred embodiment of “aromatic carbocyclyl” is phenyl.

“Non-aromatic carbocycle” means a cyclic saturated hydrocarbon ring or a cyclic unsaturated non-aromatic hydrocarbon ring, which is monocyclic or polycyclic having two or more rings. “Non-aromatic carbocycle”, which is polycyclic having two or more rings, includes a fused ring wherein a non-aromatic carbocycle, which is monocyclic or polycyclic having two or more rings, is fused with a ring of the above “aromatic carbocycle”.

In addition, the “non-aromatic carbocycle” also includes a ring having a bridge or a ring to form a spiro ring as follows.

A non-aromatic carbocycle which is monocyclic is preferably C3 to C16, more preferably C3 to C12 and further preferably C4 to C8 carbocycle. For example, it includes cyclopropane, cyclobutane, cyclopentane, cyclohexane, cycloheptane, cyclooctane, cyclononane, cyclodecane, cyclopropane, cyclobutene, cyclopentene, cyclohexene, cycloheptene, cyclohexadiene and the like.

A non-aromatic carbocycle which is polycyclic having two or more rings includes, for example, indane, indene, acenaphthalene, tetrahydronaphthalene, fluorene and the like.

“Non-aromatic carbocyclyl” means a cyclic saturated hydrocarbon group or a cyclic unsaturated non-aromatic hydrocarbon group, which is monocyclic or polycyclic having two or more rings. “Non-aromatic carbocyclyl”, which is polycyclic having two or more rings, includes a fused ring group wherein a non-aromatic carbocyclyl, which is monocyclic or polycyclic having two or more rings, is fused with a ring of the above “aromatic carbocyclyl”.

In addition, the “non-aromatic carbocyclyl” also includes a group having a bridge or a group to form a spiro ring as follows:

A non-aromatic carbocyclyl which is monocyclic is preferably C3 to C10, more preferably C3 to C12 and further preferably C4 to C8 carbocyclyl. For example, it includes cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, eyclononyl, cyclodecyl, cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclohexadienyl and the like.

A non-aromatic carbocyclyl which is polycyclic having two or more rings includes, for example, indanyl, indenyl, acenaphthyl, tetrahydronaphthyl, fluorenyl and the like.

“Aromatic heterocyclo” means an aromatic ring, which is monocyclic or polycyclic having two or more rings, containing one or more and same or different of heteroatom(s) selected independently from O, S and N.

“Aromatic heterocyclo”, which is polycyclic having two or more rings, includes a fused ring wherein an aromatic heterocycle, which is monocyclic or polycyclic having two or more rings, is fused with a ring of the above “aromatic carbocycle”.

An aromatic heterocycle which is monocyclic is preferably a 5- to 8-membered and more preferably 5- to 6-membered ring. For example, it includes pyrrole, imidazole, pyrazole, pyridine, pyridazine, pyrimidine, pyrazine, triazole, triazine, tetrazole, furan, thiophene, isoxazole, oxazole, oxadiazole, isothiazole, thiazole, thiadiazole and the like.

An aromatic heterocycle which is bicyclic includes, for example, indole, isoindole, indazole, indolizine, quinoline, isoquinoline, cinnoline, phthalazine, quinazoline, naphthyridine, quinoxaline, purine, pteridine, benzimidazole, benzisoxazole, benzoxazole, benzoxadiazole, benzisothiazole, benzothiazole, benzothiadiazole, benzofuran, isobenzofuran, benzothiophene, benzotriazole, imidazopyridine, triazolopyridine, imidazothiazole, pyrazinopyridazine, oxazolopyridine, thiazolopyridine and the like.

An aromatic heterocycle which is polycyclic having three or more rings includes, for example, carbazole, acridine, xanthene, phenothiazine, phenoxathiine, phenoxazine, dibenzofuran and the like.

“Aromatic heterocyclyl” means an aromatic cyclyl, which is monocyclic or polycyclic having two or more rings, containing one or more and same or different of heteroatom(s) selected independently from O, S and N.

“Aromatic heterocyclyl”, which is polycyclic having two or more rings, includes a fused ring group wherein an aromatic heterocyclyl, which is monocyclic or polycyclic having two or more rings, is fused with a ring of the above “aromatic carbocyclyl”.

An aromatic heterocyclyl which is monocyclic is preferably a 5- to 8-membered and more preferably 5- to 6-membered ring. For example, it includes pyrrolyl, imidazolyl, pyrazolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, triazolyl, triazinyl, tetrazolyl, furyl, thienyl, isoxazolyl, oxazolyl, oxadiazolyl, isothiazolyl, thiazolyl, thiadiazolyl and the like.

An aromatic heterocyclyl which is bicyclic includes, for example, indolyl, isoindolyl, indazolyl, indolizinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, naphthyridinyl, quinoxalinyl, purinyl, pteridinyl, benzimidazolyl, benzisoxazolyl, benzoxazolyl, benzoxadiazolyl, benzisothiazolyl, benzothiazolyl, benzothiadiazolyl, benzofuryl, isobenzofuryl, benzothienyl, benzotriazolyl, imidazopyridyl, triazolopyridyl, imidazothiazolyl, pyrazinopyridazinyl, oxazolopyridyl, thiazolopyridyl and the like.

An aromatic heterocyclyl which is polycyclic having three or more rings includes, for example, carbazolyl, acridinyl, xanthenyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, dibenzofuryl and the like.

“Non-aromatic heterocycle” means a non-aromatic ring, which is monocyclic or polycyclic having two or more rings, containing one or more and same or different of heteroatom(s) selected independently from O, S and N.

“Non-aromatic heterocycle”, which is polycyclic having two or more rings, includes a fused ring wherein a non-aromatic heterocycle, which is monocyclic or polycyclic having two or more ring(s), is fused with a ring of the above “aromatic carbocycle”, “non-aromatic carbocycle” and/or “aromatic heterocycle”. The non-aromatic heterocycle, which is polycyclic having two or more rings, further includes a fused ring wherein an aromatic heterocycle, which is monocyclic or polycyclic having two or more rings, is fused with a ring of the above “non-aromatic carbocycle”.

In addition, the “non-aromatic heterocycle” also includes a ring having a bridge or a ring to form a spiro ring as follows.

A non-aromatic heterocycle which is monocyclic is preferably a 3- to 8-membered and more preferably 5- to 6-membered ring. For example, it includes dioxane, thiirane, oxirane, oxetane, oxathiolane, azetidine, thiane, thiazolidine, pyrrolidine, pyrroline, imidazolidine, imidazoline, pyrazolidine, pyrazoline, piperidine, piperazine, morpholine, thiomorpholine, dihydropyridine, tetrahydropyridino, tetrahydrofuran, tetrahydropyrane, dihydrothiazole, tetrahydrothiazole, tetrahydroisothiazole, dihydrooxazine, hexahydroazepine, tetrahydrodiazepine, tetrahydropyridazine, hexahydropyrimidine, dioxolane, dioxazine, aziridine, dioxoline, oxepane, thiolane, thiine, thiazine and the like.

A non-aromatic heterocycle which is polycyclic having two or more rings includes, for example, indoline, isoindolinel, chromane, isochromane and the like.

“Non-aromatic heterocyclyl” means a non-aromatic cyclyl, which is monocyclic or polycyclic having two or more rings, containing one or more and same or different of heteroatom(s) selected independently from O, S and N.

“Non-aromatic heterocyclyl”, which is polycyclic having two or more rings, includes a fused ring group wherein a non-aromatic heterocycle, which is monocyclic or polycyclic having two or more ring(s), is fused with a ring of the above “aromatic carbocyclyl”, “non-aromatic carbocyclyl” and/or “aromatic heterocyclyl”. The non-aromatic heterocyclyl, which is polycyclic having two or more rings, further includes a fused ring wherein an aromatic heterocyclyl, which is monocyclic or polycyclic having two or more rings, is fused with a ring of the above “non-aromatic carbocyclyl”.

In addition, the “non-aromatic heterocyclyl” also includes a group having a bridge or a group to form a spiro ring as follows:

A non-aromatic heterocyclyl which is monocyclic is preferably a 3- to 8-membered and more preferably 5- to 6-membered ring. For example, it includes dioxanyl, thiiranyl, oxiranyl, oxetanyl, oxathiolanyl, azetidinyl, thienyl, thiazolidinyl, pyrrolidinyl, pyrrolinyl, imidazolidinyl, imidazolinyl, pyrazolidinyl, pyrazolinyl, piperidinyl, piperazinyl, morpholinyl, morpholino, thiomorpholinyl, thiomorpholino, dihydropyridinyl, tetrahydropyridinyl, tetrahydrofuryl, tetrahydropyranyl, dihydrothiazolinyl, totrahydrothiazolinyl, tetrahydroisothiazolinyl, dihydrooxazinyl, hexahydroazepinyl, tetrahydrodiazepinyl, tetrahydropyridazinyl, hexahydropyrimidinyl, dioxolanyl, dioxazinyl, aziridinyl, dioxolinyl, oxepanyl, thiolanyl, thiinyl, thiazinyl and the like.

A non-aromatic heterocyclyl which is polycyclic having two or more rings includes, for example, indolinyl, isoindolinyl, chromanyl, isochromanyl and the like.

“Alkyloxy” means a group wherein the above “alkyl” is bonded to an oxygen atom. For example, it includes methyloxy, ethyloxy, n-propyloxy, isopropyloxy, n-butyloxy, tert-butyloxy, isobutyloxy, sec-butyloxy, pentyloxy, isopentyloxy, hexyloxy and the like.

A preferred embodiment of “alkyloxy” is methyloxy, ethyloxy, n-propyloxy, isopropyloxy or tert-butyloxy.

“Alkenyloxy” means a group wherein the above “alkenyl” is bonded to an oxygen atom. For example, it includes vinyloxy, allyloxy, 1-propenyloxy, 2-butenyloxy, 2-pentenyloxy, 2-hexenyloxy, 2-heptenyloxy, 2-octenyloxy and the like.

“Alkynyloxy” means a group wherein the above “alkynyl” is bonded to an oxygen atom. For example, it includes ethynyloxy, 1-propynyloxy, 2-propynyloxy, 2-butynyloxy, 2-pentynyloxy. 2-hexynyloxy, 2-heptynyloxy, 2-octynyloxy and the like.

“Alkylsulfanyl” means a group wherein a hydrogen atom bonded to a sulfur atom of a sulfanyl group is replaced with the above “alkyl”. For example, it includes methylsulfanyl, ethylsulfanyl, n-propylsulfanyl, isopropylsulfanyl and the like.

“Alkenylsulfonyl” means a group wherein a hydrogen atom bonded to a sulfur atom of a sulfanyl group is replaced with the above “alkenyl”. For example, it includes ethylenylsulfanyl, propenylsulfanyl and the like.

“Alkynylsulfanyl” means a group wherein a hydrogen atom bonded to a sulfur atom of a sulfanyl group is replaced with the above “alkynyl”. For example, it includes ethynylsulfanyl, propynylsulfanyl and the like.

“Alkylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the above “alkyl”. For example, it includes methylamino, ethylamino, isopropylamino and the like. Another hydrogen atom attached to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

A preferred embodiment of “alkylamino” is methylamino or ethylamino.

“Alkenylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the above “alkenyl”. For example, it includes ethylenylamino, propenylamino and the like. Another hydrogen atom attached to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Alkynylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the above “alkynyl”. For example, it includes ethynylamino, propynylamino and the like. Another hydrogen atom attached to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Alkylcarbonyl” means a group wherein the above “alkyl” is bonded to a carbonyl group. For example, it includes methylcarbonyl, ethylcarbonyl, propylcarbonyl, isopropylcarbonyl, tert-butylcarbonyl, isobutylcarbonyl, sec-butylcarbonyl, pentylcarbonyl, isopenthylcarbonyl, hexylcarbonyl and the like.

A preferred embodiment of “alkylcarbonyl” is methylcarbonyl, ethylcarbonyl or n-propylcarbonyl.

“Alkenylcarbonyl” means a group wherein the above “alkenyl” is bonded to a carbonyl group. For example, it includes ethylenylcarbonyl, propenylcarbonyl and the like.

“Alkynylcarbonyl” means a group wherein the above “alkynyl” is bonded to a carbonyl group. For example, it includes ethynylcarbonyl, propynylcarbonyl and the like.

“Alkylsulfonyl” means a group wherein the above “alkyl” is bonded to a sulfonyl group. For example, it includes methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, tert-butylsulfonyl, isobutylsulfonyl, see-butylsulfonyl and the like.

A preferred embodiment, of “alkylsulfonyl” is methylsulfonyl or ethylsulfonyl.

“Alkenylsulfonyl” means a group wherein the above “alkenyl” is bonded to a sulfonyl group. For example, it includes ethylenylsulfonyl, propenylsulfonyl and the like.

“Alkynylsulfinyl” means a group wherein the above “alkynyl” is bonded to a sulfonyl group. For example, it includes ethynyl sulfonyl, propynylsulfonyl and the like.

“Alkylcarbonyloxy” means a group wherein the above “alkylcarbonyl” is bonded to an oxygen atom. For example, it includes methylcarbonyloxy, ethylcarbonyloxy, propylcarbonyloxy, isopropylcarbonyloxy, tert-butylcarbonyloxy, isobutylcarbonyloxy, sec-butylcarbonyloxy and the like.

A preferred embodiment of “alkylcarbonyloxy” is methylcarbonyloxy or ethylcarbonyloxy.

“Alkenylcarbonyloxy” means a group wherein the above “alkenylcarbonyl” is bonded to an oxygen atom. For example, it includes ethylenylcarbonyloxy, propenylcarbonyloxy and the like.

“Alkynylcarbonyloxy” means a group wherein the above “alkynylcarbonyl” is bonded to an oxygen atom. For example, it includes ethynylcarbonyloxy, propenylcarbonyloxy and the like.

“Alkyloxycarbonyl” means a group wherein the above “alkyloxy” is bonded to a carbonyl group. For example, it includes methyloxycarbonyl, ethyloxycarbonyl, propyloxycarbonyl, isopropyloxycarbonyl, tert-butyloxycarbonyl, isobutyloxycarbonyl, sec-butyloxycarbonyl, penthyloxycarbonyl, isopenthyloxycarbonyl, hexyloxycarbonyl and the like.

A preferred embodiment of “alkyloxycarbonyl” is methyloxycarbonyl, ethyloxycarbonyl or propyloxycarbonyl.

“Alkenyloxycarbonyl” means a group wherein the above “alkenyloxy” is bonded to a carbonyl group. For example, it includes ethylenyloxycarbonyl, propenyloxycarbonyl and the like.

“Alkynyloxycarbonyl” means a group wherein the above “alkynyloxy” is bonded to a carbonyl group. For example, it includes ethynyloxycarbonyl, propynyloxycarbonyl and the like.

“Alkylsulfonyloxy” means a group wherein the above “alkylsulfonyl” is bonded to an oxygen atom. For example, it includes methylsulfonyloxy, arylsulfonyloxy, propylsulfonyloxy, isopropylsulfonyloxy, tert-butylsulfonyloxy, isobutyl sulfonyloxy, sec-butylsulfonyloxy and the like.

A preferred embodiment of “alkylsulfonyloxy” is methylsulfonyloxy or ethylsulfonyloxy.

“Alkenylsulfonyloxy” means a group wherein the above “alkenylsulfonyl” is bonded to an oxygen atom. For example, it includes ethylenylsulfonyloxy, propenylsulfonyloxy and the like.

“Alkynylsulfonyloxy” means a group wherein the above “alkynylsulfonyl” is bonded to an oxygen atom. For example, it includes ethynylsulfonyloxy, propynylsulfonyloxy and the like.

“Alkyloxysulfonyl” means a group wherein the above “alkyloxy” is bonded to a sulfonyl group. For example, it includes methyloxysulfonyl, ethyloxysulfonyl, propyloxysulfonyl, isopropyloxysulfonyl, tert-butyloxysulfonyl, isobutyloxysulfonyl, sec-butyloxysulfonyl, pentyloxysulfonyl, isopentyloxysulfonyl, hexyloxysulfenyl and the like.

A preferred embodiment of “alkyloxysulfonyl” is methyloxysulfonyl, ethyloxysulfonyl, or propyloxysulfonyl.

“Alkenyloxysulfonyl” means a group wherein the above “alkenyloxy” is bonded to a sulfonyl group. For example, it includes ethylenyloxysulfonyl, propenyloxysulfonyl and the like.

“Alkynyloxysulfonyl” means a group wherein the above “alkynyloxy” is bonded to a sulfonyl group. For example, it includes ethynyloxysulfonyl, propynyloxysulfonyl and the like.

“Alkylcarbamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a carbamoyl group is replaced with the above “alkyl”. For example, it includes methylcarbamoyl, ethylcarbamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the carbamoyl group may be replaced with the above “alkyl”.

“Alkenylcarbamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a carbamoyl group is replaced with the above “alkenyl”. For example, it includes ethylenylcarbamoyl, propenylcarbamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the carbamoyl group may be replaced with the above “alkyl”.

“Alkynylcarbamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a carbamoyl group is replaced with the above “alkynyl”. For example, it includes ethynylcarbamoyl, propynyl carbamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the carbamoyl group may be replaced with the above “alkyl”.

“Alkylsulfamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a sulfamoyl group is replaced with the above “alkyl”. For example, it includes methylsulfamoyl, dimethylsulfamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the sulfamoyl group may be replaced with the above “alkyl”.

“Alkenylsulfamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a sulfamoyl group is replaced with the above “alkenyl”. For example, it includes ethylenylsulfamoyl, propenylsulfamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the carbamoyl group may be replaced with the above “alkyl”.

“Alkynylsulfamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a sulfamoyl group is replaced with the above “alkynyl”. For example, it includes ethynylsulfamoyl, propynylsulfamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the carbamoyl group may be replaced with the above “alkyl”.

“Alkylcarbonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “alkylcarbonyl”. For example, it includes methylcarbonylamino, ethylcarbonylamino, propylcarbonylamino, isopropylcarbonylamino, tert-butylcarbonylamino, isobutylcarbonylamino, sec-butylcarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

A preferred embodiment of “alkylcarbonylamino” is methylcarbonylamino or ethylcarbonylamino.

“Alkenylcarbonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “alkenylcarbonyl”. For example, it includes ethylenylcarbonylamino, propenylcarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Alkynylcarbonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “alkynylcarbonyl”. For example, it includes ethynylcarbonylamino, propynylcarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Alkylsulfonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “alkylsulfonyl”. For example, it includes methylsulfonylamino, ethylsulfonylamino, propylsulfonylamino, isopropylsulfonylamino, tert-butylsulfonylamino, isobutylsulfonylamino, sec-butylsulfonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

A preferred embodiment, of “alkylsulfonylamino” is methylsulfonylamino or ethylsulfonylamino.

“Alkonylsulfonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “alkenylsulfonyl”. For example, it includes ethylenylsulfonylamino, propenylsulfonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Alkynylsulfonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “alkynylsulfonyl”. For example, it includes ethynylsulfonylamino, propynylsulfonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Alkyloxycarbonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “alkyloxycarbonyl”. For example, it includes methyloxycarbonylamino, ethyloxycarbonylamino, propyloxycarbonyl amino, isopropyloxycarbonyl amino, tert-butyloxycarbonylamino, isobutyloxycarbonylamino, sec-butyloxycarbonylamino, pentyloxycarbonylamino, isopentyloxycarbonylamino, hexyloxycarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

A preferred embodiment of “alkyloxycarbonyl” is methyloxycarbonylamino, ethyloxycarbonylamino, propyloxycarbonylamino and the like.

“Alkenyloxycarbonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “alkenyloxycarbonyl”. For example, it includes ethylenyloxycarbonylamino, propenyloxycarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Alkynyloxycarbonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “alkynyloxycarbonyl”. For example, it includes ethynyloxycarbonylamino, propynyloxycarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Haloalkyl” moans a group wherein one or more “halogen” described above is bonded to the above “alkyl”. For example, it includes monofluoromethyl, monofluoroethyl, monofluoropropyl, 2,2,3,3,3-pentafluoropropyl, monochloromethyl, trifluoromethyl, trichloromethyl. 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 1,2-dibromoethyl, 1,1,1-trifluoropropan-2-yl and the like.

A preferred embodiment, of “haloalkyl” is trifluoromethyl or trichloromethyl.

“Haloalkyloxy” means a group wherein the above “haloalkyl” is bonded to an oxygen atom. For example, it includes monofluoromethoxy, monofluoroethoxy, trifluoromethoxy, trichloromethoxy, trifluoroethoxy, trichloroethoxy and the like.

A preferred embodiment of “haloalkyloxy” is trifluoromethoxy or trichloromethoxy.

“Haloalkylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of on amino group is replaced with the above “haloalkyl”. For example, it includes monofluoromethyl amino, monofluoroethylamino, trifluoromethylamine, trichloromethylamino, trifluoroethylamino, trichloroethylamine and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl” or the above “haloalkyl”.

A preferred embodiment of “haloalkylamino” is trifluoromethylamine or trichloromethylamino.

“Haloalkylsulfanyl” means a group wherein the above “haloalkyl” is bonded to a sulfanyl group. For example, it includes monofluoromethylsulfanyl, monofluoroethylsulfanyl, trifluoromethylsulfanyl, trichloromethyl sulfanyl, trifluoroethylsulfonyl, trichloroethylsulfanyl and the like.

A preferred embodiment of “haloalkylsulfanyl” is trifluoromethylsulfanyl or trichloromethylsulfonyl.

“Haloalkylcarbonyl” means a group wherein the above “haloalkyl” is bonded to a carbonyl group. For example, it includes monofluoromothylcarbonyl, monofluoroethylcarbonyl, trifluoromethylcarbonyl, trichloromethylcarbonyl, trifluoroethylcarbonyl, trichloroethylcarbonyl and the like.

A preferred embodiment of “haloalkylcarbonyl” is trifluoromethylcarbonyl or trichloromethylcarbonyl.

“Haloalkylsulfonyl” means a group wherein the above “haloalkyl” is bonded to a sulfonyl group. For example, it includes monofluoromethylsulfonyl, monofluoroethylsulfonyl, trifluoromethylsulfonyl, trichloromethylsulfonyl, trifluoroethylsulfonyl, trichloroethylsulfonyl and the like.

A preferred embodiment of “haloalkylsulfonyl” is trifluoromethylsulfonyl or trichloromethylsulfonyl.

“Haloalkylcarbamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a carbamoyl group is replaced with the above “haloalkyl”. For example, it includes monofluoromethylcarbamoyl, monofluoroethylcarbamoyl, trifluoromethylcarbamoyl, trichloromethylcarbamoyl, trifluoroethylcarbamoyl, trichloroethylcorbamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the carbamoyl group may be replaced with the above “alkyl” or the above “haloalkyl”.

A preferred embodiment, of “haloalkylcarbamoyl” is trifluoromethylcarbamoyl or trichloromethylcarbamoyl.

“Haloalkylsulfamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a sulfamoyl group is replaced with the above “haloalkyl”. For example, it includes monofluoromethylsulfamoyl, monofluoroethylsulfamoyl, trifluoromethylsulfainoyl, trichloromethylsulfamoyl, trifluo methylsulfamoyl, trichloroethylsulfamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the sulfamoyl group may be replaced with the above “alkyl” or the above “haloalkyl”.

A preferred embodiment of “haloalkylsulfamoyl” is trifluoromethylsulfamoyl or trichloromethylsulfamoyl.

“Haloalkylcarbonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “haloalkylcarbonyl”. For example, it includes monofluoromethylcarbonylamino, monofluoroethylcarbonylamino, trifluoromethylcarbonylamino, trichloromethylcarbonylamino, trifluoroethylcarbonylamino, trichloroethylcarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl” or the above “haloalkyl”.

A preferred embodiment of “haloalkylcarbonylamino” is trifluoromethylcarbonylamino or trichloromethylcarbonylamino.

“Haloalkylsulfonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “haloalkylsulfonyl”. For example, it includes monofluoromethylsulfonylamino, monofluoroethyl sulfonyl amino, trifluoromethylsulfonylamino, trichloromethylsulfonylamino, trifluoroethylsulfonylamino, trichloroethylsulfonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl” or the above “haloalkyl”.

A preferred embodiment of “haloalkylsulfonylamino” is trifluoromethylsulfonylamino or trichloromethylsulfonylamino.

The “aromatic carbocycle” part of “aromatic carbocyclyloxy”, “aromatic carbocyclylamino”, “aromatic carbocyclylsulfanyl”, “aromatic carbocyclylcarbonyl”, “aromatic carbocyclylsulfonyl”, “aromatic carbocyclylcarbonyloxy”, “aromatic carbocyclylsulfonyloxy”, “aromatic carbocyclyloxycarbonyl”, “aromatic carbocyclyloxysulfonyl”, “aromatic carbocyclylcarbamoyl”, “aromatic carbocyclylsulfamoyl”, “aromatic carbocyclylcarbonylamino”, “aromatic carbocyclylsulfonylamino”, and “aromatic carbocyclyloxycarbonylamino” is the same as the above “aromatic carbocyclyl”.

“Aromatic carbocyclyloxy” means a group wherein “aromatic carbocycle” is bonded to an oxygen atom. For example, it includes phenyloxy, naphthyloxy and the like.

“Aromatic carbocyclylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the “aromatic carbocycle”. For example, it includes phenylamino, naphthylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Aromatic carbocyclylsulfanyl” means a group wherein a hydrogen atom bonded to a sulfur atom of a sulfanyl group is replaced with “aromatic carbocycle”. For example, it includes phenylsulfanyl, naphthylsulfanyl and the like.

“Aromatic carbocyclylcarbonyl” means a group wherein “aromatic carbocycle” is bonded to a carbonyl group. For example, it includes phenylcarbonyl, naphthylcarbonyl and the like.

“Aromatic carbocyclylsulfonyl” means a group wherein “aromatic carbocycle” is bonded to a sulfonyl group. For example, it, includes phenylsulfonyl, naphthylsulfonyl and the like.

“Aromatic carbocyclylcarbonyloxy” means a group wherein the above “aromatic carbocyclylcarbonyl” is bonded to an oxygen atom. For example, it includes phenylcarbonyloxy, naphthylcarbonyloxy and the like.

“Aromatic carbocyclylsulfonyloxy” means a group wherein the above “aromatic carbocyclylsulfonyl” is bonded to an oxygen atom. For example, it includes phenylsulfonyloxy, naphthylsulfonyloxy and the like.

“Aromatic carbocyclyloxycarbonyl” means a group wherein the above “aromatic carbocyclyloxy” is bonded to a carbonyl group. For example, it includes phenyloxycarbonyl, naphthyloxycarbonyl and the like.

“Aromatic carbocycyloxysulfonyl” means a group wherein the above “aromatic carbocyclyloxy” is bonded to a sulfonyl group. For example, it includes phenyloxysulfonyl, naphthyloxysulfonyl and the like.

“Aromatic carbocyclylcarbamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a carbamoyl group is replaced with the “aromatic carbocycle”. For example, it includes phenylcarbamoyl, naphthylcarbamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the carbamoyl group may be replaced with the above “alkyl”.

“Aromatic carbocyclylsulfamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a sulfamoyl group is replaced with the “aromatic carbocycle”. For example, it includes phenylsulfamoyl, naphthylsulfoniyl and the like. Another hydrogen atom bonded to the nitrogen atom of the sulfamoyl group may be replaced with the above “alkyl”.

“Aromatic carbocyclylcarbonylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the above “aromatic carbocyclylcarbonyl”. For example, it includes phenylcarbonylamino, naphthylcarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Aromatic carbocyclylsulfonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “aromatic carbocyclylsulfonyl”. For example, it includes phenylsulfonylamino, naphthylsulfonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Aromatic carbocyclyloxycarbonylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the above “aromatic carbocyclyloxycarbonyl”. For example, it includes phenyloxycarbonylamino, naphthyloxycarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

The “non-aromatic carbocycle” part of “non-aromatic carbocyclyloxy”, “non-aromatic carbocyclylamino”, “non-aromatic carbocyclylsulfanyl”, “non-aromatic carbocyclylcarbonyl”, “non-aromatic carbocyclylsulfonyl”, “non-aromatic carbocyclylcarbonyloxy”, “non-aromatic carbocyclylsulfonyloxy”, “non-aromatic carbocyclyloxycarbonyl”, “non-aromatic carbocyclyloxysulfonyl”, “non-aromatic carbocyclylcarbamoyl”, “non-aromatic carbocyclylsulfamoyl”, “non-aromatic carbocyclylcarbonylamino”, “non-aromatic carbocyclylsulfonylamino”, and “non-aromatic carbocyclyloxycarbonylamino” is the same as the above “non-aromatic carbocyclyl”.

“Non-aromatic carbocyclyloxy” means a group wherein “non-aromatic carbocycle” is bonded to an oxygen atom. For example, it includes cyclopropyloxy, cyclohexyloxy, cyclohexenyloxy and the like.

“Non-aromatic carbocyclylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the “non-aromatic carbocycle”. For example, it includes cyclopropylamino, cyclohexylamino, cyclohexenylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Non-aromatic carbocyclylsulfanyl” means a group wherein a hydrogen atom bonded to a sulfur atom of a sulfanyl group is replaced with “non-aromatic carbocycle”. For example, it includes cyclopropylsulfanyl, cyclohexylsulfanyl, cyclohexenylsulfanyl and the like.

“Non-aromatic carbocyclylcarbonyl” means a group wherein “non-aromatic carbocycle” is bonded to a carbonyl group. For example, it includes cyclopropylcarbonyl, cyclohexylcarbonyl, cyclohexenylcarbonyl and the like.

“Non-aromatic carbocyclylsulfonyl” means a group wherein “non-aromatic carbocycle” is bonded to a sulfonyl group. For example, it includes cyclopropylsulfonyl, cyclohexylsulfonyl, cyclohexenylsulfonyl and the like.

“Non-aromatic carbocyclylcarbonyloxy” means a group wherein the above “non-aromatic carbocyclylcarbonyl” is bonded to an oxygen atom. For example, it includes cyclopropylcarbonyloxy, cyclohexylcarbonyloxy, cyclohexenylcarbonyloxy and the like.

“Non-aromatic carbocyctylsulfonyloxy” means a group wherein the above “non-aromatic carbocyclylsulfonyl” is bonded to an oxygen atom. For example, it includes cyclopropylsulfonyloxy, cyclohexylsulfonyloxy, cyclohexenylsulfonyloxy and the like.

“Non-aromatic carbocyclyloxycarbonyl” means a group wherein the above “non-aromatic carbocyclyloxy” is bonded to a carbonyl group. For example, it includes cyclopropyloxycarbonyl, cyclohexyloxycarbonyl, cyclohexenyloxycarbonyl and the like.

“Non-aromatic carbocyclyloxyaulfonyl” means a group wherein the above “non-aromatic carbocyclyloxy” is bonded to a sulfonyl group. For example, it includes cyclopropyloxysulfonyl, cyclohexyloxysulfonyl, cyclohexenyloxysulfonyl and the like.

“Non-aromatic carbocyclylcarbamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a carbamoyl group is replaced with the “non-aromatic carbocycle”. For example, it includes cyclopropylcarbamoyl, cyclohexylcarbamoyl, cyclohexenylcarbamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the carbamoyl group may be replaced with the above “alkyl”.

“Non-aromatic carbocyclylsulfamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a sulfamoyl group is replaced with the “non-aromatic carbocycle”. For example, it includes cyclopropylsulfamoyl, cyclohexylsulfamoyl, cyclohexenylsulfamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the sulfamoyl group may be replaced with the above “alkyl”.

“Non-aromatic carbocyclylcarbonylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the above “non-aromatic carbocyclylcarbonyl”. For example, it includes cyclopropylcarbonyl amino, cyclohexylcarbonylamino, cyclohexenylcarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Non-aromatic carbocyclylsulfonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “non-aromatic carbocyclylsulfonyl”. For example, it includes cyclopropylsulfonylamino, cyclo hexylsulfonyl amino, cyclohexenylsulfonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Non-aromatic carbocyclyloxycarbonylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the above “non-aromatic carbocyclyloxycarbonyl”. For example, it includes cyclopropyloxycarbonylamino, cyclohexyloxycarbonylamino, cyclohexanyloxycarbonyl amino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

The “aromatic heterocycle” part of “aromatic heterocyclyloxy”, “aromatic heterocyclylamino”, “aromatic heterocyclylsulfanyl”, “aromatic heterocyclylcarbonyl”, “aromatic heterocyclylsulfonyl”, “aromatic heterocyclylcarbonyloxy”, “aromatic heterocyclylsulfonyloxy”, “aromatic heterocyclyloxycarbonyl”, “aromatic heterocyclyloxysulfonyl”, “aromatic heterocyclylcarbamoyl”, “aromatic heterocyclylsulfamoyl”, “aromatic heterocyclylcarbonylamino”, “aromatic heterocyclylsulfonylamino”, and “aromatic hoterocyclyloxycarbonylamino” is the same as the above “aromatic heterocyclyl”.

“Aromatic heterocyclyloxy” means a group wherein “aromatic heterocycle” is bonded to an oxygen atom. For example, it includes pyridyloxy, oxazolyloxy and the like.

“Aromatic heterocyclylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the “aromatic heterocycle”. For example, it includes pyridylamino, oxazolylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Aromatic heterocyclylsulfanyl” means a group wherein a hydrogen atom bonded to a sulfur atom of a sulfanyl group is replaced with “aromatic heterocycle”. For example, it includes pyridylsulfanyl, oxazol ylsulfanyl and the like.

“Aromatic heterocyclylcarbonyl” means a group wherein “aromatic heterocycle” is bonded to a carbonyl group. For example, it includes pyridylcarbonyl, oxazolylcarbonyl and the like.

“Aromatic heterocyclylsulfonyl” means a group wherein “aromatic heterocycle” is bonded to a sulfonyl group. For example, it includes pyridylsulfonyl, oxazolylsulfonyl and the like.

“Aromatic heterocyclylcarbonyloxy” means a group wherein the above “aromatic heterocyclylcarbonyl” is bonded to an oxygen atom. For example, it includes pyridylcarbonyloxy, oxazolylcarbonyloxy and the like.

“Aromatic hetorocyclylsulfonyloxy” means a group wherein the above “aromatic heterocyclylsulfonyl” is bonded to an oxygen atom. For example, it includes pyridylsulfonyloxy, oxazolylsulfonyloxy and the like.

“Aromatic heterocyclyloxycarbonyl” means a group wherein the above “aromatic heterocyclyloxy” is bonded to a carbonyl group. For example, it includes pyridyloxycarbonyl, oxazolyloxycarbonyl and the like.

“Aromatic heterocyclyloxysulfonyl” means a group wherein the above “aromatic heterocyclyloxy” is bonded to a sulfonyl group. For example, it includes pyridyloxysulfonyl, oxazolyloxysulfonyl and the like.

“Aromatic heterocyclylcarbamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a carbamoyl group is replaced with the “aromatic heterocycle”. For example, it includes pyridylcarbamoyl, oxazol ylcarbamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the carbamoyl group may be replaced with the above “alkyl”.

“Aromatic heterocycylsulfamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a sulfamoyl group is replaced with the “aromatic heterocycle”. For example, it includes pyridylsulfamoyl, oxazolylsulfamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the sulfamoyl group may be replaced with the above “alkyl”.

“Aromatic heterocyclylcarbonyl amino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the above “aromatic heterocyclylcarbonyl”. For example, it includes pyridylcarbonylamino, oxazolylcarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Aromatic heterocyclylsulfonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “aromatic heterocyclylsulfonyl”. For example, it includes pyridylsulfonylamino, oxazolylsulfonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Aromatic heterocyclyloxycarbonylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the above “aromatic heterocyclyloxycarbonyl”. For example, it includes pyridyloxycarbonylamino, oxazolyloxycarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

The “non-aromatic heterocycle” part of “non-aromatic heterocyclyloxy”, “non-aromatic heterocyclylamino”, “non-aromatic heterocyclyl sulfanyl”, “non-aromatic heterocyclylcarbonyl”, “non-aromatic heterocyclylsulfonyl”, “non-aromatic heterocyclylcarbonyloxy”, “non-aromatic heterocyclylsulfonyloxy”, “non-aromatic heterocyclyloxycarbonyl”, “non-aromatic heterocyclyloxysulfonyl”, “non-aromatic heterocyclylcarbamoyl”, “non-aromatic heterocyclylsulfamoyl”, “non-aromatic heterocyclylcarbonylamino”, “non-aromatic heterocyclylsulfonylamino”, and “non-aromatic heterocyclyloxycarbonylamino” is the same as the above “non-aromatic heterocyclyl”.

“Non-aromatic heterocyclyloxy” means a group wherein “non-aromatic heterocycle” is bonded to an oxygen atom. For example, it includes piperidinyloxy, tetrahydrofuryloxy and the like.

“Non-aromatic heterocyclylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the “non-aromatic heterocycle”. For example, it includes piperidinylamino, tetrahydrofurylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Non-aromatic heterocyclylsulfanyl” means a group wherein a hydrogen atom bonded to a sulfur atom of a sulfanyl group is replaced with “non-aromatic heterocycle”. For example, it includes piperidinylsulfonyl, tetrahydrofurylsulfanyl and the like.

“Non-aromatic heterocyclylcarbonyl” means a group wherein “non-aromatic heterocycle” is bonded to a carbonyl group. For example, it includes piperidinylcarbonyl, tetrahydrofurylcarbonyl and the like.

“Non-aromatic heterocyclylsulfonyl” means a group wherein “non-aromatic heterocycle” is bonded to a sulfonyl group. For example, it includes piperidinylsulfonyl, tetrahydrofurylsulfonyl and the like.

“Non-aromatic hoterocyclylcarbonyloxy” moans a group wherein the above “non-aromatic heterocyclylcarbonyl” is bonded to an oxygen atom. For example, it includes piperidinylcarbonyloxy, tetrahydrofurylcarbonyloxy and the like.

“Non-aromatic heterocyclylsulfonyloxy” moans a group wherein the above “non-aromatic heterocyclylsulfonyl” is bonded to an oxygen atom. For example, it includes piperidinylsulfonyloxy, tetrahydrofuryl sulfonyloxy and the like.

“Non-aromatic heterocyclyloxycarbonyl” means a group wherein the above “non-aromatic heterocyclyloxy” is bonded to a carbonyl group. For example, it includes piperidinyloxycarbonyl, tetrahydrofuryloxycarbonyl and the like.

“Non-aromatic heterocyclyloxysulfonyl” means a group wherein the above “non-aromatic heterocyclyloxy” is bonded to a sulfonyl group. For example, it includes piperidinyloxysulfonyl, tetrahydrofuryloxysulfonyl and the like.

“Non-aromatic heterocyclylcarbamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a carbamoyl group is replaced with the “non-aromatic heterocycle”. For example, it includes piperidinylcarbamoyl, tetrahydrofurylcarbamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the carbamoyl group may be replaced with the above “alkyl”.

“Non-aromatic heterocyclylsulfamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a sulfamoyl group is replaced with the “non-aromatic heterocycle”. For example, it includes piperidinylsulfamoyl, tetrahydrofurylsulfamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the sulfamoyl group may be replaced with the above “alkyl”.

“Non-aromatic heterocyclylcarbonylamino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the above “non-aromatic heterocyclylcarbonyl”. For example, it includes piperidinylcarbonylamino, tetrahydrofurylcarbonylamiuo and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Non-aromatic heterocyclylsulfonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “non-aromatic heterocyclylsulfonyl”. For example, it includes piperidinylsulfonylamino, tetrahydrofurylsulfonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Non-aromatic heterocyclyloxycarbonyl amino” means a group wherein a hydrogen atom attached to a nitrogen atom of an amino group is replaced with the above “non-aromatic heterocyclyloxycarbonyl”. For example, it includes piperidinyloxycarbonylamino, tetrahydrofuryloxycarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl”.

“Haloalkyl” means a group wherein one or more “halogen” described above is bonded to the above “alkyl”. For example, it includes monofluoromethyl, monofluoroethyl, monofluoropropyl, 2,2,3,3,3-pentafluoropropyl, monochloromethyl, trifluoromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 1,2-dibromoethyl, 1,1,1-trifluoropropan-2-yl and the like.

A preferred embodiment of “haloalkyl” is trifluoromethyl or trichloromethyl.

“Haloalkyloxy” means a group wherein the above “haloalkyl” is bonded to an oxygen atom. For example, it includes monofluoromethoxy, Monofluoroethoxy, trifluoromethoxy, trichloromethoxy, trifluoroethoxy, trichloroethoxy and the like.

A preferred embodiment of “halonlkyloxy” is trifluoromethoxy or trichloromethoxy.

“Haloalkylamino” moans a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “haloalkyl”, For example, it includes monofluoromethylamino, monofluoroethylamino, trifluoromethylamine, trichloromethylamino, trifluoroethylamino, trichloroethylamine and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl” or the above “haloalkyl”.

A preferred embodiment of “haloalkylamino” is trifluoromethyl amino or trichloromethylamino.

“Haloalkylsulfonyl” means a group wherein the above “haloalkyl” is bonded to a sulfanyl group. For example, it includes monofluoromethyl sulfanyl, monofluoroethylsulfanyl, trifluoromethylsulfanyl, trichloromethylsulfonyl, trifluoroethylsulfonyl, trichloroethylsulfanyl and the like.

A preferred embodiment of “haloalkylsulfanyl” is trifluoromethylsulfanyl or trichloromethylsulfanyl.

“Haloalkylcarbonyl” means a group wherein the above “haloalkyl” is bonded to a carbonyl group. For example, it includes monofluoromethylcarbonyl, monofluoroethylcarbonyl, trifluoromethylcarbonyl, trichloromethylcarbonyl, trifluoroethylcarbonyl, trichloroethylcarbonyl and the like.

A preferred embodiment of “haloalkylcarbonyl” is trifluoromethylcarbonyl or trichloromethylcarbonyl.

“Haloalkylsulfonyl” means a group wherein the above “haloalkyl” is bonded to a sulfonyl group. For example, it includes monofluoromethylsulfonyl, monofluoroethylsulfonyl, trifluoromethylsulfonyl, trichloromethylsulfonyl, trifluoroethylsulfonyl, trichloroethyl sulfonyl and the like.

A preferred embodiment of “haloalkylsulfonyl” is trifluoromethylsulfonyl or trichloromethylsulfonyl.

“Haloalkylcorbamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a carbamoyl group is replaced with the above “haloalkyl”. For example, it includes monofluoromethylcarbamoyl, monofluoroethylcarbamoyl, trifluoromethylcarbamoyl, trichloromethylcarbamoyl, trifluoroethylcarbamoyl, trichloroethylcarbamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the carbamoyl group may be replaced with the above “alkyl” or the above “haloalkyl”.

A preferred embodiment of “haloalkylcarbamoyl” is trifluoromethylcarbamoyl or trichloromethylcarbamoyl.

“Haloalkylsulfamoyl” means a group wherein a hydrogen atom bonded to a nitrogen atom of a sulfamoyl group is replaced with the above “haloalkyl”. For example, it includes monofluoromethylsulfamoyl, monofluoroethylsulfamoyl, trifluoromethylsulfamoyl, trichloromethylsulfamoyl, trifluoroethylsulfamoyl, trichloroethylsulfamoyl and the like. Another hydrogen atom bonded to the nitrogen atom of the sulfamoyl group may be replaced with the above “alkyl” or the above “haloalkyl”.

A preferred embodiment of “haloalkylsulfamoyl” is trifluoromethylsulfamoyl or trichloromethylsulfamoyl.

“Haloalkylcarbonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “haloalkylcarbonyl”. For example, it includes monofluoromethylcarbonylamino, monofluoroethylcarbonylamino, trifluoromethylcarbonylamino, trichloromethylcarbonylamino, trifluoroethylcarbonylamino, trichloroethylcarbonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl” or the above “haloalkyl”.

A preferred embodiment of “haloalkylcarbonylamino” is trifluoromethylcarbonylamino or trichloromethylcarbonylamino.

“Haloalkylsulfonylamino” means a group wherein a hydrogen atom bonded to a nitrogen atom of an amino group is replaced with the above “haloalkylsulfonyl”. For example, it includes monofluoromethylsulfonylamino, monofluoroethylsulfonylamino, trifluoromethylsulfonylamino, trichloromethylsulfonylamino, trifluoroethylsulfonylamino, trichloroethylsulfonylamino and the like. Another hydrogen atom bonded to the nitrogen atom of the amino group may be replaced with the above “alkyl” or the above “haloalkyl”.

A preferred embodiment of “haloalkylsulfonylamino” is trifluoromethylsulfonylamino or trichloromethylsulfonylamino.

“Haloalkylcarbonyloxy” means a group wherein the above “haloalkylcarbonyl” is bonded to an oxygen atom. For example, it includes monofluoromethylcarbonyloxy, monofluoroethylcarbonyloxy, trifluoromethylcarbonyloxy, (trichloromethylcarbonyloxy, trifluoroethylcarbonyloxy, trichloroethylcarbonyloxy and the like.

A preferred embodiment of “haloalkylcarbonyloxy” is trifluoromethylcarbonyloxy or trichloromethylcarbonyloxy.

“Haloalkylsulfonyloxy” means a group wherein the above “haloalkylsulfonyl” is bonded to an oxygen atom. For example, it includes monofluoromethylsulfonyloxy, monofluoroetliylsulfonyloxy, trifluoromethylsulfonyloxy, trichloromethyl sulfonyloxy, trifluoroethylsulfonyloxy, trichloroethylsulfonyloxy and the like.

A preferred embodiment of “haloalkylsulfonyloxy” is trifluoromethylsulfonyloxy or trichloromethylsulfonyloxy.

“Haloalkyloxycarbonyl” means a group wherein the above “haloaryloxy” is bonded to a carbonyl group. For example, it includes monofluoromethyl oxycarbonyl, monofluoroethyloxycarbonyl, trifluoromethyloxycarbonyl, trichloromethyloxycarbonyl, trifluoroethyloxycarbonyl, trichloroethyloxycarbonyl and the like.

A preferred embodiment of “haloalkyloxycarbonyl” is trifluoromethyloxycarbonyl or trichloromethyloxycarbonyl.

“Haloalkyloxysulfonyl” means a group wherein the above “haloaryloxy” is bonded to a sulfonyl group. For example, it includes monofluoromethyloxysulfonyl, monofluoroethyloxysulfonyl, trifluoromethyl oxysulfonyl, trichloromethyloxy sulfonyl, trifluoroethyloxysulfonyl, trichloroethyloxysulfonyl and the like.

A preferred embodiment of “haloalkyloxysulfonyl” is trifluoromethyl oxysulfonyl or trichloromethyloxysulfonyl.

The substituents of “substituted or unsubstituted alkyl” include the substituent group A. A carbon atom at any position(s) may be bonded to one or more group(s) selected from the substituent group A.

The substituent group A: halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group C, alkylamino optionally substituted with one or more group(s) selected from the substituent group C, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group C, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent, group C, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group C, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent, group C, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group C, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group C, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group C, alkylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group C, alkyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group C, alkylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group C, aryloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group C, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent, group E, non-aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfonylamino optionally substituted with one or more groups) selected from the substituent group E, aromatic heterocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocycyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent, group E, aromatic heterocyclyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclyloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclyloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent, group E, and non-aromatic heterocyclylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group E.

The substituents of “substituted or unsubstituted alkenyl”, “substituted or unsubstituted alkynyl”, “substituted or unsubstituted alkyloxy”, “substituted or unsubstituted alkenyloxy”, “substituted or unsubstituted alkynyloxy”, “substituted or unsubstituted alkylsulfanyl”, “substituted or unsubstituted alkenylsulfonyl”, “substituted or unsubstituted alkynylsulfanyl”, “substituted or unsubstituted alkylamino”, “substituted or unsubstituted alkenylamino”, “substituted or unsubstituted alkynylamino”, “substituted or unsubstituted alkylcarbonyl”, “substituted or unsubstituted alkenylcarbonyl”, “substituted or unsubstituted alkynylcarbonyl”, “substituted or unsubstituted alkylsulfonyl”, “substituted or unsubstituted alkenylsulfonyl”, “substituted or unsubstituted alkynylsulfonyl”, “substituted or unsubstituted alkylcarbonyloxy”, “substituted or unsubstituted alkenylcarbonyloxy”, “substituted or unsubstituted alkynylcarbonyloxy”, “substituted or unsubstituted alkyloxycarbonyl”, “substituted or unsubstituted alkenyloxycarbonyl”, “substituted or unsubstituted alkynyloxycarbonyl”, “substituted or unsubstituted alkylsulfonyloxy”, “substituted or unsubstituted alkenylsulfonyloxy”, “substituted or unsubstituted alkynylsulfonyloxy”, “substituted or unsubstituted aryloxysulfonyl”, “substituted or unsubstituted alkenyloxysulfonyl”, “substituted or unsubstituted alkynyloxysulfonyl”, “substituted or unsubstituted alkylcarbamoyl”, “substituted or unsubstituted nonylcarbamoyl”, “substituted or unsubstituted alkynylcarbamoyl”, “substituted or unsubstituted alkylsulfamoyl”, “substituted or unsubstituted alkenylsulfamoyl”, “substituted or unsubstituted alkynylsulfamoyl”, “substituted or unsubstituted alkylcarbonylamino”, “substituted or unsubstituted alkenylcarbonylamino”, “substituted or unsubstituted alkynylcarbonylamino”, “substituted or unsubstituted alkylsulfonylamino”, “substituted or unsubstituted alkenylsulfonylamino”, “substituted or unsubstituted alkyloxycarbonylamino”, “substituted or unsubstituted alkenyloxycarbonylamino”, and “substituted or unsubstituted alkynyloxycarbonylamino” include the substituent group B. A carbon atom at arty position(s) may be bonded to one or more group(s) selected from the substituent group B.

The substituent group B: halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group B, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group (a) selected from the substituent group D, alkylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group D, aryloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent, group E, aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent, group E, aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbonyl optionally substituted with one or more group (a) selected from the substituent group E, non-aromatic carbocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclyl sulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent, group E, non-aromatic carbocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent, group E, non-aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclyloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclyloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyl carbonyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclyl sulfonyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group E, and non-aromatic heterocyclylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group E.

The substituents on the rings of “aromatic carbocycle”, “non-aromatic carbocycle”, “aromatic heterocycle”, and “non-aromatic heterocycle” of

“substituted or unsubstituted aromatic carbocycle”, “substituted or unsubstituted non-aromatic carbocycle”, “substituted or unsubstituted aromatic heterocycle”, and “substituted or unsubstituted non-aromatic heterocycle”,

“substituted or unsubstituted 6-membered aromatic carbocycle”, “substituted or unsubstituted 5- to 6-membered non-aromatic carbocycle”, “substituted or unsubstituted 5- to 6-membered aromatic heterocycle”, and “substituted or unsubstituted 5- to 6-membered non-aromatic heterocycle”.

“substituted or unsubstituted aromatic carbocyclyl”, “substituted or unsubstituted non-aromatic carbocyclyl”, “substituted or unsubstituted aromatic heterocyclyl”, and “substituted or unsubstituted non-aromatic heterocyclyl”,

“substituted or unsubstituted 6- to 10-membered aromatic carbocyclyl”, “substituted or unsubstituted 3- to 10-membered non-aromatic carbocyclyl”, “substituted or unsubstituted 5- to 10-membered aromatic heterocyclyl”, and “substituted or unsubstituted 3- to 10-membered non-aromatic heterocyclyl”,

“substituted or unsubstituted 6-membered aromatic carbocyclyl”, “substituted or unsubstituted 3- to 6-membered non-aromatic carbocyclyl”, “substituted or unsubstituted 5- to 6-membered aromatic heterocyclyl”, and “substituted or unsubstituted 5- to 6-membered non-aromatic heterocyclyl”,

“substituted or unsubstituted aromatic carbocyclyl”, “substituted or unsubstituted non-aromatic carbocyclyl”, “substituted or unsubstituted aromatic heterocyclyl”, and “substituted or unsubstituted non-aromatic heterocyclyl”,

“substituted or unsubstituted aromatic carbocyclyloxy”, “substituted or unsubstituted non-aromatic carbocyclyloxy”, “substituted or unsubstituted aromatic heterocyclyloxy”, and “substituted or unsubstituted non-aromatic heterocyclyloxy”, “substituted or unsubstituted aromatic carbocyclylamino”, “substituted or unsubstituted non-aromatic carbocyclylamino”, “substituted or unsubstituted aromatic heterocyclylamino”, and “substituted or unsubstituted non-aromatic heterocyclylamino”,

“substituted or unsubstituted aromatic carbocyclylsulfanyl”, “substituted or unsubstituted non-aromatic carbocyclylsulfanyl”, “substituted or unsubstituted aromatic heterocyclylsulfanyl”, and “substituted or unsubstituted non-aromatic heterocyclyl sulfanyl”,

“substituted or unsubstituted aromatic carbocyclylcarbonyl”, “substituted or unsubstituted non-aromatic carbocyclylcarbonyl”, “substituted or unsubstituted aromatic heterocyclylcarbonyl”, and “substituted or unsubstituted non-aromatic heterocyclylcarbonyl”,

“substituted or unsubstituted aromatic carbocyclylsulfonyl”, “substituted or unsubstituted non-aromatic carbocyclylsulfonyl”, “substituted or unsubstituted aromatic heterocyclylsulfonyl”, and “substituted or unsubstituted non-aromatic heterocyclylsulfonyl”,

“substituted or unsubstituted aromatic carbocyclylcarbonyloxy”, “substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy”, “substituted or unsubstituted aromatic heterocyclylcarbonyloxy”, and “substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy”,

“substituted or unsubstituted aromatic carbocyclyloxycarbonyl”, “substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl”, “substituted or unsubstituted aromatic heterocyclyloxycarbonyl”, and “substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl”,

“substituted or unsubstituted aromatic carbocyclylsulfonyloxy”, “substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy”, “substituted or unsubstituted aromatic heterocyclylsulfonyloxy”, and “substituted or unsubstituted non-aromatic haterocyclylsulfonyloxy”,

“substituted or unsubstituted aromatic carbocyclyloxysulfonyl”, “substituted or unsubstituted non-aromatic carbocyclyloxy sulfonyl”, “substituted or unsubstituted aromatic heterocyclyloxysulfonyl”, and “substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl”,

“substituted or unsubstituted aromatic carbocyclylcarbamoyl”, “substituted or unsubstituted non-aromatic carbocyclylcarbamoyl”, “substituted or unsubstituted aromatic heterocyclylcarbamoyl”, and “substituted or unsubstituted non-aromatic heterocyclylcarbamoyl”,

“substituted or unsubstituted aromatic carbocyclylsulfamoyl”, “substituted or unsubstituted non-aromatic carbocyclylsulfamoyl”, “substituted or unsubstituted aromatic heterocyclylsulfamoyl”, and “substituted or unsubstituted non-aromatic heterocyclylsulfamoyl”,

“substituted or unsubstituted aromatic carbocyclylcarbonylamino”, “substituted or unsubstituted non-aromatic carbocyclylcarbonylamino”, “substituted or unsubstituted aromatic heterocyclylcarbonylamino”, and “substituted or unsubstituted non-aromatic heterocyclylcarbonylamino”,

“substituted or unsubstituted aromatic carbocyclylsulfonylamino”, “substituted or unsubstituted non-aromatic carbocyclylsulfonylamino”, “substituted or unsubstituted aromatic heterocyclylsulfonylamino”, and “substituted or unsubstituted non-aromatic heterocyclylsulfonylamino”, and

“substituted or unsubstituted aromatic carbocyclyloxycarbonylamino”, “substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino”, “substituted or unsubstituted aromatic heterocyclyloxycarbonylamino”, and “substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino” include the substituent group D. An atom at any position(s) on the ring may be bonded to one or more group(s) selected from the substituent group G.

The substituent group C: halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkenyl optionally substituted with one or more group(s) selected from the substituent group D, alkynyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkenyloxy optionally substituted with one or more group(s) selected from the substituent, group D, alkynyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkenylamino optionally substituted with one or more group(s) selected from the substituent group D, alkynylamino optionally substituted with one or more group(s) selected from the substituent group U, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkenylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkynylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group D, aryloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyl optionally substituted with one or more group (s) selected from the substituent group E, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic, carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclyl amino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclyl sulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent, group E, non-aromatic heterocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent, group E, non-aromatic heterocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclyloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclyloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic, carbocyclyl sulfonyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyl sulfon yloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group E, and non-aromatic heterocyclylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group E.

The substituent group C: halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy, haloalkyloxy, alkylamino, haloalkylamino, alkylsulfanyl, haloalkylsulfanyl, and

aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent, group F, and non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F.

The substituent group D: halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, and cyano.

The substituent group E: halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, and cyano, and

alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group (a) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group D, and aryloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group D.

The substituent group F: halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl, haloalkyl, alkyloxy, haloaryloxy, alkylamino, haloalkylamino, alkylsulfanyl, haloalkylsulfanyl, alkylcarbonyl, haloalkylcarbonyl, alkylsulfonyl, haloalkylsulfonyl, alkylcarbonylamino, haloalkylcarbonylamino, alkylsulfonylamino, haloalkylsulfonylamino, alkylcarbamoyl, haloalkylcarbamoyl, alkylsulfamoyl, and haloalkylsulfamoyl.

“Substituted or unsubstituted non-aromatic carbocyclyl” and “substituted or unsubstituted non-aromatic heterocyclyl” may be optionally substituted with one or more group(s) selected from “oxo”. In this case, it means a group wherein two hydrogen atoms on a carbon atom are replaced as below.

The non-aromatic carbocycle or non-aromatic heterocycle part of the above “non-aromatic carbocyclyloxy”, “non-aromatic carbocyclylamino”, “non-aromatic carbocyclylsulfanyl”, “non-aromatic carbocyclylcarbonyl”, “non-aromatic carbocyclylsulfonyl”, “non-aromatic carbocyclylcarbonyloxy”, “non-aromatic carbocyclylsulfonyloxy”, “non-aromatic carbocyclyloxycarbonyl”, “non-aromatic carbocyclyloxysulfonyl”, “non-aromatic carbocyclylcarbamoyl”, “non-aromatic carbocyclylsulfamoyl”, “non-aromatic carbocyclylcarbonylamino”, “non-aromatic carbocyclylsulfonylamino”, “non-aromatic carbocyclyloxycarbonylamino”, “non-aromatic heterocyclyloxy”, “non-aromatic heterocyclylamino”, “non-aromatic heterocyclylsulfanyl”, “non-aromatic heterocyclyl carbonyl”, “non-aromatic heterocyclylsulfonyl”, “non-aromatic heterocyclylcarbonyloxy”, “non-aromatic heterocyclylsulfonyloxy”, “non-aromatic heterocyclyloxycarbonyl”, “non-aromatic heterocyclyloxysulfonyl”, “non aromatic heterocyclylcarbamoyl”, “non-aromatic heterocyclylsulfamoyl”, “non-aromatic heterocyclylcarbonylamino”, “non-aromatic heterocyclylsulfonylamino”, and “non-aromatic heterocyclyloxycarbonylamino” may be optionally substituted with one or more group(s) selected from “oxo” as above.

The substituents on the rings of “substituted or unsubstituted aromatic carbocyclyl”, “substituted or unsubstituted non-aromatic carbocyclyl”, “substituted or unsubstituted aromatic heterocyclyl”, “substituted or unsubstituted non-aromatic heterocyclyl”, “substituted or unsubstituted 5- to 10-membered aromatic carbocyclyl”, “substituted or unsubstituted 3- to 10-membered non-aromatic carbocyclyl”, “substituted or unsubstituted 5- to 10-membered aromatic heterocyclyl”, “substituted or unsubstituted 3- to 10-membered non-aromatic heterocyclyl”, “substituted or unsubstituted 6-membered aromatic carbocyclyl”, “substituted or unsubstituted 3- to 6-membered non-aromatic carbocyclyl”, “substituted or unsubstituted 5- to 6-membered aromatic heterocyclyl”, and “substituted or unsubstituted 5- to 6-membered non-aromatic heterocyclyl” in R 1 include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D and the like.

One embodiment, is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl, haloalkyl, alkyloxy, haloaryloxy, alkylamino, haloalkylamino, alkylsulfanyl, haloalkylsulfanyl, alkylcarbonyl, haloalkylcarbonyl, alkylsulfonyl, haloalkylsulfonyl, alkylcarbonylamino, haloalkylcarbonylamino, alkylsulfonylamino, haloalkylsulfonylamino, alkylcarbamoyl, haloalkylcarbamoyl, alkylsulfamoyl, haloalkylsulfamoyl, or the like.

One embodiment is, for example, halogen, hydroxy, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent, group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group Os) selected from the substituent group D or the like.

One embodiment is, for example, halogen, alkyl, haloalkyl, alkyloxy, haloaryloxy, alkylamino, haloalkylamino, alkylsulfanyl, haloalkylsulfanyl or the like.

One embodiment is, for example, halogen, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment is, for example, halogen, alkyl, haloalkyl, alkyloxy, haloalkyloxy or the like.

One embodiment is, for example, halogen, alkyl, haloalkyl or the like.

One embodiment is, for example, halogen.

One embodiment is, for example, halogen, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment is, for example, halogen, cyano, alkyl, haloalkyl, alkyloxy, haloalkyloxy or the like.

The substituents of “substituted or unsubstituted alkyl”, and “substituted or unsubstituted alkyloxy” in R 2a , R 2b , R 2c , R 2d , R 8a and R 8b include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano or the like.

One embodiment is, for example, halogen, hydroxy, cyano or the like.

One embodiment is, for example, halogen or the like.

The substituents of “substituted or unsubstituted alkyl”, and “substituted or unsubstituted alkylcarbonyl” in R 7a include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent, group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent, group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano or the like.

One embodiment is, for example, halogen, hydroxy, cyano or the like.

One embodiment is, for example, halogen or the like.

The substituents of “substituted or unsubstituted alkyl”, “substituted or unsubstituted alkenyl”, “substituted or unsubstituted alkynyl”, “substituted or unsubstituted alkyloxy”, “substituted or unsubstituted alkenyloxy”, “substituted or unsubstituted alkynyloxy”, “substituted or unsubstituted alkylsulfanyl”, “substituted or unsubstituted alkenylsulfanyl”, “substituted or unsubstituted alkynylsulfanyl”. “substituted or unsubstituted alkylamino”, “substituted or unsubstituted alkenylamino”, and “substituted or unsubstituted alkynylamino” in R 4 and R 6 include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent, group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano or the like.

One embodiment is, for example, halogen, hydroxy, cyano or the like.

One embodiment is, for example, halogen.

The substituents of “substituted or unsubstituted alkyl” in R 5a , R 5a′ and R 5b include halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group C, alkylamino optionally substituted with one or more group(s) selected from the substituent group C, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group C, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group C, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group C, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group C, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group C, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group C, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group C, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group E, non aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent, group E, aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent, group E, non-aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclyl amino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent, group E, non-aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclyl sulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfonyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic heterocyclylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent, group E, non-aromatic heterocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic carbocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, non-aromatic carbocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E, aromatic heterocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent, group E, non-aromatic heterocyclylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group E and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group C, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group C, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group C, aromatic carbocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent, group F, aromatic carbocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylcarbonyl amino optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclylcarbonyl amino optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, hydroxy, carboxy, carbamoyl, cyano, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group C, aromatic carbocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclylcarbonyl optionally substituted with one or more group(s) selected from the substituent, group F, aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylcarbamoyl optionally substituted with one or mom group(s) selected from the substituent group F, aromatic heterocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent-group F, non-aromatic heterocyclylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, hydroxy, carboxy, carbamoyl, alkylcarbamoyl optionally substituted with one or mom group(s) selected from (hydroxy, cyano and alkyloxy), non-aromatic heterocyclylcarbonyl, aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from (halogen and alkyl), non-aromatic heterocyclylcarbamoyl, or the like.

The substituents of “substituted or unsubstituted alkylcarbamoyl” in R 6a , R 5a′ and R 5b include halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or mom group(s) selected from the substituent, group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group F and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group (s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment, is, for example, halogen, hydroxy, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, cyano, alkyloxy, alkylcarbonyl, alkylsulfonyl, alkylcarbamoyl, aromatic carbocyclyl or the like.

The substituents of “substituted or unsubstituted alkenyl”, “substituted or unsubstituted alkynyl”, “substituted or unsubstituted alkyloxy”, “substituted or unsubstituted alkenyloxy”, “substituted or unsubstituted alkynyloxy”, “substituted or unsubstituted alkylsulfanyl”, “substituted or unsubstituted alkenylsulfanyl”, “substituted or unsubstituted alkynyl sulfanyl”, “substituted or unsubstituted alkylamino”, “substituted or unsubstituted alkenylamino”, “substituted or unsubstituted alkynylamino”, “substituted or unsubstituted alkylcarbonyl”, “substituted or unsubstituted alkenylcarbonyl”, “substituted or unsubstituted alkynylcarbonyl”, “substituted or unsubstituted alkylsulfonyl”, “substituted or unsubstituted alkenylsulfonyl”, “substituted or unsubstituted alkynylsulfinyl”, “substituted or unsubstituted alkylcarbonyloxy”, “substituted or unsubstituted alkenylcarbonyloxy”, “substituted or unsubstituted alkynylcarbonyloxy”, “substituted or unsubstituted alkyloxycarbonyl”, “substituted or unsubstituted alkenyloxycarbonyl”, “substituted or unsubstituted alkynyloxycarbonyl”, “substituted or unsubstituted alkylsulfonyloxy”, “substituted or unsubstituted alkenylsulfonyloxy”, “substituted or unsubstituted alkynylsulfonyloxy”, “substituted or unsubstituted alkyloxysulfonyl”, “substituted or unsubstituted alkenyloxysulfonyl”, “substituted or unsubstituted alkynyloxysulfonyl”, “substituted or unsubstituted alkylcarbamoyl”, “substituted or unsubstituted alkenylcarbamoyl”, “substituted or unsubstituted alkynylcarbamoyl”, “substituted or unsubstituted alkylsulfamoyl”, “substituted or unsubstituted alkenylsulfamoyl”, “substituted or unsubstituted alkynylsulfamoyl”, “substituted or unsubstituted alkylcarbonylamino”, “substituted or unsubstituted alkenylcarbonylamino”, “substituted or unsubstituted alkynylcarbonylamino”, “substituted or unsubstituted alkylsulfonylamino”, “substituted or unsubstituted alkenylsulfonylamino”, “substituted or unsubstituted alkyloxycarbonylamino”, “substituted or unsubstituted alkenyloxycarbonyl amino”, and “substituted or unsubstituted alkynyloxycarbonylamino” in R 5a , ligand R 5b include halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyloxy optionally substituted with one or more group (a) selected from the substituent group F, aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylsulfanyl optionally substituted with one or more group (s) selected from the substituent group F, aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclyl amino optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, and non-aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group F and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group (s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent, group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, hydroxy, cyano, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, aromatic carbocyclyl or the like.

One embodiment is, for example, halogen or the like.

The substituents of “substituted or unsubstituted alkyl”, “substituted or unsubstituted alkenyl”, “substituted or unsubstituted alkynyl”, “substituted or unsubstituted alkyloxy”, “substituted or unsubstituted alkenyloxy”, “substituted or unsubstituted alkynyloxy”, “substituted or unsubstituted alkylsulfanyl”, “substituted or unsubstituted alkenylsulfonyl”, “substituted or unsubstituted alkynyl sulfanyl”, “substituted or unsubstituted alkylamino”, “substituted or unsubstituted alkenylamino”, “substituted or unsubstituted alkynylamino”, “substituted or unsubstituted alkylcarbonyl”, “substituted or unsubstituted alkenylcarbonyl”, “substituted or unsubstituted alkynylcarbonyl”, “substituted or unsubstituted alkylsulfonyl”, “substituted or unsubstituted alkenylsulfonyl”, “substituted or unsubstituted alkynylsulfonyl”, “substituted or unsubstituted alkylcarbonyloxy”, “substituted or unsubstituted alkenylcarbonyloxy”, “substituted or unsubstituted alkynylcarbonyloxy”, “substituted or unsubstituted alkyloxycarbonyl”, “substituted or unsubstituted alkenyloxycarbonyl”, “substituted or unsubstituted alkynyloxycarbonyl”, “substituted or unsubstituted alkylsulfonyloxy”, “substituted or unsubstituted alkenylsulfonyloxy”, “substituted or unsubstituted alkynylsulfonyloxy”, “substituted or unsubstituted aryloxysulfonyl”, “substituted or unsubstituted alkenyloxysulfonyl”, “substituted or unsubstituted alkynyloxysulfonyl”, “substituted or unsubstituted alkylcarbamoyl”, “substituted or unsubstituted alkenylcarbamoyl”, “substituted or unsubstituted alkynylcarbamoyl”, “substituted or unsubstituted alkylsulfamoyl”, “substituted or unsubstituted alkenylsulfamoyl”, “substituted or unsubstituted alkynylsulfamoyl”, “substituted or unsubstituted alkylcarbonylamino”, “substituted or unsubstituted alkenylcarbonylamino”, “substituted or unsubstituted alkynylcarbonylamino”, “substituted or unsubstituted alkylsulfonylamino”, “substituted or unsubstituted alkenylsulfonylamino”, “substituted or unsubstituted alkyloxycarbonylamino”, “substituted or unsubstituted alkenyloxycarbonylamino”, and “substituted or unsubstituted alkynyloxycarbonylamino” in R 9a and R 9b include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group (a) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclyl sulfanyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent, group F, non-aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, and non-aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group F and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group (a) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, nonaromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent, group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, aromatic carbocyclyl, aromatic heterocyclyl or the like.

One embodiment is, for example, halogen or the like.

The substituents on the rings of “aromatic carbocycle”, “non-aromatic carbocycle”, “aromatic heterocycle”, and “non-aromatic heterocycle” of

“substituted or unsubstituted aromatic carbocyclyl”, “substituted or unsubstituted non-aromatic carbocyclyl”, “substituted or unsubstituted aromatic heterocyclyl”, and “substituted or unsubstituted non-aromatic heterocyclyl”.

“substituted or unsubstituted aromatic carbocyclyloxy”, “substituted or unsubstituted non-aromatic carbocyclyloxy”, “substituted or unsubstituted aromatic heterocyclyloxy”, and “substituted or unsubstituted non-aromatic heterocyclyloxy”, “substituted or unsubstituted aromatic carbocyclylamino”, “substituted or unsubstituted non-aromatic carbocyclylamino”, “substituted or unsubstituted aromatic heterocyclylamino”, and “substituted or unsubstituted non-aromatic heterocyclylamino”,

“substituted or unsubstituted aromatic carbocyclylsulfanyl”, “substituted or unsubstituted non-aromatic carbocyclylsulfanyl”, “substituted or unsubstituted aromatic heterocyclyl sulfanyl”, and “substituted or unsubstituted non-aromatic heterocyclylsulfanyl”,

“substituted or unsubstituted aromatic carbocyclylcarbonyl”, “substituted or unsubstituted non-aromatic carbocyclylcarbonyl”, “substituted or unsubstituted aromatic heterocyclylcarbonyl”, and “substituted or unsubstituted non-aromatic heterocyclylcarbonyl”,

“substituted or unsubstituted aromatic carbocyclylsulfonyl”, “substituted or unsubstituted non-aromatic carbocyclylsulfonyl”, “substituted or unsubstituted aromatic heterocyclylsulfanyl”, and “substituted or unsubstituted non-aromatic heterocyclylsulfonyl”,

“substituted or unsubstituted aromatic carbocyclylcarbonyloxy”, “substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy”, “substituted or unsubstituted aromatic heterocyclylcarbonyloxy”, and “substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy”,

“substituted or unsubstituted aromatic carbocyclyloxycarbonyl”, “substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl”, “substituted or unsubstituted aromatic heterocyclyloxycarbonyl”, and “substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl”,

“substituted or unsubstituted aromatic carbocyclylsulfonyloxy”, “substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy”, “substituted or unsubstituted aromatic heterocyclylsulfonyloxy”, and “substituted or unsubstituted non aromatic heterocyclylsulfonyloxy”,

“substituted or unsubstituted aromatic carbocyclyloxysulfonyl”, “substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl”, “substituted or unsubstituted aromatic heterocyclyloxysulfonyl”, and “substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl”,

“substituted or unsubstituted aromatic carbocyclylcarbamoyl”, “substituted or unsubstituted non-aromatic carbocyclylcarbamoyl”, “substituted or unsubstituted aromatic heterocyclylcarbamoyl”, and “substituted or unsubstituted non-aromatic heterocyclylcarbamoyl”,

“substituted or unsubstituted aromatic carbocyclylsulfamoyl”, “substituted or unsubstituted non-aromatic carbocyclylsulfamoyl”, “substituted or unsubstituted aromatic heterocyclylsulfamoyl”, and “substituted or unsubstituted non-aromatic heterocyclylsulfamoyl”,

“substituted or unsubstituted aromatic carbocyclylcarbonylamino”, “substituted or unsubstituted non-aromatic carbocyclylcarbonylamino”, “substituted or unsubstituted aromatic heterocyclylcarbonylamino”, and “substituted or unsubstituted non-aromatic heterocyclylcarbonylamino”,

“substituted or unsubstituted aromatic carbocyclylsulfonylamino”, “substituted or unsubstituted non-aromatic carbocyclylsulfonylamino”, “substituted or unsubstituted aromatic heterocyclylsulfonylamino”, and “substituted or unsubstituted non-aromatic heterocyclyl sulfonyl amino”, and

“substituted or unsubstituted aromatic carbocyclyloxycarbonylamino”, “substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino”, “substituted or unsubstituted aromatic heterocyclyloxycarbonylamino”, and “substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino” in R 9a and R 9b include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent, group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group (s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D and the like.

One embodiment is, for example, halogen, hydroxy, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment, is, for example, halogen, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment is, for example, halogen, alkyl, haloalkyl, alkyloxy, haloalkyloxy or the like.

One embodiment is, for example, halogen or the like.

The substituents of “substituted or unsubstituted alkyl”, “substituted or unsubstituted alkenyl”, “substituted or unsubstituted alkynyl”, “substituted or unsubstituted alkyloxy”, “substituted or unsubstituted alkenyloxy”, “substituted or unsubstituted alkynyloxy”, “substituted or unsubstituted alkylsulfanyl”, “substituted or unsubstituted alkenylsulfinyl”, “substituted or unsubstituted alkynylsulfanyl”. “substituted or unsubstituted alkylamino”, “substituted or unsubstituted alkenylamino”, “substituted or unsubstituted alkynylamino”, “substituted or unsubstituted alkylcarbonyl”, “substituted or unsubstituted alkenylcarbonyl”, “substituted or unsubstituted alkynylcarbonyl”, “substituted or unsubstituted alkylsulfonyl”, “substituted or unsubstituted alkenylsulfonyl”, “substituted or unsubstituted alkynylsulfinyl”, “substituted or unsubstituted alkylcarbonyloxy”, “substituted or unsubstituted alkenylcarbonyloxy”, “substituted or unsubstituted alkynylcarbonyloxy”, “substituted or unsubstituted alkyloxycarbonyl”, “substituted or unsubstituted alkenyloxycarbonyl”, “substituted or unsubstituted alkynyloxycarbonyl”, “substituted or unsubstituted alkylsulfonyloxy”, “substituted or unsubstituted alkenylsulfonyloxy”, “substituted or unsubstituted alkynylsulfonyloxy”, “substituted or unsubstituted aryloxysulfonyl”, “substituted or unsubstituted alkenyloxysulfonyl”, “substituted or unsubstituted alkynyloxysulfonyl”, “substituted or unsubstituted alkylcarbamoyl”, “substituted or unsubstituted alkenylcarbamoyl”, “substituted or unsubstituted alkynylcarbamoyl”, “substituted or unsubstituted alkylsulfamoyl”, “substituted or unsubstituted alkenylsulfamoyl”, “substituted or unsubstituted alkynylsulfamoyl”, “substituted or unsubstituted alkylcarbonylamino”, “substituted or unsubstituted alkenylcarbonylamino”, “substituted or unsubstituted alkynylcarbonylamino”, “substituted or unsubstituted alkylsulfonylamino”, “substituted or unsubstituted alkenylsulfonylamino”, “substituted or unsubstituted alkyloxycarbonylamino”, “substituted or unsubstituted alkenyloxycarbonylamino”, and “substituted or unsubstituted alkyloxycarbonylamino” in R 10a , R 10aa , R 10ab , R 10ac , R 10b , R 10c and R 10d include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent, group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, and non-aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group F and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent, group F, non-aromatic carbocyclyl optionally substituted with one or more group (s) selected from the substituent, group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent, group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment, is, for example, halogen, hydroxy, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent, group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, hydroxy, alkyloxy, haloalkyloxy, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent, group F or the like.

One embodiment is, for example, halogen, hydroxy, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, hydroxy, alkyloxy, haloalkyloxy, aromatic carbocyclyl, non-aromatic carbocyclyl, aromatic heterocyclyl, non-aromatic heterocyclyl or the like.

One embodiment is, for example, halogen, hydroxy, alkyloxy, non-aromatic heterocyclyl or the like.

One embodiment is, for example, halogen, hydroxy, alkyloxy or the like.

The substituents on the rings of “aromatic carbocycle”, “non-aromatic carbocycle”, “aromatic heterocycle”, and “non-aromatic heterocycle” of “substituted or unsubstituted aromatic carbocyclyl”, “substituted or unsubstituted non-aromatic carbocyclyl”, “substituted or unsubstituted aromatic heterocyclyl”, and “substituted or unsubstituted non-aromatic heterocyclyl”,

“substituted or unsubstituted aromatic carbocyclyloxy”, “substituted or unsubstituted non-aromatic carbocyclyloxy”, “substituted or unsubstituted aromatic heterocyclyloxy”, and “substituted or unsubstituted non-aromatic heterocyclyloxy”, “substituted or unsubstituted aromatic carbocyclylamino”, “substituted or unsubstituted non-aromatic carbocyclylamino”, “substituted or unsubstituted aromatic heterocyclylamino”, and “substituted or unsubstituted non-aromatic heterocyclylamino”,

“substituted or unsubstituted aromatic carbocyclylsulfanyl”, “substituted or unsubstituted non-aromatic carbocyclylsulfanyl”, “substituted or unsubstituted aromatic heterocyclyl sulfanyl”, and “substituted or unsubstituted non-aromatic heterocyclylsulfanyl”,

“substituted or unsubstituted aromatic carbocyclylcarbonyl”, “substituted or unsubstituted non-aromatic carbocyclylcarbonyl”, “substituted or unsubstituted aromatic heterocyclylcarbonyl”, and “substituted or unsubstituted non-aromatic heterocyclylcarbonyl”,

“substituted or unsubstituted aromatic carbocyclylsulfonyl”, “substituted or unsubstituted non-aromatic carbocyclylsulfonyl”, “substituted or unsubstituted aromatic heterocyclylsulfonyl”, and “substituted or unsubstituted non-aromatic heterocyclylsulfonyl”,

“substituted or unsubstituted aromatic carbocyclylcarbonyloxy”, “substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy”, “substituted or unsubstituted aromatic heterocyclylcarbonyloxy”, and “substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy”,

“substituted or unsubstituted aromatic carbocyclyloxycarbonyl”, “substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl”, “substituted or unsubstituted aromatic heterocyclyloxycarbonyl”, and “substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl”,

“substituted or unsubstituted aromatic carbocyclylsulfonyloxy”, “substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy”, “substituted or unsubstituted aromatic heterocyclylsulfonyloxy”, and “substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy”,

“substituted or unsubstituted aromatic carbocyclyloxysulfonyl”, “substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl”, “substituted or unsubstituted aromatic heterocyclyloxysulfonyl”, and “substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl”,

“substituted or unsubstituted aromatic carbocyclylcarbamoyl”, “substituted or unsubstituted non-aromatic carbocyclylcarbamoyl”, “substituted or unsubstituted aromatic heterocyenylcarbamoyl”, and “substituted or unsubstituted non-aromatic heterocyclylcarbamoyl”.

“substituted or unsubstituted aromatic carbocyclylsulfamoyl”, “substituted or unsubstituted non-aromatic carbocyclylsulfamoyl”, “substituted or unsubstituted aromatic heterocyclylsulfamoyl”, and “substituted or unsubstituted non-aromatic heterocyclylsulfamoyl”,

“substituted or unsubstituted aromatic carbocyclylcarbonylamino”, “substituted or unsubstituted non-aromatic carbocyclylcarbonylamino”, “substituted or unsubstituted aromatic heterocyclylcarbonylamino”, and “substituted or unsubstituted non-aromatic heterocyclylcarbonylamino”,

“substituted or unsubstituted aromatic carbocyclylsulfonylamino”, “substituted or unsubstituted non-aromatic carbocyclylsulfonylamino”, “substituted or unsubstituted aromatic heterocyclylsulfonylamino”, and “substituted or unsubstituted non-aromatic heterocyclylsulfonylamino”, and

“substituted or unsubstituted aromatic carbocyclyloxycarbonylamino”, “substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino”, “substituted or unsubstituted aromatic heterocyclyloxycarbonyl amino”, and “substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino” in R 10a , R 10aa , R 10ab , R 10ac , R 10b , R 10c and R 10d include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent, group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent, group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment is, for example, halogen, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment, is, for example, halogen, alkyl, haloalkyl, alkyloxy, haloalkyloxy or the like.

One embodiment is, for example, halogen, alkyl, haloalkyl or the like.

One embodiment is, for example, halogen, alkyl or the like.

The substituents of “substituted or unsubstituted alkyl”, and “substituted or unsubstituted alkyloxy” in R 10c include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano and the like.

One embodiment is, for example, halogen, hydroxy, cyano or the like.

One embodiment is, for example, halogen or the like.

The substituents on the rings of “substituted or unsubstituted aromatic carbocycle”, “substituted or unsubstituted non-aromatic carbocycle”, “substituted or unsubstituted aromatic heterocycle”, and “substituted or unsubstituted non-aromatic heterocycle” when

“R 9a and R 10a which an; attached to the adjacent atoms, or R 9b and R 10b which are attached to the adjacent atoms are taken together to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle”,

“R 11c is taken together with R 9a which is attached to the adjacent atom to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle”, and

“R 11c is taken together with R 9a which is attached to the adjacent atoms to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle,

and

the substituents on the rings of “substituted or unsubstituted 5-membered non-aromatic carbocycle”, “substituted or unsubstituted 5-membered aromatic heterocycle”, “substituted or unsubstituted 5-membered non-aromatic heterocycle”, “substituted or unsubstituted 6-membered aromatic carbocycle”, “substituted or unsubstituted 6-membered non-aromatic carbocycle”, “substituted or unsubstituted 6-membered aromatic heterocycle” and “substituted or unsubstituted 6-membered non-aromatic heterocycle” in Ring F3, Ring G3, and Ring H2 include,

for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylsulfonyloxy optionally substituted with one or more group(s) selected from the substituent group D, aryloxysulfonyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment is, for example, halogen, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment is, for example, halogen, alkyl, haloalkyl, alkyloxy, haloalkyloxy or the like.

One embodiment is, for example, halogen, alkyl or the like.

One embodiment is, for example, halogen, hydroxy, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, hydroxy, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxycarbonyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F or the like.

One embodiment is, for example, halogen, hydroxy, alkyl, alkyloxyoxycarbonyl, aromatic carbocyclyl or the like.

The substituents on the rings of “substituted or unsubstituted aromatic carbocycle”, “substituted or unsubstituted non-aromatic carbocycle”, “substituted or unsubstituted aromatic heterocycle”, and “substituted or unsubstituted non-aromatic heterocycle” when

“two R 10a which are attached to the adjacent atoms, or two R 10b which are attached to the adjacent atoms are taken together to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle”,

“R 11c is taken together with which is attached to the adjacent atom to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle”, and

“R 11d is taken together with R 11bb which is attached to the adjacent atoms to form a substituted or unsubstituted aromatic carbocycle, a substituted or unsubstituted non-aromatic carbocycle, a substituted or unsubstituted aromatic heterocycle, or a substituted or unsubstituted non-aromatic heterocycle”, and

the substituents on the rings of “substituted or unsubstituted 5-membered non-aromatic carbocycle”, “substituted or unsubstituted 5-membered aromatic heterocycle”, “substituted or unsubstituted 5-membered non-aromatic, heterocycle”, “substituted or unsubstituted 6-membered aromatic carbocycle”, “substituted or unsubstituted 6-membered non-aromatic carbocycle”, “substituted or unsubstituted 6-membered aromatic heterocycle” and “substituted or unsubstituted 6-membered non-aromatic heterocycle” in Ring F1, Ring F2, Ring G1, Ring G2, and Ring H1 include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally-substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent, group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment is, for example, halogen, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment is, for example, halogen, alkyl, haloalkyl, alkyloxy, haloalkyloxy or the like.

One embodiment is, for example, halogen, alkyl, haloalkyl, alkyloxy or the like.

The substituents of “substituted or unsubstituted alkyl”, “substituted or unsubstituted alkenyl”, “substituted or unsubstituted alkynyl”, “substituted or unsubstituted alkyloxy”, “substituted or unsubstituted alkenyloxy”, “substituted or unsubstituted alkynyloxy”, “substituted or unsubstituted alkylsulfanyl”, “substituted or unsubstituted alkenylsulfanyl”, “substituted or unsubstituted alkynyl sulfanyl”, “substituted or unsubstituted alkylamino”, “substituted or unsubstituted alkenylamino”, “substituted or unsubstituted alkynylamino”, “substituted or unsubstituted alkylcarbonyl”, “substituted or unsubstituted alkenylcarbonyl”, “substituted or unsubstituted alkynylcarbonyl”, “substituted or unsubstituted alkylsulfonyl”, “substituted or unsubstituted alkenylsulfonyl”, “substituted or unsubstituted alkynylsulfonyl”, “substituted or unsubstituted alkylcarbonyloxy”, “substituted or unsubstituted alkenylcarbonyloxy”, “substituted or unsubstituted alkynylcarbonyloxy”, “substituted or unsubstituted alkyloxycarbonyl”, “substituted or unsubstituted alkenyloxycarbonyl”, “substituted or unsubstituted alkynyloxycarbonyl”, “substituted or unsubstituted alkylsulfonyloxy”, “substituted or unsubstituted alkenylsulfonyloxy”, “substituted or unsubstituted alkynylsulfonyloxy”, “substituted or unsubstituted aryloxysulfonyl”, “substituted or unsubstituted alkenyloxysulfonyl”, “substituted or unsubstituted alkynyloxysulfonyl”, “substituted or unsubstituted alkylcarbamoyl”, “substituted or unsubstituted alkenylcarbamoyl”, “substituted or unsubstituted alkynylcarbamoyl”, “substituted or unsubstituted alkylsulfamoyl”, “substituted or unsubstituted alkenylsulfamoyl”, “substituted or unsubstituted alkynylsulfamoyl”, “substituted or unsubstituted alkylcarbonylamino”, “substituted or unsubstituted alkenylcarbonylamino”, “substituted or unsubstituted alkynylcarbonylamino”, “substituted or unsubstituted alkylsulfonylamino”, “substituted or unsubstituted alkenylsulfonylamino”, “substituted or unsubstituted alkyloxycarbonylamino”, “substituted or unsubstituted alkenyloxycarbonylamino”, and “substituted or unsubstituted alkynyloxycarbonylamino” in R 11a and R 11b include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent, group F, aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyloxy optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclylsulfanyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group F, and non-aromatic heterocyclylamino optionally substituted with one or more group(s) selected from the substituent group F and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent, group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent, group D or the like.

One embodiment is, for example, halogen, hydroxy, cyano or the like.

One embodiment is, for example, halogen or the like.

The substituents on the rings of “aromatic carbocycle”, “non-aromatic carbocycle”, “aromatic heterocycle”, and “non-aromatic heterocycle” of “substituted or unsubstituted aromatic carbocyclyl”, “substituted or unsubstituted non-aromatic carbocyclyl”, “substituted or unsubstituted aromatic heterocyclyl”, and “substituted or unsubstituted non-aromatic heterocyclyl”,

“substituted or unsubstituted aromatic carbocyclyloxy”, “substituted or unsubstituted non-aromatic carbocyclyloxy”, “substituted or unsubstituted aromatic, heterocyclyloxy”, and “substituted or unsubstituted non-aromatic, heterocyclyloxy”, “substituted or unsubstituted aromatic carbocyclylamino”, “substituted or unsubstituted non-aromatic carbocyclylamino”, “substituted or unsubstituted aromatic heterocyclylamino”, and “substituted or unsubstituted non-aromatic heterocyclylamino”,

“substituted or unsubstituted aromatic carbocyclylsulfanyl”, “substituted or unsubstituted non-aromatic carbocyclylsulfanyl”, “substituted or unsubstituted aromatic heterocyclylsulfanyl”, and “substituted or unsubstituted non-aromatic heterocyclylsulfanyl”,

“substituted or unsubstituted aromatic carbocyclylcarbonyl”, “substituted or unsubstituted non-aromatic carbocyclylcarbonyl”, “substituted or unsubstituted aromatic heterocyclylcarbonyl”, and “substituted or unsubstituted non-aromatic heterocyclylcarbonyl”,

“substituted or unsubstituted aromatic carbocyclylsulfonyl”, “substituted or unsubstituted non-aromatic carbocyclylsulfonyl”, “substituted or unsubstituted aromatic heterocyclylsulfonyl”, and “substituted or unsubstituted non-aromatic heterocyclylsulfonyl”,

“substituted or unsubstituted aromatic carbocyclylcarbonyloxy”, “substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy”, “substituted or unsubstituted aromatic heterocyclylcarbonyloxy”, and “substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy”,

“substituted or unsubstituted aromatic carbocyclyloxycarbonyl”, “substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl”, “substituted or unsubstituted aromatic heterocyclyloxycarbonyl”, and “substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl”,

“substituted or unsubstituted aromatic carbocyclylsulfonyloxy”, “substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy”, “substituted or unsubstituted aromatic heterocyclylsulfonyloxy”, and “substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy”,

“substituted or unsubstituted aromatic carbocyclyloxysulfonyl”, “substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl”, “substituted or unsubstituted aromatic heterocyclyloxysulfonyl”, and “substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl”.

“substituted or unsubstituted aromatic carbocyclylcarbamoyl”, “substituted or unsubstituted non-aromatic carbocyclylcarbamoyl”, “substituted or unsubstituted aromatic heterocyclylcarbamoyl”, and “substituted or unsubstituted non-aromatic heterocyclylcarbamoyl”,

“substituted or unsubstituted aromatic carbocyclylsulfamoyl”, “substituted or unsubstituted non-aromatic carbocyclylsulfamoyl”, “substituted or unsubstituted aromatic heterocycylsulfamoyl”, and “substituted or unsubstituted non-aromatic heterocyclylsulfamoyl”,

“substituted or unsubstituted aromatic carbocyclylcarbonylamino”, “substituted or unsubstituted non-aromatic carbocyclylcarbonylamino”, “substituted or unsubstituted aromatic heterocyclylcarbonylamino”, and “substituted or unsubstituted non-aromatic heterocyclylcarbonyl amino”,

“substituted or unsubstituted aromatic carbocyclylsulfonylamino”, “substituted or unsubstituted non-aromatic carbocyclylsulfonylamino”, “substituted or unsubstituted aromatic heterocyclylsulfonylamino”, and “substituted or unsubstituted non-aromatic heterocyclylsulfonylamino”, and

“substituted or unsubstituted aromatic carbocyclyloxycarbonyl amino”, “substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino”, “substituted or unsubstituted aromatic heterocyclyloxycarbonylamino”, and “substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino” in R 10a1 , R 10a2 , R 10b1 , R 11a and R 11b include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment is, for example, halogen, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment is, for example, halogen, alkyl, haloalkyl, alkyloxy, haloalkyloxy or the like.

One embodiment is, for example, halogen, alkyl, haloalkyl or the like.

One embodiment is, for example, halogen or the like.

The substituents of “substituted or unsubstituted alkyl”, “substituted or unsubstituted alkenyl”, “substituted or unsubstituted alkynyl”, “substituted or unsubstituted alkyloxy”, “substituted or unsubstituted alkenyloxy”, and “substituted or unsubstituted alkynyloxy” in R Y include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic carbocyclyl optionally substituted with one or more group(s) selected from the substituent group F, aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F, non-aromatic heterocyclyl optionally substituted with one or more group(s) selected from the substituent group F and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano or the like.

One embodiment, is, for example, halogen, hydroxy, cyano or the like.

One embodiment is, for example, halogen.

The substituents on the rings of “substituted or unsubstituted aromatic carbocyclyl”, “substituted or unsubstituted non-aromatic carbocyclyl”, “substituted or unsubstituted aromatic heterocyclyl”, and “substituted or unsubstituted non-aromatic heterocyclyl” in R Y include, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent, group D, alkylcarbonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonyl optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfonylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylcarbamoyl optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfamoyl optionally substituted with one or more group(s) selected from the substituent group D and the like.

One embodiment is, for example, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent, group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent group D or the like.

One embodiment is, for example, halogen, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent, group D or the like.

One embodiment is, for example, halogen, alkyl, haloalkyl, alkyloxy, haloalkyloxy or the like.

One embodiment is, for example, halogen, alkyl, haloalkyl or the like.

One embodiment, is, for example, halogen or the like.

One aspect of the present invention is illustrated below.

Specific examples of each substituent in the compound represented by Formula (I) or pharmaceutically acceptable salt thereof are shown below. All combinations of these specific examples are illustrated for the compound represented by Formula (I).

(a)

A compound according to any one of the following (a-1) to (a-3) or a pharmaceutically acceptable salt thereof.

(a-1) The compound represented by formula (I) wherein X is N(R 7a ) or O, or pharmaceutically acceptable salt thereof. (a-2) The compound represented by formula (I) wherein X is N(R 7a ), or pharmaceutically acceptable salt thereof. (a-3) The compound represented by formula (I) wherein X is O, or pharmaceutically acceptable salt thereof, (b) A compound according to any one of the following (b-1) to (b-3) or a pharmaceutically acceptable salt thereof. (b-1) The compound of formula (I) or the above (a), wherein R 7a is a hydrogen atom, or substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (b-2) The compound of formula (I) or the above (a), wherein R 7a is a hydrogen atom, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (b-3) The compound of formula (I) or the above (a), wherein R 7a is a hydrogen atom, or pharmaceutically acceptable salt thereof. (e) A compound according to any one of the following (c-1) to (c-4) or a pharmaceutically acceptable salt thereof. (c-1) The compound of formula (I) or the above (a) or (b), wherein R 8a and R 8b are each independently a hydrogen atom, halogen or substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (c-2) The compound of formula (I) or the above (a) or (b), wherein R 8a and R 8b are each independently a hydrogen atom, halogen, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (c-3) The compound of formula (I) or the above (a) or (b) wherein R 8a and R 8b are each independently a hydrogen atom, or halogen, or pharmaceutically acceptable salt thereof. (c-4) The compound of formula (I) or the above (a) or (b) wherein each of R 8a and R 8b is a hydrogen atom, or pharmaceutically acceptable salt thereof. (d) A compound according to any one of the following (d-1) to (d-7) or a pharmaceutically acceptable salt thereof. (d-1) The compound of any one of formula (I) and the above (a) to (c), wherein

or pharmaceutically acceptable salt thereof.

(d-2) The compound of any one of formula (I) and the above (a) to (c), wherein

or pharmaceutically acceptable salt thereof.

(d-3) The compound of any one of formula (I) and the above (a) to (c), wherein

or pharmaceutically acceptable salt thereof.

(d-4) The compound of any one of formula (I) and the above (a) to (c), wherein

or pharmaceutically acceptable salt thereof.

(d-5) The compound of any one of formula (I) and the above (a) to (c), wherein

or pharmaceutically acceptable salt thereof.

(d-6) The compound of any one of formula (I) and the above (a) to (c), wherein

or pharmaceutically acceptable salt thereof.

(d-7) The compound of any one of formula (I) and the above (a) to (c), wherein

or pharmaceutically acceptable salt thereof.

(e) A compound according to any one of the following (e-1) to (e-37) or a pharmaceutically acceptable salt thereof. (e-1) The compound of any one of formula (I) and the above (a) to (d), wherein R 1 is substituted or unsubstituted 6- to 10-membered aromatic carbocyclyl, substituted or unsubstituted 3- to 10-membered non-aromatic carbocyclyl, substituted or unsubstituted 5- to 10-membered aromatic heterocyclyl, or substituted or unsubstituted 3- to 10-membered non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (e-2) The compound of any one of formula (I) and the above (a) to (d), wherein R 1 is substituted or unsubstituted 6-membered aromatic carbocyclyl, substituted or unsubstituted 3- to 6-membered non-aromatic carbocyclyl, substituted or unsubstituted 5- to 6-membered aromatic heterocyclyl, or substituted or unsubstituted 5- to 6-membered non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (e-3) The compound of any one of formula (I) and the above (a) to (d), wherein R 1 is substituted or unsubstituted 6-membered aromatic carbocyclyl, or substituted or unsubstituted 5- to 6-membered aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (e-4) The compound of any one of formula (I) and the above (a) to (d), wherein R 1 is substituted or unsubstituted phenyl, or substituted or unsubstituted thienyl, or pharmaceutically acceptable salt thereof. (e-5) The compound of any one of formula (I) and the above (a) to (d), wherein R 1 is 6-membered aromatic carbocyclyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s), 3- to 6-membered non-aromatic carbocyclyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s), 5- to 6-membered aromatic heterocyclyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s), or 5- to 6-membered non-aromatic heterocyclyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s), or pharmaceutically acceptable salt thereof. (e-6) The compound of any one of formula (I) and the above (a) to (d), wherein R 1 is 6-membered aromatic carbocyclyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s), or 5′ to 6-membered aromatic heterocyclyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s), or pharmaceutically acceptable salt thereof. (e-7) The compound of any one of formula (I) and the above (a) to (d), wherein R 1 is phenyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s), or thienyl substituted with one or more halogen atom(s) and optionally substituted with one or more and same or different substituent(s), or pharmaceutically acceptable salt thereof. (e-8) The compound of any one of formula (I) and the above (a) to (d), wherein R 1 is phenyl substituted with one or more halogen atom(s) and optionally substituted with one or more group(s) selected from halogen, alkyl, haloalkyl, alkyloxy, and haloaryloxy, or thienyl substituted with one or more halogen atom(s) and optionally substituted with one or more group(s) selected from halogen, alkyl, haloalkyl, alkyloxy, and haloaryloxy, or pharmaceutically acceptable salt thereof. (e-9) The compound of any one of formula (I) and the above (a) to (d), wherein R 1 is phenyl substituted with one or more halogen atom(s) and optionally substituted with one or more group(s) selected from halogen, alkyl, and haloalkyl, or pharmaceutically acceptable salt thereof. (e-10) The compound of any one of formula (I) and the above (a) to (d), wherein R 1 is a group represented by the formula:

wherein

Ring E is a 6-membered aromatic carbocycle, a 6-membered non-aromatic carbocycle, a 6-membered aromatic heterocycle, or a 6-membered non-aromatic heterocycle; Ring F is a 5-membered non-aromatic carbocycle, a 5-membered aromatic heterocycle, or a 5-membered non-aromatic heterocycle; R 12a , R 13a , and R 14a are each independently halogen; R 12 , R 13 , and R 14 are each independently a group selected from the substituent group C; q1 is an integer from 0 to 2; q2 is an integer from 0 to 2; and q3 is 0 or 1,

or pharmaceutically acceptable salt thereof.

(e-11) The compound of any one of formula (I) and the above (a) to (d), wherein R 1 is a group represented by the formula:

wherein

R 12 and R 13 are each independently a group selected from the substituent group C; R 12a and R 13a are each independently halogen; R 12b and R 13b are each independently halogen, alkyl optionally substituted with one or more group(s) selected from the substituent group D, or alkyloxy optionally substituted with one or more group(s) selected from the substituent group D; q1a is 0 or 1; and q2a is 0 or 1,

or pharmaceutically acceptable salt thereof.

(e-12) The compound of any one of formula (I) and the above (a) to (d), wherein R 1 is a group represented by the formula:

wherein

R 12a and R 13a are each independently halogen; and

each of R 12b , R 12e , and R 13b is halogen, alkyl optionally substituted with one or more group(s) selected from the substituent group D, or alkyloxy optionally substituted with one or more group(s) selected from the substituent group D,

or pharmaceutically acceptable salt thereof.

(e-13) The compound of any one of the above (e-10) to (e-12), wherein R 12a , R 13a and R 14a are each independently a fluorine atom, or a chlorine atom, or pharmaceutically acceptable salt thereof. (e-14) The compound of any one of the above (e-10) to (e-12), wherein each of R 12a , R 13a and R 14a is a fluorine atom, or pharmaceutically acceptable salt thereof. (e-15) The compound of any one of the above (e-10) to (e-14), wherein R 12b , R 12c and R 13b are each independently halogen, or alkyl optionally substituted with one or more group(s) selected from the substituent group D, or pharmaceutically acceptable salt thereof. (e-16) The compound of any one of the above (e-10) to (e-14), wherein R 12b , R 12c and R 13b are each independently halogen, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (e-17) The compound of any one of the above (e-10) to (e-14), wherein R 12b , R 12c and R 31b are each independently halogen, methyl, or halomethyl, or pharmaceutically acceptable salt thereof. (e-18) The compound of any one of the above (e-10) to (e-14), wherein R 12b , R 12c and R 13b are each independently a fluorine atom, or a chlorine atom, or pharmaceutically acceptable salt thereof. (e-19) The compound of any one of the above (e-10) to (e-14), wherein each of R 12b , R 12c anil R 13b is a fluorine atom, or pharmaceutically acceptable salt thereof. (e-20) The compound of any one of the above (e-10) to (e-19), wherein R 12 , R 13 , and R 14 are each independently halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, alkyloxy optionally substituted with one or more group(s) selected from the substituent, group D, alkylamino optionally substituted with one or more group(s) selected from the substituent group D, or alkylsulfanyl optionally substituted with one or more group(s) selected from the substituent, group D, or pharmaceutically acceptable salt thereof. (e-21) The compound of any one of the above (e-10) to (e-19), wherein R 12 , R 13 , and R 14 are each independently halogen, cyano, alkyl optionally substituted with one or more group(s) selected from the substituent group D, or alkyloxy optionally substituted with one or more group(s) selected from the substituent group D, or pharmaceutically acceptable salt thereof. (e-22) The compound of any one of the above (e-10) to (e-19), wherein R 12 , R 13 , and R 14 are each independently halogen, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (e-23) The compound of any one of the above (e-10) to (e-19), wherein R 12 , R 13 , and R 14 are each independently halogen, methyl, or halomethyl, or pharmaceutically acceptable salt thereof. (e-24) The compound of any one of the above (e-10) to (e-19), wherein R 12 , R 13 , and R 14 are each independently a fluorine atom, or a chlorine atom, or pharmaceutically acceptable salt thereof. (e-25) The compound of any one of the above (e-10) to (e-19), wherein each of R 12 , R 13 , and R 14 is a fluorine atom, or pharmaceutically acceptable salt thereof. (e-26) The compound of any one of the above (e-10) to (e-25), wherein each of q1, q2, and q3 is 0, or pharmaceutically acceptable salt thereof. (e-27) The compound of any one of the above (e-10) to (e-25), wherein each of q1, q2, and q3 is 1, or pharmaceutically acceptable salt thereof. (e-28) The compound of any one of the above (e-10) to (e-25), wherein each of q1 and q2 is 2, or pharmaceutically acceptable salt, thereof. (e-29) The compound of any one of the above (e-10) to (e-25), wherein each of q1a and q2a is 0, or pharmaceutically acceptable salt thereof. (e-30) The compound of any one of the above (e-10) to (e-25), wherein each of q1a and q2a is 1, or pharmaceutically acceptable salt thereof. (e-31) The compound of any one of the above (e-10) to (e-30), wherein Ring E is cyclohexene, benzene or a 0-membered aromatic heterocycle, or pharmaceutically acceptable salt thereof. (e-32) The compound of any one of the above (e-10) to (e-30), wherein Ring E is benzene, or a 6-membered aromatic heterocycle, or pharmaceutically acceptable salt thereof. (e-33) The compound of any one of the above (e-10) to (e-30), wherein Ring E is benzene, pyridine, pyrimidine, or pyrazine, or pharmaceutically acceptable salt thereof. (e-31) The compound of any one of the above (e-10) to (e-30), wherein Ring E is benzene, or pyridine, or pharmaceutically acceptable salt thereof. (e-35) The compound of any one of the above (e-10) to (e-30), wherein Ring E is benzene, or pharmaceutically acceptable salt thereof. (e-36) The compound of any one of the above (e-10) to (e-35), wherein Ring F is a 5-membered aromatic heterocycle, or pharmaceutically acceptable salt thereof. (e-37) The compound of any one of the above (e-10) to (e-35), wherein Ring F is thiophene, or pharmaceutically acceptable salt thereof. (f) A compound according to any one of the following (f-1) to (f-21) or a pharmaceutically acceptable salt thereof. (f-1) The compound of any one of formula (I) and the above (a) to (e), wherein R 8 is a group represented by the Formula:

wherein

R 9a and R 9b are each independently halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfonyl, substituted or unsubstituted alkylcarbonyloxy, substituted or unsubstituted alkenylcarbonyloxy, substituted or unsubstituted alkynylcarbonyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylsulfonyloxy, substituted or unsubstituted alkenylsulfonyloxy, substituted or unsubstituted alkynylsulfonyloxy, substituted or unsubstituted aryloxysulfonyl, substituted or unsubstituted alkenyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylsulfamoyl, substituted or unsubstituted alkenylsulfamoyl, substituted or unsubstituted alkynylsulfamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkylsulfonylamino, substituted or unsubstituted alkenylsulfonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylcarbonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic heterocyclylcarbonyloxy, substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy, substituted or unsubstituted aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy, substituted or unsubstituted aromatic carbocyclyloxysulfonyl, substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl, substituted or unsubstituted aromatic heterocyclyloxysulfonyl, substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, substituted or unsubstituted non-aromatic heterocyclylsulfamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonylamino, substituted or unsubstituted aromatic heterocyclylcarbonyl amino, substituted or unsubstituted non-aromatic heterocyclylcarbonylamino, substituted or unsubstituted aromatic carbocyclylsulfonylamino, substituted or unsubstituted non-aromatic carbocyclylsulfonylamino, substituted or unsubstituted aromatic heterocyclylsulfonylamino, substituted or unsubstituted non-aromatic heterocyclylsulfonylamino, substituted or unsubstituted aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted aromatic heterocyclyloxycarbonylamino, or substituted or unsubstituted non-aromatic heterocyclyloxy carbonylamino:

R 10a and R 10b are each independently halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfinyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfonyl, substituted or unsubstituted alkylcarbonyloxy, substituted or unsubstituted alkenylcarbonyloxy, substituted or unsubstituted alkynylcarbonyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylsulfonyloxy, substituted or unsubstituted alkenylsulfonyloxy, substituted or unsubstituted alkynylsulfonyloxy, substituted or unsubstituted aryloxysulfonyl, substituted or unsubstituted alkenyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylsulfamoyl, substituted or unsubstituted alkenylsulfamoyl, substituted or unsubstituted alkynylsulfamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkylsulfonylamino, substituted or unsubstituted alkenylsulfonylamino, substituted or unsubstituted alkynylsulfonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclyl amino, substituted or unsubstituted non-aromatic carbocyclylmino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclyl sulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclyl sulfonyl, substituted or unsubstituted aromatic heterocyclyl sulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylcarbonyloxy, substituted or unsubstituted non-aromatic carbocyclylcarbonyloxy, substituted or unsubstituted aromatic heterocyclylcarbonyloxy, substituted or unsubstituted non-aromatic heterocyclylcarbonyloxy, substituted or unsubstituted aromatic carbocyclyloxycarbonyl, substituted or unsubstituted non-aromatic carbocyclyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyloxycarbonyl, substituted or unsubstituted non-aromatic heterocyclyloxycarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyloxy, substituted or unsubstituted non-aromatic carbocyclylsulfonyloxy, substituted or unsubstituted aromatic heterocyclylsulfonyloxy, substituted or unsubstituted non-aromatic heterocyclylsulfonyloxy, substituted or unsubstituted aromatic carbocyclyloxysulfonyl, substituted or unsubstituted non-aromatic carbocyclyloxysulfonyl, substituted or unsubstituted aromatic heterocyclyloxysulfonyl, substituted or unsubstituted non-aromatic heterocyclyloxysulfonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, substituted or unsubstituted non-aromatic heterocyclylsulfamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonyl amino, substituted or unsubstituted aromatic heterocyclylcarbonyl amino, substituted or unsubstituted non-aromatic heterocyclylcarbonylamino, substituted or unsubstituted aromatic carbocyclylsulfonylamino, substituted or unsubstituted non-aromatic carbocyclylsulfonylamino, substituted or unsubstituted aromatic heterocyclylsulfonylamino, substituted or unsubstituted non-aromatic heterocyclylsulfonylamino, substituted or unsubstituted aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted non-aromatic carbocyclyloxycarbonylamino, substituted or unsubstituted aromatic heterocyclyloxycarbonylamino, or substituted or unsubstituted non-aromatic heterocyclyloxycarbonylamino:

p1 is an integer from 0 to 3; and p2 is an integer from 0 to 2,

or pharmaceutically acceptable salt thereof.

(f-2) The compound of the above (f-1), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(f-3) The compound of the above (f-1), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(f-4) The compound of any one of the above (f-1) to (f-3), wherein R 10a and R 10b are each independently halogen, hydroxy, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynyl sulfonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted aryloxysulfonyl, substituted or unsubstituted alkenyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, or substituted or unsubstituted non-aromatic heterocyclylsulfanyl, or pharmaceutically acceptable salt thereof. (f-5) The compound of any one of the above (f-1) to (f-3), wherein R 10a and R 10b are each independently halogen, hydroxy, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted aryloxysulfonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic, carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, or substituted or unsubstituted non-aromatic heterocyclylsulfanyl, or pharmaceutically acceptable salt thereof. (f-6) The compound of any one of the above (f-1) to (f-3), wherein R 10a and R 10b are each independently halogen, hydroxy, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted aryloxysulfonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (f-7) The compound of any one of the above (f-1) to (f-3), wherein R 10a and R 10b are each independently halogen, hydroxy, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, or substituted or unsubstituted aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (f-8) The compound of any one of the above (f-1) to (f-3), wherein R 10a and R 10b are each independently halogen; hydroxy; carbamoyl; cyano; alkyl substituted with one or more group(s) selected from halogen, hydroxy, alkyloxy, and a non-aromatic heterocycle; unsubstituted alkyl; alkenyl substituted with one or more group(s) selected from halogen, hydroxy, alkyloxy, and a non-aromatic heterocycle; unsubstituted alkenyl; alkynyl substituted with one or more group(s) selected from halogen, hydroxy, alkyloxy, and a non-aromatic heterocycle; unsubstituted alkynyl; alkyloxy substituted with one or more group(s) selected from halogen, hydroxy, alkyloxy, and a non-aromatic heterocycle; unsubstituted alkyloxy; alkylsulfanyl substituted with one or more group(s) selected from halogen, hydroxy, alkyloxy, and a non-aromatic heterocycle; unsubstituted alkylsulfanyl; alkylamino substituted with one or more group(s) selected from halogen, hydroxy, alkyloxy, and a non-aromatic heterocyclo; unsubstituted alkylamino; alkylcarbonyl substituted with one or more group(s) selected from halogen, hydroxy, alkyloxy, and a non-aromatic heterocycle; unsubstituted alkylcarbonyl; alkylsulfonyl substituted with one or more group(s) selected from halogen, hydroxy, alkyloxy, and a non-aromatic heterocycle; unsubstituted alkylsulfonyl; alkyloxycarbonyl substituted with one or more group(s) selected from halogen, hydroxy, alkyloxy, and a non-aromatic heterocycle; unsubstituted alkyloxycarbonyl; aromatic heterocyclyl substituted with one or more group(s) selected from halogen, alkyl, alkyloxy, and alkyloxycarbonyl; unsubstituted aromatic heterocyclyl; non-aromatic heterocyclyl substituted with one or more group(s) selected from halogen, alkyl, alkyloxy, and alkyloxycarbonyl; unsubstituted non-aromatic heterocyclyl; aromatic carbocyclyloxy substituted with one or more group(s) selected from halogen, alkyl, alkyloxy, and alkyloxycarbonyl; unsubstituted aromatic carbocyclyloxy; aromatic heterocyclyloxy substituted with one or more group(s) selected from halogen, alkyl, alkyloxy, and alkyloxycarbonyl; or unsubstituted aromatic heterocyclyloxy,

or pharmaceutically acceptable salt thereof.

(f-9) The compound of any one of the above (f-1) to (f-3), wherein R 10a and R 10b are each independently halogen; hydroxy; carbamoyl; cyano; alkyl substituted with one or more group(s) selected from halogen, hydroxy, alkyloxy, and a non-aromatic heterocycle; unsubstituted alkyl; unsubstituted alkenyl; unsubstituted alkynyl; alkyloxy substituted with one or more group(s) selected from halogen; unsubstituted alkyloxy; alkylsulfanyl substituted with one or more group(s) selected from halogen; unsubstituted alkylsulfanyl; unsubstituted alkylamino; unsubstituted alkylcarbonyl; unsubstituted alkylsulfonyl; unsubstituted alkyloxycarbonyl; aromatic heterocyclyl substituted with one or more group(s) selected from alkyl and alkyloxy; unsubstituted aromatic heterocyclyl; non-aromatic heterocyclyl substituted with one or more group(s) selected from alkyl and alkyloxycarbonyl; unsubstituted non-aromatic heterocyclyl; unsubstituted aromatic carbocyclyloxy; aromatic heterocyclyloxy substituted with one or more group(s) selected from halogen; or unsubstituted aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (f10) The compound of any one of the above (f-1) to (f-3), wherein R 10a and R 10b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (f-11) The compound of any one of the above (f-1) to (f-3), wherein R 10a and R 10b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, or substituted or unsubstituted non-aromatic heterocyclyl sulfanyl, or pharmaceutically acceptable salt thereof. (f-12) The compound of any one of the above (f-1) to (f-3), wherein R 10a and R 10b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted noil-aromatic heterocyclyl, substituted or unsubstituted aromatic carboey cl yloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (f-13) The compound of any one of the above (f-1) to (f-3), wherein R 10a and R 0b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic heterocyclylsulfanyl, or substituted or unsubstituted non-aromatic heterocyclylsulfanyl, or pharmaceutically acceptable salt thereof. (f-14) The compound of any one of the above (f-1) to (f-3), wherein R 10a and R 10b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (f-15) The compound of any one of the above (f-1) to (f-3), wherein R 10a and R 10b are each independently halogen; alkyl; haloalkyl; alkyloxy; haloalkyloxy; aromatic heterocyclyl substituted with one or more group(s) selected from halogen, alkyl, haloalkyl, alkyloxy, and haloalkyloxy; unsubstituted aromatic heterocyclyl; non-aromatic heterocyclyl substituted with one or more group(s) selected from halogen, alkyl, haloalkyl, alkyloxy, and haloalkyloxy; unsubstituted non-aromatic heterocyclyl; aromatic heterocyclyloxy substituted with one or more group(s) selected from halogen, alkyl, haloalkyl, alkyloxy, and haloalkyloxy; or unsubstituted aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (f-16) The compound of any one of the above (f-1) to (f-1.5), wherein p1 is 1 or 2, or pharmaceutically acceptable salt thereof. (f-17) The compound of any one of the above (f-1) to (f-15), wherein p1 is 2, or pharmaceutically acceptable salt thereof. (f-18) The compound of any one of the above (f-1) to (f-15), wherein p1 is 1, or pharmaceutically acceptable salt thereof. (f-19) The compound of any one of the above (f-1) to (f-1.5), wherein p1 is 0, or pharmaceutically acceptable salt thereof. (f-20) The compound of any one of the above (f-1) to (f-9), wherein p2 is 1, or pharmaceutically acceptable salt thereof. (f-21) The compound of any one of the above (f-1) to (f-19), wherein p2 is 0, or pharmaceutically acceptable salt thereof. (g) A compound according to any one of the following (g-1) to (g-51) or a pharmaceutically acceptable salt thereof. (g-1) The compound of any one of Formula (I) and the above (a) to (f), wherein R 3 is a group represented by the Formula:

wherein R 10aa , R 10ab , and R 10ac are each independently the same as R 10a of the above (f-1),

or pharmaceutically acceptable salt thereof.

(g-2) The compound of any one of Formula (I) and the above (a) to (f), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(g-3) The compound of any one of Formula (I) and the above (a) to (f), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(g-4) The compound of any one of Formula (I) and the above (a) to (f), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(g-5) The compound of any one of Formula (I) and the above (a) to (f), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(g-6) The compound of any one of Formula (I) and the above (a) to (f), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(g-7) The compound of any one of Formula (I) and the above (a) to (f), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(g-8) The compound of any one of Formula (I) and the above (a) to (f), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(g-9) The compound of any one of Formula (I) and the above (a) to (f), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(g-10) The compound of any one of the above (g-1) to (g-9), wherein R 10aa is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (g-11) The compound of any one of the above (g-1) to (g-9), wherein R 10aa is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (g-12) The compound of any one of the above (g-1) to (g-9), wherein R 10aa is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted aromatic carbocyclyloxy, or pharmaceutically acceptable salt thereof. (g-13) The compound of any one of the above (g-1) to (g-9), wherein R 10aa is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, or substituted or unsubstituted alkynylamino, or pharmaceutically acceptable salt thereof. (g-14) The compound of any one of the above (g-1) to (g-9), wherein R 10aa is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, or substituted or unsubstituted alkylamino, or pharmaceutically acceptable salt thereof. (g-15) The compound of any one of the above (g-1) to (g-9), wherein R 10aa is halogen, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy, or pharmaceutically acceptable salt thereof. (g-16) The compound of any one of the above (g-1) to (g-9), wherein R 10aa is halogen, alkyl, haloalkyl, alkyloxy, or haloalkyloxy, or pharmaceutically acceptable salt thereof. (g-17) The compound of any one of the above (g-1) to (g-9), wherein R 10aa is alkyl substituted with one or more group (s) selected from halogen, hydroxy, and alkyloxy; unsubstituted alkyl; alkyloxy substituted with one or more group(s) selected from halogen, hydroxy, and alkyloxy; unsubstituted alkyloxy; alkylamino substituted with one or more group(s) selected from halogen, hydroxy, and alkyloxy; unsubstituted alkylamino; alkylsulfanyl substituted with one or more group(s) selected from halogen, hydroxy, and alkyloxy; unsubstituted alkylsulfanyl; alkyloxycarbonyl substituted with one or more group(s) selected from halogen, hydroxy, and alkyloxy; unsubstituted alkyloxycarbonyl; unsubstituted aromatic heterocyclyl; or unsubstituted aromatic carbocyclyloxy, or pharmaceutically acceptable salt thereof. (g-18) The compound of any one of the above (g-1) to (g-9), wherein R 10aa is alkyl substituted with one or more group(s) selected from halogen, hydroxy, and alkyloxy; unsubstituted alkyl; alkyloxy substituted with one or more group(s) selected from halogen; unsubstituted alkyloxy: unsubstituted alkylamino; unsubstituted alkylsulfanyl; unsubstituted alkyloxycarbonyl; unsubstituted aromatic heterocyclyl; or unsubstituted aromatic carbocyclyloxy,

or pharmaceutically acceptable salt thereof.

(g-19) The compound of any one of the above (g-1) to (g-9), wherein R 10aa is halogen, or pharmaceutically acceptable salt thereof. (g-20) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is halogen, hydroxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt, thereof. (g-21) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is halogen, hydroxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (g-22) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is halogen, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted non-aromatic heterocyclyl, or substituted or unsubstituted aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (g-23) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is halogen, hydroxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, or substituted or unsubstituted alkynylamino, or pharmaceutically acceptable salt thereof. (g-24) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, or substituted or unsubstituted alkylamino, or pharmaceutically acceptable salt thereof. (g-25) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is halogen, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy, or pharmaceutically acceptable salt, thereof. (g-26) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is halogen, alkyl, haloalkyl, alkyloxy, or haloalkyloxy, or pharmaceutically acceptable salt thereof. (g-27) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is halogen; cyano; alkyl substituted with one or more group(s) selected from halogen; unsubstituted alkyl; alkyloxy substituted with one or more group(s) selected from halogen; unsubstituted alkyloxy; alkylamino substituted with one or more group(s) selected from halogen; unsubstituted alkyloxy; non-aromatic heterocyclyl substituted with one or more group(s) selected from halogen; unsubstituted non-aromatic heterocyclyl; aromatic heterocyclyloxy substituted with one or more group(s) selected from halogen; or unsubstituted aromatic heterocyclyloxy,

or pharmaceutically acceptable salt thereof.

(g-28) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is halogen; cyano; unsubstituted alkyl; alkyloxy substituted with one or more groups(s) selected from halogen; unsubstituted alkyloxy; unsubstituted alkylamino; unsubstituted non-aromatic heterocyclyl; or aromatic heterocyclyloxy substituted with one or more group(s) selected from halogen,

or pharmaceutically acceptable salt thereof.

(g-29) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is halogen or pharmaceutically acceptable salt thereof. (g-30) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is a fluorine atom or a chlorine atom, or pharmaceutically acceptable salt thereof. (g-31) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (g-32) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is alkyl or haloalkyl, or pharmaceutically acceptable salt thereof. (g-33) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is substituted or unsubstituted alkyloxy, or pharmaceutically acceptable salt thereof. (g-34) The compound of any one of the above (g-1) to (g-19), wherein R 10ab is alkyloxy or haloalkyloxy, or pharmaceutically acceptable salt thereof. (g-35) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is halogen, hydroxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfinyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted aryloxysulfonyl, substituted or unsubstituted alkenyloxysulfonyl, substituted or unsubstituted alkynyloxysulfonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclyl amino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, or substituted or unsubstituted non-aromatic heterocyclyl sulfanyl, or pharmaceutically acceptable salt thereof. (g-36) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is halogen, hydroxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted aryloxysulfonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, or substituted or unsubstituted non-aromatic heterocyclylsulfanyl, or pharmaceutically acceptable salt thereof. (g-37) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is halogen, hydroxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkyloxysulfonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (g-38) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted non-aromatic carbocyclyloxy, or substituted or unsubstituted aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (g-39)

The compound of any one of the above (g-11 to (g-34), wherein R 10ac is alkyl substituted with one or more group(s) selected from halogen, hydroxy, and non-aromatic heterocyclyl; unsubstituted alkyl;

alkyl substituted with one or more group(s) selected from halogen, hydroxy, and non-aromatic heterocyclyl; unsubstituted alkenyl; alkyl substituted with one or more group(s) selected from halogen, hydroxy, and non-aromatic heterocyclyl; unsubstituted alkynyl: unsubstituted alkynyl; alkyloxy substituted with one or more group(s) selected from halogen, hydroxy, and non-aromatic heterocyclyl; unsubstituted alkyloxy: alkylsulfanyl substituted with one or more group(s) selected from halogen, hydroxy, and non-aromatic heterocyclyl; unsubstituted alkylsulfanyl; alkylsulfonyl substituted with one or more group(s) selected from halogen, hydroxy, and non-aromatic heterocyclyl; unsubstituted alkylsulfonyl: alkyloxycarbonyl substituted with one or more group(s) selected from halogen, hydroxy, and non-aromatic heterocyclyl; unsubstituted alkyloxycarbonyl; aromatic carbocyclyl substituted with one or more group (a) selected from alkyl, alkyloxy, and alkyloxycarbonyl; unsubstituted aromatic carbocyclyl: aromatic heterocyclyl substituted with one or more group(s) selected from alkyl, alkyloxy, and alkyloxycarbonyl; unsubstituted aromatic heterocyclyl; non-aromatic heterocyclyl substituted with one or more group(s) selected from alkyl, alkyloxy, and alkyloxycarbonyl; unsubstituted non-aromatic heterocyclyl; non-aromatic carbocyclyloxy substituted with one or more group(s) selected from alkyl, alkyloxy, and alkyloxycarbonyl; unsubstituted non-aromatic carbocyclyloxy; aromatic heterocyclyloxy substituted with one or more group(s) selected from alkyl, alkyloxy, and alkyloxycarbonyl; or unsubstituted aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (g-40) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is alkyl substituted with one or more group(s) selected from halogen, hydroxy, and non-aromatic heterocyclyl; unsubstituted alkyl; unsubstituted alkenyl; unsubstituted alkynyl; alkyloxy substituted with one or more group(s) selected from halogen; unsubstituted alkyloxy; alkylsulfanyl substituted with one or more group(s) selected from halogen; unsubstituted alkylsulfonyl; unsubstituted alkyloxycarbonyl: unsubstituted aromatic carbocyclyl; aromatic heterocyclyl substituted with one or more group(s) selected from alkyl and alkyloxy; unsubstituted aromatic heterocyclyl; non-aromatic heterocyclyl substituted with one or more group(s) selected from alkyl and alkyloxycarbonyl; unsubstituted non-aromatic heterocyclyl; unsubstituted non-aromatic carbocyclyloxy: or unsubstituted aromatic heterocyclyloxy,

or pharmaceutically acceptable salt thereof.

(g-41) The compound of any one of the above (g-1) to (g-34), wherein R is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (g-42) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt, thereof. (g-43) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is halogen; alkyl; haloalkyl; alkyloxy; haloaryloxy; aromatic heterocyclyl substituted with one or more group(s) selected from halogen, alkyl, haloalkyl, alkyloxy, and haloaryloxy; unsubstituted aromatic heterocyclyl; non-aromatic heterocyclyl substituted with one or more group(s) selected from halogen, alkyl, haloalkyl, alkyloxy, and haloaryloxy; unsubstituted non-aromatic heterocyclyl; aromatic heterocyclyloxy substituted with one or more group(s) selected from halogen, alkyl, haloalkyl, alkyloxy, and haloaryloxy; or unsubstituted aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (g-44) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is halogen, or pharmaceutically acceptable salt thereof. (g-45) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is a fluorine atom or a chlorine atom, or pharmaceutically acceptable salt thereof. (g-46) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (g-47) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is alkyl or haloalkyl, or pharmaceutically acceptable salt thereof. (g-48) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is substituted or unsubstituted alkyloxy, or pharmaceutically acceptable salt thereof. (g-49) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is alkyloxy or haloaryloxy, or pharmaceutically acceptable salt thereof. (g-50) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is substituted or unsubstituted aromatic heterocyclyl or substituted or unsubstituted nonaromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (g-51) The compound of any one of the above (g-1) to (g-34), wherein R 10ac is substituted or unsubstituted aromatic heterocyclyloxy or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (h) A compound according to any one of the following (h-1) to (h-34) or a pharmaceutically acceptable salt thereof. (h-1) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is a group represented by the formula:

wherein Ring F1 and Ring F2 are each independently a substituted or unsubstituted 5-membered non-aromatic carbocycle, a substituted or unsubstituted 5-membered aromatic heterocycle, or a substituted or unsubstituted 5-membered non-aromatic heterocycle;

Ring G1 and Ring G2 are each independently a substituted or unsubstituted 6-membered aromatic carbocycle, a substituted or unsubstituted 6-membered non-aromatic carbocycle, a substituted or unsubstituted 6-membered aromatic heterocycle, or a substituted or unsubstituted 6-membered non-aromatic heterocycle: Ring H1 is a substituted or unsubstituted 6-membered aromatic carbocycle, a substituted or unsubstituted 6-membered non-aromatic carbocycle, a substituted or unsubstituted 6-membered aromatic heterocycle, or a substituted or unsubstituted 6-membered non-aromatic heterocycle: p1b and p1c are each independently 0 or 1; R 9a and R 9b are the same as the above (f-1); and R 10a1 is the same as R 10a of the above (f-1),

or pharmaceutically acceptable salt thereof.

The above definition of R 3 means that R 10a1 is a substituent on Ring B.

(h-2) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(h-3) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(h-4) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(h-5) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(h-6) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(h-7) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is

or pharmaceutically acceptable salt, thereof.

(h-8) The compound of any one of the above (h-1) to (h-7), wherein Ring F1 is substituted or unsubstituted cyclopentane, substituted or unsubstituted furan, substituted or unsubstituted thiophene, substituted or unsubstituted pyrrole, substituted or unsubstituted pyrazole, substituted or unsubstituted imidazole, substituted or unsubstituted thiazole, substituted or unsubstituted oxazole, substituted or unsubstituted dihydrofuran, substituted or unsubstituted dihydrothiophene, substituted or unsubstituted dihydropyrrole, or substituted or unsubstituted dioxolo, or pharmaceutically acceptable salt thereof. (h-9) The compound of any one of the above (h-1) to (h-7), wherein Ring F1 is substituted or unsubstituted cyclopentane, substituted or unsubstituted furan, substituted or unsubstituted pyrrole, substituted or unsubstituted pyrazole, substituted or unsubstituted thiazole, substituted or unsubstituted oxazole, substituted or unsubstituted dihydrofuran, or substituted or unsubstituted dioxole, or pharmaceutically acceptable salt thereof. (h-10) The compound of any one of the above (h-1) to (h-7), wherein Ring F1 is cyclopentane substituted with one or more group(s) selected from halogen and alkyl; unsubstituted cyclopentane; furan substituted with one or more group(s) selected from halogen and alkyl; unsubstituted furan; pyrrole substituted with one or more group(s) selected from halogen and alkyl; unsubstituted pyrrole; pyrazole substituted with one or more group(s) selected from halogen and alkyl; unsubstituted pyrazole; thiazole substituted with one or more group(s) selected from halogen and alkyl; unsubstituted thiazole; oxazole substituted with one or more group(s) selected from halogen and alkyl; unsubstituted oxazole; dihydrofuran substituted with one or more group(s) selected from halogen and alkyl; unsubstituted dihydrofuran; dioxole substituted with one or more group(s) selected from halogen and alkyl; or unsubstituted dioxole,

or pharmaceutically acceptable salt thereof.

(b-11) The compound of any one of the above (h-1) to (h-7), wherein Ring F1 is unsubstituted cyclopentane; furan substituted with one or more group(s) selected from alkyl; unsubstituted pyrrole; unsubstituted pyrazole; thiazole substituted with one or more group(s) selected from alkyl; unsubstituted oxazole; unsubstituted dihydrofuran; dioxole substituted with one or more group(s) selected from halogen; or unsubstituted dioxole, or pharmaceutically acceptable salt thereof. (h-12) The compound of any one of the above (h-1) to (h-7), wherein Ring F2 is substituted or unsubstituted cyclopentane, substituted or unsubstituted furan, substituted or unsubstituted thiophene, substituted or unsubstituted pyrrole, substituted or unsubstituted pyrazole, substituted or unsubstituted imidazole, substituted or unsubstituted thiazole, substituted or unsubstituted oxazole, substituted or unsubstituted dihydrofuran, substituted or unsubstituted dihydrothiophene, or substituted or unsubstituted dihydropyrrole, or pharmaceutically acceptable salt thereof. (h-13) The compound of any one of the above (h-1) to (h-7), wherein Ring F2 is substituted or unsubstituted furan, substituted or unsubstituted pyrrole, substituted or unsubstituted thiazole, or substituted or unsubstituted dihydrofuran, or pharmaceutically acceptable salt, thereof. (h-4) The compound of any one of the above (h-1) to (h-7), wherein Ring F2 is furan substituted with one or more group(s) selected from alkyl and alkyloxy; unsubstituted furan; pyrrole substituted with one or more group(s) selected from alkyl and alkyloxy; unsubstituted pyrrole; thiazole substituted with one or more group(s) selected from alkyl and alkyloxy; unsubstituted thiazole; dihydrofuran substituted with one or more group(s) selected from alkyl and alkyloxy; or unsubstituted dihydrofuran,

or pharmaceutically acceptable salt thereof.

(h-15) The compound of any one of the above (h-1) to (h-7), wherein Ring F2 is furan substituted with one or more group(s) selected from alkyl; unsubstituted furan; unsubstituted pyrrole; thiazole substituted with one or more group(s) selected from alkyl and alkyloxy; unsubstituted thiazole; or unsubstituted dihydrofuran, or pharmaceutically acceptable salt thereof. (h-16) The compound of any one of the above (h-1) to (e-15), wherein Ring G1, and Ring G2 are each independently substituted or unsubstituted benzene, substituted or unsubstituted cyclohexane, substituted or unsubstituted pyridine, substituted or unsubstituted pyrazine, substituted or unsubstituted pyrimidine, substituted or unsubstituted pyran, substituted or unsubstituted dihydropyran, substituted or unsubstituted dihydropyridine, substituted or unsubstituted tetrahydropyridine, substituted or unsubstituted dihydropyrazine, substituted or unsubstituted tetrahydropyrazine, substituted or unsubstituted oxazine, substituted or unsubstituted dihydrooxazine, substituted or unsubstituted dioxin, or substituted or unsubstituted dihydrodioxin, or pharmaceutically acceptable salt thereof. (h-17) The compound of any one of the above (h-1) to (h-15), wherein Ring G1 and Ring G2 are each independently substituted or unsubstituted pyridine, substituted or unsubstituted pyrazine, substituted or unsubstituted pyrimidine, substituted or unsubstituted pyran, substituted or unsubstituted dihydropyran, or substituted or unsubstituted dihydrodioxin, or pharmaceutically acceptable salt thereof. (h-18) The compound of any one of the above (h-1) to (h-15), wherein Ring G1 and Ring (12 are each independently substituted or unsubstituted pyridine, substituted or unsubstituted pyran, substituted or unsubstituted dihydropyran, or substituted or unsubstituted dihydrodioxin, or pharmaceutically acceptable salt thereof. (h-19) The compound of any one of the above (h-1) to (h-15), wherein Ring G1 and Ring G2 are each independently pyridine substituted with one or more group(s) selected from halogen; unsubstituted pyridine: pyran substituted with one or more group(s) selected from halogen; unsubstituted pyran; dihydropyran substituted with one or more group(s) selected from halogen; unsubstituted dihydropyran; dihydrodioxin substituted with one or more group(s) selected from halogen; or unsubstituted dihydrodioxin,

or pharmaceutically acceptable salt thereof.

(h-20) The compound of any one of the above (h-1) to (h-15), wherein Ring G1 and Ring G2 are each independently unsubstituted pyridine; unsubstituted pyran; unsubstituted dihydropyran; dihydrodioxin substituted with one or more group(s) selected from halogen; or unsubstituted dihydrodioxin, or pharmaceutically acceptable salt thereof. (h-21) The compound of any one of the above (h-1) to (h-20), wherein Ring H1 is substituted or unsubstituted benzene, substituted or unsubstituted cyclohexane, substituted or unsubstituted pyridine, substituted or unsubstituted pyrazine, substituted or unsubstituted pyrimidine, or pharmaceutically acceptable salt thereof. (h-22) The compound of any one of the above (h-1) to (h-20), wherein Ring H1 is each independently substituted or unsubstituted benzene, or pharmaceutically acceptable salt thereof. (h-23) The compound of any one of the above (h-1) to (h-20), wherein Ring H1 is benzene substituted with one or more group(s) selected from halogen, or pharmaceutically acceptable salt thereof. (h-24) The compound of any one of the above (h-1) to (h-20), wherein Ring H1 is unsubstituted benzene, or pharmaceutically acceptable salt thereof. (h-25) The compound of any one of the above (h-1) to (h-24), wherein p1b is 0, or pharmaceutically acceptable salt thereof. (h-26) The compound of any one of the above (h-1) to (h-24), wherein p1b is 1, or pharmaceutically acceptable salt thereof. (h-27) The compound of any one of the above (h-1) to (h-26), wherein p1c is 0, or pharmaceutically acceptable salt thereof. (h-28) The compound of any one of the above (h-1) to (h-26), wherein p1c is 1, or pharmaceutically acceptable salt thereof.

(h-29) The compound of any one of the above (h-1) to (h-28), wherein R 10a1 is halogen, hydroxy, amino, carbamoyl, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, or substituted or unsubstituted alkynylamino, or pharmaceutically acceptable salt thereof.

(h-80) The compound of any one of the above (h-1) to (h-28), wherein R 10a1 is halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, or substituted or unsubstituted alkylamino, or pharmaceutically acceptable salt thereof. (h-31) The compound of any one of the above (h-1) to (h-28), wherein R 10a halogen, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy, or pharmaceutically acceptable salt thereof. (h-32) The compound of any one of the above (h-1) to (h-28), wherein R 10a1 is halogen, alkyl, haloalkyl, alkyloxy, or haloalkyloxy, or pharmaceutically acceptable salt thereof. (h-33) The compound of any one of the above (h-1) to (h-28), wherein R 10a1 is unsubstituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (h-34) The compound of any one of the above (h-1) to (h-28), wherein R 10a1 is unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (i) A compound according to any one of the following (i-1) to (i-16) or a pharmaceutically acceptable salt thereof. (i-1) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen, hydroxy, amino, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted nr unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (i-2) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen, hydroxy, amino, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (i-3) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted aromatic carbocyclyl, or substituted or unsubstituted aromatic carbocyclyloxy, or pharmaceutically acceptable salt thereof. (i-4) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen; alkyl substituted with one or more group(s) selected from halogen, alkyloxy, aromatic carbocyclyl, and aromatic heterocyclyl; unsubstituted alkyl; alkyloxy substituted with one or more group(s) selected from halogen, alkyloxy, aromatic carbocyclyl, and aromatic heterocyclyl; unsubstituted alkyloxy; alkylsulfanyl substituted with one or more group (a) selected from halogen, alkyloxy, aromatic carbocyclyl, and aromatic heterocyclyl; unsubstituted alkylsulfanyl; alkylamino substituted with one or more group(s) selected from halogen, alkyloxy, aromatic carbocyclyl, and aromatic heterocyclyl; unsubstituted alkylamino; aromatic carbocyclyl substituted with one or more group(s) selected from halogen, alkyl, and alkyloxy; unsubstituted aromatic carbocyclyl; aromatic carbocyclyloxy substituted with one or more group(s) selected from halogen, alkyl, and alkyloxy; or unsubstituted aromatic carbocyclyloxy,

or pharmaceutically acceptable salt thereof.

(i-5) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen; alkyl substituted with one or more group(s) selected from halogen, alkyloxy, aromatic carbocyclyl, and aromatic heterocyclyl; unsubstituted alkyl; alkyloxy substituted with one or more group(s) selected from halogen; unsubstituted alkyloxy; unsubstituted alkylsulfanyl; unsubstituted alkylamino; unsubstituted aromatic carbocyclyl: aromatic carbocyclyloxy substituted with one or more group(s) selected from alkyl; or unsubstituted aromatic carbocyclyloxy,

or pharmaceutically acceptable salt thereof.

(i-6) The compound of any one of Formula U) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen; alkyl substituted with one or more group(s) selected from halogen, alkyloxy, aromatic carbocyclyl, and aromatic heterocyclyl; or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (i-7) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, or substituted or unsubstituted alkynylamino, or pharmaceutically acceptable salt thereof. (i-8) The compound of any one of Formula (L) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, or substituted or unsubstituted alkylamino, or pharmaceutically acceptable salt thereof. (i-9) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen, substituted or unsubstituted alkyl, or substituted or unsubstituted alkylsulfanyl, or pharmaceutically acceptable salt thereof. (i-10) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, or substituted or unsubstituted alkynyl, or pharmaceutically acceptable salt thereof. (i-11) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen, or substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (i-12) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen, or substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (i-13) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently halogen, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (i-14) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently substituted or unsubstituted C1 to C3 alkyl, or pharmaceutically acceptable salt thereof. (i-1.5) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently unsubstituted C1 to C3 alkyl, or pharmaceutically acceptable salt thereof. (i-16) The compound of any one of Formula (I) and the above (a) to (h), wherein R 9a and R 9b are each independently unsubstituted methyl or unsubstituted ethyl, or pharmaceutically acceptable salt, thereof. (j) A compound according to any one of the following (j-1) to (j-30) or a pharmaceutically acceptable salt thereof. (j-1) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is a group represented by the Formula:

wherein Ring F3 is a substituted or unsubstituted 5-membered non-aromatic carbocycle, a substituted or unsubstituted 5-membered aromatic heterocycle, or a substituted or unsubstituted 5-membered non-aromatic heterocycle:

Ring G3 is a substituted or unsubstituted 6-membered aromatic carbocycle, a substituted or unsubstituted 6-membered non-aromatic carbocycle, a substituted or unsubstituted 6-membered aromatic heterocycle, or a substituted or unsubstituted (i-membered non-aromatic heterocycle-. Ring H2 is a substituted or unsubstituted 6-membered aromatic carbocycle, a substituted or unsubstituted 6-membered non-aromatic carbocycle, a substituted or unsubstituted 6-membered aromatic heterocycle, or a substituted or unsubstituted 6-membered non-aromatic heterocycle; p1d and p2b are each independently 0 or 1; and R 10a2 and R 10b1 are the same as R 10a and R 10b of the above (f-1),

or pharmaceutically acceptable salt thereof.

(j-2) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(j-3) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(j-4) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(j-5) The compound of any one of the above (j-1) to (j-4), wherein Ring F3 is substituted or unsubstituted cyclopentane, substituted or unsubstituted furan, substituted or unsubstituted thiophene, substituted or unsubstituted pyrrole, substituted or unsubstituted pyrazole, substituted or unsubstituted imidazole, substituted or unsubstituted thiazole, substituted or unsubstituted oxazole, substituted or unsubstituted dihydrofuran, substituted or unsubstituted dihydrothiophene, substituted or unsubstituted dihydropyrrole, or substituted or unsubstituted dioxole, or pharmaceutically acceptable salt thereof. (j-6) The compound of any one of the above (j-1) to (j-4), wherein Ring F3 is cyclopentane substituted with one or more group(s) selected from alkyl; unsubstituted cyclopentane; furan substituted with one or more group(s) selected from alkyl; unsubstituted furan; thiophene substituted with one or more group(s) selected from alkyl; unsubstituted thiophene; pyrrole substituted with one or more group(s) selected from alkyl; unsubstituted pyrrole: imidazole substituted with one or more group(s) selected from alkyl; unsubstituted imidazole; thiazole substituted with one or more group(s) selected from alkyl; unsubstituted thiazole: oxazole substituted with one or more group(s) selected from alkyl; unsubstituted oxazole; dihydrofuran substituted with one or more group(s) selected from alkyl; unsubstituted dihydrofuran; dioxole substituted with one or more group(s) selected from alkyl; or unsubstituted dioxole,

or pharmaceutically acceptable salt thereof.

(j-7) The compound of any one of the above (j-1) to (j-4), wherein Ring F3 is unsubstituted cyclopentane; unsubstituted furan: unsubstituted thiophene; pyrrole substituted with one or more group(s) selected from alkyl and an aromatic carbocycle; unsubstituted pyrrole; unsubstituted imidazole; unsubstituted thiazole; unsubstituted oxazole; unsubstituted dihydrofuran;

or unsubstituted dioxole, or pharmaceutically acceptable salt thereof.

(j-8) The compound of any one of the above (j-1) to (j-4), wherein Ring F3 is substituted or unsubstituted cyclopentane, substituted or unsubstituted furan, substituted or unsubstituted thiophene, substituted or unsubstituted pyrrole, or substituted or unsubstituted dihydrofuran, or pharmaceutically acceptable salt thereof. (j-9) The compound of any one of the above (j-1) to (j-4), wherein Ring F3 is substituted or unsubstituted furan, substituted or unsubstituted thiophene, or substituted or unsubstituted pyrrole, or pharmaceutically acceptable salt thereof. (j-10) The compound of any one of the above (j-1) to (j-4), wherein Ring F3 is furan substituted with one or more group(s) selected from alkyl; unsubstituted furan; thiophene substituted with one or more group(s) selected from alkyl; unsubstituted thiophene: pyrrole substituted with one or more group(s) selected from alkyl; or unsubstituted pyrrole, or pharmaceutically acceptable salt thereof. (j-11) The compound of any one of the above (j-1) to (j-4), wherein Ring F3 is substituted furan: unsubstituted thiophene; pyrrole substituted with one or more group(s) selected from alkyl; or unsubstituted pyrrole, or pharmaceutically acceptable salt thereof. (j-12) The compound of any one of the above (j-1) to (j-11), wherein Ring G3 is substituted or unsubstituted benzene, substituted or unsubstituted cyclohexane, substituted or unsubstituted pyridine, substituted or unsubstituted pyrazine, substituted or unsubstituted pyrimidine, substituted or unsubstituted pyran, substituted or unsubstituted dihydropyran, substituted or unsubstituted dihydropyridine, substituted or unsubstituted tetrahydropyridine, substituted or unsubstituted dihydropyrazine, substituted or unsubstituted tetrahydropyrazine, substituted or unsubstituted oxazine, substituted or unsubstituted dihydrooxazine, substituted or unsubstituted dioxin, or substituted or unsubstituted dihydrodioxin, or pharmaceutically acceptable salt thereof. (j-13) The compound of any one of the above (j-1) to (j-11), wherein Ring G3 is substituted or unsubstituted cyclohexane, substituted or unsubstituted dihydropyridine, substituted or unsubstituted tetrahydropyridine, or substituted or unsubstituted dihydrodioxin, or pharmaceutically acceptable salt thereof. (j-14) The compound of any one of the above (j-1) to (j-11), wherein Ring G3 is cyclohexane substituted with one or more group(s) selected from alkyl; unsubstituted cyclohexane; dihydropyridine substituted with one or more group(s) selected from alkyl; unsubstituted dihydropyridine; tetrahydropyridine substituted with one or more group(s) selected from alkyl; unsubstituted tetrahydropyridine: dihydrodioxin substituted with one or more group(s) selected from alkyl; or unsubstituted dihydrodioxin,

or pharmaceutically acceptable salt thereof.

(j-15) The compound of any one of the above (j-1) to (j-11), wherein Ring (<3 is unsubstituted cyclohexane; dihydropyridine substituted with one or more group(s) selected from alkyl; unsubstituted dihydropyridine; unsubstituted tetrahydropyridine, or unsubstituted dihydrodioxin, or pharmaceutically acceptable salt thereof. (j-16) The compound of any one of the above (j-1) to (j-11), wherein Ring G3 is unsubstituted cyclohexane; dihydropyridine substituted with one or more group(s) selected from alkyl; or unsubstituted dihydropyridine, or pharmaceutically acceptable salt thereof. (j-17) The compound of any one of the above (j-1) to (j-16), wherein Ring H2 is substituted or unsubstituted benzene, substituted or unsubstituted cyclohexane, substituted or unsubstituted pyridine, substituted or unsubstituted pyrazine, substituted or unsubstituted pyrimidine, or pharmaceutically acceptable salt, thereof. (j-18) The compound of any one of the above (j-1) to (j-16), wherein Ring H2 is each independently substituted or unsubstituted benzene, or pharmaceutically acceptable salt thereof. (j-19) The compound of any one of the above (j-1) to (j-16), wherein Ring H2 is benzene substituted with one or more group(s) selected from halogen, or pharmaceutically acceptable salt, thereof. (j-20) The compound of any one of the above (j-1) to (j-16), wherein Ring H2 is unsubstituted benzene, or pharmaceutically acceptable salt thereof. (j-21) The compound of any one of the above (j-1) to (j-20), wherein p1d is 0, or pharmaceutically acceptable salt thereof. (j-22) The compound of any one of the above (j-1) to (j-20), wherein p1d is 1, or pharmaceutically acceptable salt thereof. (j-23) The compound of any one of the above (j-1) to (j-22), wherein p2b is 0, or pharmaceutically acceptable salt thereof. (j-24) The compound of any one of the above (j-1) to (j-22), wherein p2b is 1, or pharmaceutically acceptable salt thereof. (j-25) The compound of any one of the above (j-1) to (j-21), wherein R 10a2 and R 10b1 are each independently halogen, hydroxy, amino, carbamoyl, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfanyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, or substituted or unsubstituted alkynylamino, or pharmaceutically acceptable salt thereof. (j-26) The compound of any one of the above (j-1) to (j-24), wherein R 10a2 and R 10b1 are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, or substituted or unsubstituted alkylamino, or pharmaceutically acceptable salt thereof. (j-27) The compound of any one of the above (j-1) to (j-24), wherein R 10a1 and R 10b1 are each independently halogen, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy, or pharmaceutically acceptable salt thereof. (j-28) The compound of any one of the above (j-1) to (j-24), wherein R 10a2 and R 10b1 are each independently halogen, alkyl, haloalkyl, alkyloxy, or haloaryloxy, or pharmaceutically acceptable salt thereof. (j-29) The compound of any one of the above (j-1) to (j-24), wherein R 10a2 and R 10b1 are each independently halogen or unsubstituted or unsubstituted alkyl, or

pharmaceutically acceptable salt thereof.

(j-30) The compound of any one of the above (j-1) to (j-24), wherein R 10a2 and R 10b1 are each independently halogen or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (k) A compound according to any one of the following (k-1) to (k-11) or a pharmaceutically acceptable salt thereof. (k 1) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is

or pharmaceutically acceptable salt thereof.

The above definition of R 3 means that R 10c is a substituent, on Ring B, and R 10e is a substituent on Ring D.

(k-2) The compound of any one of Formula (I) and the above (a) to (e), wherein R 3 is

or pharmaceutically acceptable salt thereof.

(k-3) The compound of the above (k-1) or (k-2), wherein R 10c and R 10d are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (k-4) The compound of the above (k-1) or (k-2), wherein R 10c and R 10d are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, or substituted or unsubstituted non-aromatic heterocyclyloxy, or pharmaceutically acceptable salt thereof. (k-5) The compound of the above (k-1) or (k-2), wherein R 10c and R 10d are each independently halogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, or pharmaceutically acceptable salt thereof. (k-6) The compound of the above (k-1) or (k-2), wherein R 10c and R 10d are each independently halogen, alkyl, haloalkyl, alkyloxy, haloalkyloxy, or pharmaceutically acceptable salt thereof. (k-7) The compound of the above (k-1) or (k-2), wherein R 10c and R 10d are each independently halogen, or pharmaceutically acceptable salt thereof. (k-8) The compound of any one of the above (k-1) to (k-7), wherein R 10e is each independently halogen, or substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (k-9) The compound of any one of the above (k-1) to (k-7), wherein R 10e is each independently halogen, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (k-10) The compound of any one of the above (k-1) to (k-7), wherein R 10e is each independently halogen, or pharmaceutically acceptable salt thereof. (k-11) The compound of any one of the above (k-1) to (k-10), wherein p3 is 0, or pharmaceutically acceptable salt thereof. (l) A compound according to any one of the following (l-1) to (l-6) or a pharmaceutically acceptable salt thereof. (l-1) The compound of any one of Formula (I) and the above (a) to (k), wherein Ring B is benzene, cyclohexene, or a 6-membered aromatic heterocycle, or pharmaceutically acceptable salt thereof. (l-2) The compound of any one of Formula (I) and the above (a) to (k), wherein Ring B is benzene, or a 6-membered aromatic heterocycle, or pharmaceutically acceptable salt thereof. (l-3) The compound of any one of Formula (I) and the above (a) to (k), wherein Ring B is benzene, cyclohexene, pyridine, pyrimidine, or pyrazine, or pharmaceutically acceptable salt, thereof. (l-4) The compound of any one of Formula (I) and the above (a) to (k), wherein Ring B is benzene, pyridine, pyrimidine, or pyrazine, or pharmaceutically acceptable salt thereof. (l-5) The compound of any one of Formula (I) and the above (a) to (k), wherein Ring B is benzene, or pyridine, or pharmaceutically acceptable salt thereof. (l-6) The compound of any one of Formula (I) and the above (a) to (k), wherein Ring B is benzene, or pharmaceutically acceptable salt thereof. (m) A compound according to any one of the following (m-1) to (m-4) or a pharmaceutically acceptable salt thereof. (m-1) The compound of any one of Formula (I) and the above (a) to (l), wherein Ring C is cyclopentane, or a 5-membered aromatic heterocycle, or pharmaceutically acceptable; salt thereof. (m-2) The compound of any one of Formula (I) and the above (a) to (l), wherein Ring C is a 5-membered aromatic heterocycle, or pharmaceutically acceptable salt thereof. (m-3) The compound of any one of Formula (I) and the above (a) to (l), wherein Ring C is cyclopentane, pyrrole, imidazole, pyrazole, furan, thiophene, isoxazole, oxazole, isothiazole, or thiazole, or pharmaceutically acceptable salt thereof. (m-4) The compound of any one of Formula (I) and the above (a) to (l), wherein Ring C is thiophene, or pharmaceutically acceptable salt thereof. (n) A compound according to any one of the following (n-1) to (n-19) or a pharmaceutically acceptable salt thereof. (n-1) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkylsulfamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkylsulfonylamino, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non-aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylsulfanyl, substituted or unsubstituted non-aromatic carbocyclylsulfanyl, substituted or unsubstituted aromatic heterocyclylsulfanyl, substituted or unsubstituted non-aromatic heterocyclylsulfanyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsxdistituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylsulfonyl, substituted or unsubstituted non-aromatic carbocyclylsulfonyl, substituted or unsubstituted aromatic heterocyclylsulfonyl, substituted or unsubstituted non-aromatic heterocyclylsulfonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylsulfamoyl, substituted or unsubstituted non-aromatic carbocyclylsulfamoyl, substituted or unsubstituted aromatic heterocyclylsulfamoyl, substituted or unsubstituted non-aromatic heterocyclylsulfamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonylamino, substituted or unsubstituted aromatic heterocyclylcarbonylamino, substituted or unsubstituted non-aromatic heterocyclylcarbonyl amino, substituted or unsubstituted aromatic carbocyclylsulfonylamino, substituted or unsubstituted non-aromatic carbocyclylsulfonylamino, substituted or unsubstituted aromatic heterocyclylsulfonylamino, or substituted or unsubstituted non-aromatic heterocyclylsulfonylamino, or pharmaceutically acceptable salt thereof. (n-2) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a hydrogen atom, halogen, hydroxy, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylamino, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclyloxy, substituted or unsubstituted non aromatic carbocyclyloxy, substituted or unsubstituted aromatic heterocyclyloxy, substituted or unsubstituted non-aromatic heterocyclyloxy, substituted or unsubstituted aromatic carbocyclylamino, substituted or unsubstituted non-aromatic carbocyclylamino, substituted or unsubstituted aromatic heterocyclylamino, substituted or unsubstituted non-aromatic heterocyclylamino, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, substituted or unsubstituted aromatic carbocyclylcarbonylamino, substituted or unsubstituted non-aromatic carbocyclylcarbonylamino, substituted or unsubstituted aromatic heterocyclylcarbonylamino, or substituted or unsubstituted non-aromatic heterocyclylcarbonylamino, or pharmaceutically acceptable salt thereof. (n-8) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyl oxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alky ylcarbamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted alkenyloxycarbonylamino, substituted or unsubstituted alkynyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (n-4) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylamino, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (n-5) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (n-6) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkyloxycarbonylamino, or substituted or unsubstituted aromatic carbocyclyl, or pharmaceutically acceptable salt, thereof. (n-7) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a hydrogen atom; halogen; hydroxy; carboxy; amino; carbamoyl; cyano; alkyl substituted with one or more group(s) selected from halogen, hydroxy, carboxy, carbamoyl, alkylcarbamoyl optionally substituted with one or more group(s) selected from (hydroxy, cyano and alkyloxy), non-aromatic heterocyclylcarbonyl, aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from (halogen and alkyl), and non-aromatic heterocyclyl carbamoyl; unsubstituted alkyl; alkyloxy substituted with one or more group(s) selected from halogen and an aromatic carbocycle; unsubstituted alkyloxy; unsubstituted alkyloxycarbonyl; alkylcarbamoyl substituted with one or more group(s) selected from halogen, cyano, alkyloxy, alkylcarbonyl, alkylsulfonyl, alkylcarbamoyl, and aromatic carbocyclyl; unsubstituted alkylcarbamoyl; unsubstituted alkyloxycarbonylamino; or unsubstituted aromatic carbocyclyl,

or pharmaceutically acceptable salt thereof.

(N-8) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5A is a hydrogen atom; halogen; alkyl substituted with one or more group(s) selected from halogen, hydroxy, carboxy, carbamoyl, alkylcarbamoyl optionally substituted with one or more group(s) selected from (hydroxy, cyano and alkyloxy), non-aromatic heterocyclylcarbonyl, aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from (halogen and alkyl), and non-aromatic heterocyclyl carbamoyl; unsubstituted alkyl; alkyloxy substituted with one or more group(s) selected from halogen and an aromatic carbocycle; or unsubstituted alkyloxy,

or pharmaceutically acceptable salt, thereof.

(n-9) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a hydrogen atom, halogen, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (n-10) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a hydrogen atom, halogen, amino, carbamoyl, cyano, alkyl, haloalkyl, alkyloxy, haloaryloxy, alkylamino, haloalkylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (n-11) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a hydrogen atom, halogen, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy, or pharmaceutically acceptable salt thereof. (n-12) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a hydrogen atom, halogen, alkyl, haloalkyl, alkyloxy, or haloalkyloxy, or pharmaceutically acceptable salt thereof. (n-13) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is substituted or unsubstituted alkyloxy, or pharmaceutically acceptable salt thereof. (n-14) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is alkyloxy or haloalkyloxy, or pharmaceutically acceptable salt thereof. (n-15) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (n-10) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is alkyl or haloalkyl, or pharmaceutically acceptable salt thereof. (n-17) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is halogen, or pharmaceutically acceptable salt thereof. (n-18) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a fluorine atom or a chlorine atom, or pharmaceutically acceptable salt thereof. (n-19) The compound of any one of Formula (I) and the above (a) to (m), wherein R 5a is a fluorine atom, or pharmaceutically acceptable salt thereof. (o) A compound according to any one of the following (o-1) to (o-9) or a pharmaceutically acceptable salt thereof. (o-1) The compound of any one of Formula (I) and the above (a) to (n), wherein R 5b is a hydrogen atom, carboxy, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, or substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, or pharmaceutically acceptable salt thereof. (o-2) The compound of any one of Formula (I) and the above (a) to (n), wherein R 5b is a hydrogen atom, carboxy, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl, substituted or unsubstituted aromatic carbocyclylcarbonyl, substituted or unsubstituted non-aromatic carbocyclylcarbonyl, substituted or unsubstituted aromatic heterocyclylcarbonyl, substituted or unsubstituted non-aromatic heterocyclylcarbonyl, substituted or unsubstituted aromatic carbocyclylcarbamoyl, substituted or unsubstituted non-aromatic carbocyclylcarbamoyl, substituted or unsubstituted aromatic heterocyclylcarbamoyl, or substituted or unsubstituted non-aromatic heterocyclylcarbamoyl, or pharmaceutically acceptable salt thereof. (o-3) The compound of any one of Formula (I) and the above (a) to (n), wherein R 5b is a hydrogen atom, carboxy, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted alkenylcarbonyl, substituted or unsubstituted alkynylcarbonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (o-4) The compound of any one of Formula (L) and the above (a) to (n), wherein R 5b is a hydrogen atom, substituted or unsubstituted alkyl, substituted or unsubstituted alkylcarbonyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (o-5) The compound of any one of Formula (I) and the above (a) to (n), wherein R 5b is a hydrogen atom, or substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (o-6) The compound of any one of Formula (I) and the above (a) to (n), wherein R 5b is a hydrogen atom, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (o-7) The compound of any one of Formula (I) and the above (a) to (n), wherein R 5b is unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (o-8) The compound of any one of Formula (L) and the above (a) to (n), wherein R 5b is a hydrogen atom; carboxyl carbamoyl; cyano; alkyl substituted with one or more group(s) selected from halogen, hydroxy, carboxy, carbamoyl, alkylcarbamoyl optionally substituted with one or more group(s) selected from (hydroxy, cyano and alkyloxy), non-aromatic heterocyclylcarbonyl, aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from (halogen and alkyl), and non-aromatic heterocyclylcarbamoyl; unsubstituted alkyl; unsubstituted alkyloxycarbonyl; alkylcarbamoyl substituted with one or more group(s) selected from halogen, cyano, alkyloxy, alkylcarbonyl, alkylsulfonyl, alkylcarbamoyl, and aromatic carbocyclyl; unsubstituted alkylcarbamoyl; or unsubstituted aromatic carbocyclyl,

or pharmaceutically acceptable salt thereof.

(o-9) The compound of any one of Formula ft) and the above (a) to (n), wherein R 5b is a hydrogen atom; halogen; alkyl substituted with one or more group (a) selected from halogen, hydroxy, carboxy, carbamoyl, alkylcarbamoyl optionally substituted with one or more group(s) selected from (hydroxy, cyano and alkyloxy), non-aromatic heterocyclylcarbonyl, aromatic carbocyclylcarbamoyl optionally substituted with one or more group(s) selected from (halogen and alkyl), and non-aromatic heterocyclylcarbamoyl;

or unsubstituted alkyl, or pharmaceutically acceptable salt thereof.

(p) A compound of any one of the following (p-1) to (p-3) or a pharmaceutically acceptable salt thereof. (p-1) The compound of any one of Formula (I) and the above (a) to (o), wherein n is an integer from 1 to 3, or pharmaceutically acceptable salt thereof. (p-2) The compound of any one of Formula (I) and the above (a) to (o), wherein n is 1 or 2, or pharmaceutically acceptable salt thereof. (p-3) The compound of any one of Formula (I) and the above (a) to (o), wherein n is 1, or pharmaceutically acceptable salt thereof. (q) A compound according to any one of the following (q-1) to (q-7) or a pharmaceutically acceptable salt thereof. (q-1) The compound of any one of Formula (I) and the above (a) to (p), wherein R 2a is a hydrogen atom, halogen, or substituted or unsubstituted alkyl, or R 2a and R 2b which are attached to the same carbon atom are taken together to form oxo, or pharmaceutically acceptable salt thereof. (q-2) The compound of any one of Formula (I) and the above (a) to (p), wherein R 2a is a hydrogen atom, or halogen, or R 2a and R 2b which are attached to the same carbon atom are taken together to form oxo, or pharmaceutically acceptable salt thereof. (q-3) The compound of any one of Formula (I) and the above (a) to (p), wherein R 2a is a hydrogen atom, or R 2a and R 2b which are attached to the same carbon atom are taken together to form oxo, or pharmaceutically acceptable salt thereof. (q-4) The compound of any one of Formula (I) and the above (a) to (p), wherein R 2a is a hydrogen atom, halogen, or substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (q-5) The compound of any one of Formula (I) and the above (a) to (p), wherein R 2a is a hydrogen atom, halogen, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (q-6) The compound of any one of Formula (I) and the above (a) to (p), wherein R 2a is a hydrogen atom, or halogen, or pharmaceutically acceptable salt thereof. (q-7) The compound of any one of Formula (I) and the above (a) to (p), wherein R 2a is a hydrogen atom, or pharmaceutically acceptable salt thereof. (r) A compound according to any one of the following (r-1) to (r-7) or a pharmaceutically acceptable salt thereof. (r-1) The compound of any one of Formula (I) and the above (a) to (q), wherein R 2b is a hydrogen atom, halogen, or substituted or unsubstituted alkyl, or R 2a and R 2b which are attached to the same carbon atom are taken together to form oxo, or pharmaceutically acceptable salt thereof. (r-2) The compound of any one of Formula (I) and the above (a) to (q), wherein R 2b is a hydrogen atom, or halogen, or R 2a and R 2b which are attached to the same carbon atom are taken together to form oxo, or pharmaceutically acceptable salt thereof. (r-3) The compound of any one of Formula (I) and the above (a) to (q), wherein R 2b is a hydrogen atom, or R 2a and R 2b which are attached to the same carbon atom are taken together to form oxo, or pharmaceutically acceptable salt thereof. (r-4) The compound of any one of Formula (I) and the above (a) to (q), wherein R 2b is a hydrogen atom, halogen, or substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (r-5) The compound of any one of Formula (I) and the above (a) to (q), wherein R 2b is a hydrogen atom, halogen, alkyl, or haloalkyl, or pharmaceutically acceptable salt, thereof. (r-6) The compound of any one of Formula (I) and the above (a) to (q), wherein R 2b is a hydrogen atom, or halogen, or pharmaceutically acceptable salt thereof. (r-7) The compound of any one of Formula (I) and the above (a) to (q), wherein R 2b is a hydrogen atom, or pharmaceutically acceptable salt thereof. (s) A compound according to any one of the following (s-1) to (s-3) or a pharmaceutically acceptable salt thereof. (s-1) The compound of any one of Formula (I) and the above (a) to (r), wherein m is an integer from 0 to 2, or pharmaceutically acceptable salt thereof. (s-2) The compound of any one of Formula (I) and the above (a) to (r), wherein m is 0 or 1, or pharmaceutically acceptable salt thereof. (a-3) The compound of any one of Formula (I) and the above (a) to (r), wherein m is 0, or pharmaceutically acceptable salt thereof. (t) A compound according to any one of the following (t-1) to (t-4) or a pharmaceutically acceptable salt, thereof. (t-1) The compound of any one of Formula (I) and the above (a) to (s), wherein R 2c is a hydrogen atom, halogen, or substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (t-2) The compound of any one of Formula (I) and the above (a) to (s), wherein R 2c is a hydrogen atom, halogen, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (t-3) The compound of any one of Formula (I) and the above (a) to (s), wherein R 2c is a hydrogen atom, or halogen, or pharmaceutically acceptable salt thereof. (t-4) The compound of any one of Formula (I) and the above (a) to (s), wherein R 2c is a hydrogen atom, or pharmaceutically acceptable salt thereof. (u) A compound according to any one of the following (u-1) to (u-4) or a pharmaceutically acceptable salt thereof. (u-1) The compound of any one of Formula (I) and the above (a) to (t), wherein R 2d is a hydrogen atom, halogen, or substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (u-2) The compound of any one of Formula (I) and the above (a) to (t), wherein R 2d is a hydrogen atom, halogen, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (u-3) The compound of any one of Formula (I) and the above (a) to (t), wherein R 2d is a hydrogen atom, or halogen, or pharmaceutically acceptable salt thereof. (u-4) The compound of any one of Formula (I) and the above (a) to (t), wherein R 2d is a hydrogen atom, or pharmaceutically acceptable salt thereof. (v) A compound according to any one of the following (v-1) to (v-4) or a pharmaceutically acceptable salt thereof. (v-1) The compound of any one of Formula (I) and the above (a) to (u), wherein Y 1 is O, or pharmaceutically acceptable salt thereof. (v-2) The compound of any one of Formula (I) and the above (a) to (u), wherein Y 2 is O, or pharmaceutically acceptable salt thereof. (v-3) The compound of any one of Formula (I) and the above (a) to (u), wherein each of Y 1 and Y 2 is O, or pharmaceutically acceptable salt thereof. (v-4) The compound of any one of Formula (I) and the above (a) to (u), wherein Y 1 and Y 2 are each independently O or S, or pharmaceutically acceptable salt, thereof. (w) A compound according to any one of the following (w-1) to (w-4) or a pharmaceutically acceptable salt thereof. (w-1) The compound of any one of Formula (I) and the above (a) to (v), wherein R 4 is a hydrogen atom, halogen, or substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (w-2) The compound of any one of Formula (I) and the above (a) to (v), wherein R 4 is a hydrogen atom, halogen, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (w-3) The compound of any one of Formula (I) and the above (a) to (v), wherein R 4 is a hydrogen atom, or halogen, or pharmaceutically acceptable salt thereof. (w-4) The compound of any one of Formula (I) and the above (a) to (v), wherein R 4 is a hydrogen atom, or pharmaceutically acceptable salt thereof. (x) A compound according to any one of the following (x-1) to (x-4) or a pharmaceutically acceptable salt thereof. (x-1) The compound of any one of Formula (I) and the above (a) to (w), wherein R 6 is a hydrogen atom, halogen, or substituted or unsubstituted alkyl, or pharmaceutically acceptable salt thereof. (x-2) The compound of any one of Formula (I) and the above (a) to (w), wherein R 6 is a hydrogen atom, halogen, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (x-3) The compound of any one of Formula (I) and the above (a) to (w), wherein R 6 is a hydrogen atom, or halogen, or pharmaceutically acceptable salt thereof. (x-4) The compound of any one of Formula (I) and the above (a) to (w), wherein R 6 is a hydrogen atom, or pharmaceutically acceptable salt thereof. (y) A compound according to any one of the following (y-1) to (y-8) or a pharmaceutically acceptable salt thereof. (y-1) The compound of any one of Formula (I) and the above (a) to (x), wherein R 5a′ is a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, sulfamoyl, sulfo, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted alkylamino, substituted or unsubstituted alkenylamino, substituted or unsubstituted alkynylamino, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkenylsulfonyl, substituted or unsubstituted alkynylsulfanyl, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkenyloxycarbonyl, substituted or unsubstituted alkynyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkenylcarbamoyl, substituted or unsubstituted alkynylcarbamoyl, substituted or unsubstituted alkylcarbonylamino, substituted or unsubstituted alkenylcarbonylamino, substituted or unsubstituted alkynylcarbonylamino, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted alkenyloxycarbonylamino, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (y-2) The compound of any one of Formula (I) and the above (a) to (x), wherein R 5a′ is a hydrogen atom, halogen, hydroxy, carboxy, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkyloxycarbonyl, substituted or unsubstituted alkylcarbamoyl, substituted or unsubstituted alkyloxycarbonylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (y-3) The compound of any one of Formula (I) and the above (a) to (x), wherein R 5a′ is a hydrogen atom, halogen, amino, carbamoyl, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkylamino, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (y-4) The compound of any one of Formula (I) and the above (a) to (x), wherein R 5a′ is a hydrogen atom, halogen, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy, or pharmaceutically acceptable salt thereof. (y-5) The compound of any one of Formula (I) and the above (a) to (x), wherein R 5a′ is a hydrogen atom, halogen, alkyl, haloalkyl, alkyloxy, or haloaryloxy, or pharmaceutically acceptable salt thereof. (y-6) The compound of any one of Formula (I) and the above (a) to (x), wherein R 5a′ is a hydrogen atom, halogen, alkyl, or haloalkyl, or pharmaceutically acceptable salt thereof. (y-7) The compound of any one of Formula (I) and the above (a) to (x), wherein R 5a′ is a hydrogen atom, or halogen, or pharmaceutically acceptable salt thereof. (y-8) The compound of any one of Formula (I) and the above (a) to (x), wherein R 5a′ is a hydrogen atom, or pharmaceutically acceptable salt thereof. (z) A compound according to any one of the following (z-1) to (z-4) or a pharmaceutically acceptable salt thereof. (z-1) The compound of any one of Formula (I) and the above (a) to (y), wherein R Y is each independently a hydrogen atom, hydroxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, substituted or unsubstituted alkynyloxy, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, or substituted or unsubstituted non-aromatic heterocyclyl, or pharmaceutically acceptable salt thereof. (z-2) The compound of any one of Formula (I) and the above (a) to (y), wherein R Y is each independently a hydrogen atom, hydroxy, cyano, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted alkenyloxy, or substituted or unsubstituted alkynyloxy, or pharmaceutically acceptable salt thereof. (z-3) The compound of any one of Formula (I) and the above (a) to (y), wherein R Y is each independently a hydrogen atom, hydroxy, cyano, substituted or unsubstituted alkyl, or substituted or unsubstituted alkyloxy, or pharmaceutically acceptable salt thereof. (z-4) The compound of any one of Formula (I) and the above (a) to (y), wherein R Y is each independently a hydrogen atom, hydroxy, cyano, alkyl, haloalkyl, alkyloxy, or haloaryloxy, or pharmaceutically acceptable salt thereof.

The compounds represented by Formula (I) are not limited to specific isomers but include all possible isomers (e.g., keto-enol isomers, imine-enamine isomers, diastereoisomers, enantiomers, rotamers or the like), racemates or mixtures thereof.

For example, a compound represented by Formula (I) wherein R 7a is a hydrogen atom includes the following tautomer.

Likewise, a tautomer of the ring represented by the Formula:

is included.

In the present specification, in a group represented by the Formula:

p1 hydrogen atom(s) which is attached to a ring-constituting atom on Ring B can be replaced with R 10a and R 10c .

In the present specification, in a group represented by the Formula:

p2 hydrogen atom(s) which is attached to a ring-constituting atom on Ring C can be replaced with R 10b and R 10d .

In the present, specification, in a group represented by the Formula:

p3 hydrogen atom(s) which is attached to a ring-constituting atom on Ring 1) can be replaced with R 10e .

In the present specification, in a group represented by the formula:

p1a hydrogen atom(s) which is attached to a ring-constituting atom on Ring B can be replaced with R 11a . Also, any hydrogen atom which is attached to a ring-constituting atom on Ring B can be replaced with R 11c .

In the present specification, in a group represented by the Formula:

p2a hydrogen atom(s) which is attached to a ring-constituting atom on Ring C can be replaced with R 11b . Also, any hydrogen atom which is attached to a ring-constituting atom on Ring C can be replaced with R 11a .

In the present specification, in a group represented by the Formula:

q1 hydrogen atom(s) which is attached to a ring-constituting atom on Ring E can be replaced with R 12 . q2 hydrogen atom(s) which is attached to a ring-constituting atom on Ring E can be replaced with R 13 . q3 hydrogen atom(s) which is attached to a ring-constituting atom on Ring F can be replaced with R 14 .

In the present specification, in a group represented by the Formula:

p1b hydrogen atom(s) which is attached to a ring-constituting atom on Ring B can be replaced with R 10a1 .

In the present, specification, in a group represented by the Formula:

p1c hydrogen atom(s) which is attached to a ring constituting atom on Ring B can be replaced with R 10a1 .

In the present specification, in a group represented by the Formula:

p1d hydrogen atom(s) which is attached to a ring-constituting atom on Ring B can be replaced with R 10a2 . p2b hydrogen atom(s) which is attached to a ring-constituting atom on Ring C can be replaced with R 10b1 .

One or more hydrogen, carbon and/or other atoms in the compounds represented by Formula (I) may be replaced with isotopes of hydrogen, carbon and/or other atoms respectively. Example s of isotopes include hydrogen, carbon, nitrogen, oxygen, phosphorus, sulfur, fluorine, iodine and chlorine, such as 2 H, 3 H, 11 C, 13 C, 14 C, 15 N, 18 O, 17 O, 31 P, 32 P, 35 S, 18 F, 123 I and 36 Cl respectively. The compounds represented by Formula (I) include the compounds replaced with these isotopes. The compounds replaced with the above isotopes are useful as medicines and include all of radiolabeled compounds of the compound of Formula (I). A “method of radiolabeling” in the manufacture of the “radiolabeled compounds” is encompassed by the present, invention, and the “radiolabeled compounds” are useful for studies on metabolized drug pharmacokinetics, studies on binding assay and/or diagnostic tools.

A radiolabeled compound of the compounds represented by Formula (I) can be prepared using well-known methods in the art. For example, a tritium-labeled compound represented by Formula (I) can be prepared by introducing a tritium to a certain compound represented by Formula (I), through a catalytic dehalogenation reaction using a tritium. This method comprises reacting with an appropriately-halogenated precursor of the compound represented by Formula (I) with tritium gas in the presence of an appropriate catalyst, such as Pd/C, and in the presence or absent of a base. The other appropriate method of preparing a tritium-labeled compound can be referred to “Isotopes in the Physical and Biomedical Sciences, Vol. 1, Labeled Compounds (Part A), Chapter 6 (1987)”. A 14 C-labeled compound can be prepared by using a raw material having 14 C.

The pharmaceutically acceptable salts of the compounds represented by Formula (D include, for example, salts with alkaline metal (e.g., lithium, sodium, potassium or the like), alkaline earth metal (e.g., calcium, barium or the like), magnesium, transition metal (e.g., zinc, iron or the like), ammonia, organic bases (e.g., trimethylamine, triethylamine, dicyclohexylamine, ethanolamine, diethanolamine, triethanolamine, meglumine, ethylenediamine, pyridine, picoline, quinoline or the like) or amino acids, or salts with inorganic acids (e.g., hydrochloric acid, sulfuric acid, nitric acid, carbonic acid, hydrobromic acid, phosphoric, acid, hydroiodic acid or the like) or organic acids (e.g., formic acid, acetic acid, propionic acid, trifluoroacetic acid, citric acid, lactic acid, tartaric acid, oxalic acid, maleic acid, fumaric acid, mandelic acid, glutaric acid, malic acid, benzoic acid, phthalic acid, ascorbic acid, benzenesulfonic acid, p-toluenesulfonic acid, methanesulfonic acid, ethanesulfonic acid or the like). Especially, salts with hydrochloric acid, sulfuric acid, phosphoric acid, tartaric acid, methanesulfonic acid and the like are included. These salts can be formed by the usual methods.

The compounds represented by Formula (I) of the present invention or pharmaceutically acceptable salts thereof may form solvates (e.g., hydrates or the like) and/or crystal polymorphs. The present invention encompasses those various solvates and crystal polymorphs. “Solvates” may be those wherein any numbers of solvent molecules (e.g., water molecules or the like) are coordinated with the compounds represented by Formula (I). When the compounds represented by Formula (I) or pharmaceutically acceptable salts thereof are allowed to stand in the atmosphere, the compounds may absorb water, resulting in attachment of adsorbed water or formation of hydrates. Recrystallization of the compounds represented by Formula (I) or pharmaceutically acceptable salts thereof may produce crystal polymorphs.

The compounds represented by Formula (I) of the present, invention or pharmaceutically acceptable salts thereof may form prodrugs. The present invention also encompasses such various prodrugs. Prodrugs are derivatives of the compounds of the present invention that have chemically or metabolically degradable groups, and compounds that are converted to the pharmaceutically active compounds of the present invention through solvolysis or under physiological conditions in vivo. Prodrugs include compounds that are converted to the compounds represented by Formula (I) through enzymatic oxidation, reduction, hydrolysis or the like under physiological conditions in vivo, compounds that are converted to the compounds represented by Formula (I) through hydrolysis by gastric acid etc., and the like. Methods for selecting and preparing suitable prodrug derivatives are described in, for example, “Design of Prodrugs, Elsevier. Amsrdam, 1985”. Prodrugs themselves may have some activity.

When the compounds represented by Formula (I) or pharmaceutically acceptable salts thereof have hydroxyl group(s), prodrugs include acyloxy derivatives and sulfonyloxy derivatives that are prepared by, for example, reacting compounds having hydroxyl group(s) with suitable acyl halide, suitable acid anhydride, suitable sulfonyl chlorido, suitable sulfonyl anhydride and mixed anhydride, or with a condensing agent. For example, they include CH 3 COO—, C 2 H 5 COO—, tert-BuCOO—, C 15 H 31 COO—, PhCOO—, (m-NaOOCPh)COO—, NaOOCCH 2 CH 2 COO—, CH 3 CH(NH 2 )COO—, CH 2 N(CH 3 ) 2 COO—, CH 3 SO 3 —, CH 3 CH 2 SO 3 —, CF 3 SO 3 —, CH 2 FSO 3 —, CF 3 CH 2 SO 3 —, p-CH 3 O-PhSO 3 —, PhSO 3 — and p-CH 3 PhSO 3 —.

The compounds of the present invention have an antagonistic activity for the P2X7 receptor, and therefore, are useful as a therapeutic and/or preventive agent for diseases associated with the P2X7 receptor. As the diseases associated with the P2X7 receptor, pain, central nervous system diseases, immune diseases and inflammatory diseases and the like, preferably pain are exemplified (Non-patent Document 7-8 and Patent Document 1 etc.).

As pain, pain associated with zoster, postherpetic neuralgia, trigeminal neuralgia, thalamic pain, cancer pain, postoperative pain, menstrual pain, labor pain, chest pain, abdominal pain, colic pain, lumbar backache, headache, migraine, sciatica, sore muscle, orofacial pain, toothache, glossagra, shoulder pain, nociceptive pain, pain associated with deafferentation, psychogenic pain and the like; pain associated with the disease such as entrapment neuropathy, carpal canal syndrome, diabetes, Guillain-Barre syndrome, myofascial pain syndrome, fibromyalgia syndrome, complex regional pain syndrome, causalgia, Hansen's disease, spinal cord injury, stroke, multiple sclerosis, Parkinson's disease, endometriosis, hernia of intervertebral disk, arthritis, rheumatoid arthritis, osteoarthritis, cervical spondylosis deformans, spinal canal stenosis, thoracic outlet syndrome, traumatic brachial plexus injury syndrome, shoulder-hand syndrome, whiplash injury, cholelithiasis, pancreatitis, cystitis, urethritis, urinary calculosis, prostatitis, ulcerative colitis, Crohn's disease, irritable bowel syndrome, bone fracture, osteoporosis, gout, cauda equina syndrome, ankylosing spondylitis, painful spasm, ABC syndrome, skin disease, arteriosclerosis obliterans, Buerger's disease, Raynaud's phenomenon, gangrene, temporomandibular arthrosis, somatoform disorder, somatization disorder, depression and the like;

pain associated with drug therapy, and pain associated with radiation therapy are exemplified.

Additionally, effects for opioid tolerance can be expected.

As central nervous system diseases, Alzheimer's disease, Cerebral amyloid angiopathy, Parkinson's disease, Creutzfeldt-Jakob disease, Huntington's chorea, depression, schizophrenia, attention deficit hyperactivity disorder, sleep disorder, autism spectrum disorder, epilepsy, stroke, multiple sclerosis, spinal cord injury, amyotrophic lateral sclerosis, opioid dependence, cocaine dependence, nicotine dependence and the like are exemplified.

Preferably, as central nervous system diseases, Alzheimer's disease, Cerebral amyloid angiopathy, Parkinson's disease, depression, schizophrenia, attention deficit hyperactivity disorder, sleep disorder, autism spectrum disorder, epilepsy, stroke, multiple sclerosis, spinal cord injury, amyotrophic lateral sclerosis, opioid dependence, cocaine dependence, nicotine dependence and the like are exemplified.

As immune diseases and inflammatory diseases, rheumatoid arthritis, osteoarthritis, asthma, bronchitis, chronic obstructive pulmonary disease, pulmonary emphysema, septic shock, hepatitis, hepatic fibrosis, hepatic cirrhosis, cholecystitis, glomerulonephritis, nephrotic syndrome, pancreatitis, cystitis, urethritis, prostatitis, ulcerative colitis, Crohn's disease, irritable bowel syndrome, psoriasis, atopic dermatitis, contact dermatitis, eczematous dermatitis, delayed-type hypersensitivity reaction, conjunctivitis, uveitis, growth and metastasis of malignant cell (prostate cancer, breast, cancer, lung cancer, uterine cancer, pancreatic cancer, colorectal cancer etc.), leukemia, meningitis, burn injury, glossitis, gingivitis, periodontal disease, esophagitis and the like are exemplified. It is possible that rejection associated with allograft or blood transfusion is involved in the P2X7 receptor. As the other diseases associated with the P2X7 receptor, circulatory diseases such as atherosclerosis, ischemic heart disease, diabetes and the like, bone diseases such as osteoporosis, bone Paget's disease, osteonecrosis, temporomandibular arthrosis and the like, and urologic diseases such as overactive bladder, stress urinary incontinence, prostatomegaly and the like are exemplified.

Preferably, as immune diseases and inflammatory diseases, rheumatoid arthritis, arthritis, osteoarthritis, asthma, bronchitis, chronic obstructive pulmonary disease, cystitis, ulcerative colitis, Crohn's disease and the like are exemplified.

(Synthetic Procedures for the Compound of the Present Invention)

For example, the compounds represented by Formula (I) of the present invention can be prepared by the general procedures described below. The starting materials and reaction reagents used in such synthesis are commercially available or can be synthesized according to methods well known in the art using the compounds commercially available. The methods for extraction, purification and the like may be carried out by using the usual method for the experiments of organic chemistry.

The compounds of the present invention can be synthesized by referring to the known methods in the art.

In all the following steps, when a substituent which interferes with the reaction, e.g. hydroxy, mercapto, amino, formyl, carbonyl, carboxy, is possessed, the substituent is protected by the method such as those described in Protective Groups in Organic Synthesis, Theodora W Greene (John Wiley & Sons) in advance, and the protective group may be removed at a desirable step.

During all the following steps, the order of the steps to be performed may be appropriately changed. In each step, an intermediate may be isolated and then used in the next step.

In this description, meanings of each abbreviation are as follows:

DIEA: N,N-diisopropylethylamine DMF: N,N-dimethylformamide DMSO: Dimethyl sulfoxide DPPA: Diphenylphosphoryl azide IPE: Diisopropyl ether NBS: N-bromosuccinimide NMP: N-methylpyrrolidone HATU: O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate HOAt: 1-hydroxy-7-azabenzotriazole PdCl 2 (dppf): [1,1′-bis(diphenylphosphino)ferrocene]palladium (II) dichloride Xantphos: 4,5′-bis(diphenylphosphino)-9,9′-dimethylxanthene

[Method A]

wherein G 1 , G 2 and G 3 are each independently a leaving group such as halogen, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylsulfinyl, or substituted or unsubstituted alkylsulfonyl; and the other symbols are the same as the above (1).

A compound (A-2) can be synthesized by the reaction of a compound (A-1) with a basic aqueous solution.

As the base, for example, metal hydroxide (e.g., sodium hydroxide, potassium hydroxide, lithium hydroxide etc.), metal carbonate (e.g., sodium carbonate, potassium carbonate, cesium carbonate etc.) and the like are exemplified. 1.0 or more mole equivalent(s), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (A-1).

As the reaction solvent, ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), DMF, DMSO, NMP, water and a mixed solvent thereof and the like are exemplified.

The reaction temperature is 0° C. to 40° C., preferably 0° C. to 20° C.

The reaction time is 0.5 to 48 hours, preferably 1 to 16 hours.

The obtained desired compound (A-2) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (A-4) can be synthesized by the reaction of the compound (A-2) with a compound (A-3) in the presence of a base in the appropriate solvent.

In this reaction, 1.0 or more mole equivalent(s) of the compound (A-3), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (A-2).

As the base, for example, metal hydroxide (e.g., sodium hydroxide, potassium hydroxide, tripotassium phosphate etc.), metal hydride (e.g., sodium hydride, lithium hydride etc.), metal carbonate (e.g., sodium carbonate, potassium carbonate, cesium carbonate etc.), metal alkoxide (e.g., sodium methoxide, sodium ethoxide, potassium tert-butoxide etc.), metal alkyl (e.g., butyllithium etc.), pyridine, triethylamine. DIEA and the like are exemplified. 1.0 or more mole equivalent(s), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent, of the compound (A-2).

As the reaction solvent, aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), halogenated hydrocarbons (e.g., chloroform, dichloromethane etc.), DMF, DMSO, NMP, acetonitrile, pyridine, water and the like are exemplified. The reaction solvent may be used alone or in combination.

The reaction temperature is 0 to 200° C., under microwave irradiation as necessary, preferably 0 to 150° C.

The reaction time is 0.1 to 72 hours, preferably 0.0 hours to 18 hours.

The obtained desired compound (A-4) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (1α) can be synthesized by the reaction of the compound (A-4) with a compound (A-5) in the presence of a palladium catalyst and a base or an acid without any solvent or in the appropriate solvent as necessary.

In this reaction, 1.0 or more mole equivalent(s) of the compound (A-5), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (A-4).

As the base, for example, metal hydroxide (e.g., sodium hydroxide, potassium hydroxide, tripotassium phosphate etc.), metal hydride (e.g., sodium hydride, lithium hydride etc.), metal carbonate (e.g., sodium carbonate, potassium carbonate, cesium carbonate etc.), metal alkoxide (e.g., sodium methoxide, sodium ethoxide, potassium tert-butoxide etc.), metal alkyl (e.g., butyllithium etc.), pyridine, triethylamine, DIEA and the like are exemplified. 1.0 or more mole equivalent(s), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (A-4).

As the acid, for example, acetic acid, propionic acid and the like are exemplified. 1.0 or more mole equivalent(s), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (A-4).

As the palladium catalyst, palladium acetate, bis(dibenzylideneacetone)palladium, tetrakistriphenylphosphinepalladium, bis(triphenylphosphine)palladium(II) dichloride, bis(tri-tert-butylphosphine)palladium, PdCl 2 (dppf) CH 2 Cl 2 and the like are exemplified. 0.001 to 0.5 mole equivalents can be used per an equivalent of the compound (A-4).

As the reaction solvent, alcohols (e.g., tert-butanol, isopropanol etc.), aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), halogenated hydrocarbons (e.g., chloroform, dichloromethane etc.), DMF, DMSO, NMP, acetonitrile, pyridine, water and the like are exemplified. The reaction solvent may be used alone or in combination.

The reaction temperature is 0 to 200° C., under microwave irradiation as necessary, preferably 0 to 150° C.

The reaction time is 0.1 to 72 hours, preferably 0.5 hours to 18 hours.

The obtained desired compound (1α) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method B]

wherein G 1 and G 3 are the same as the method A, and the other symbols are the same as the above (1).

A compound (B-2) can be synthesized by the reaction of a compound (B-1) with the compound (A-3) according to the synthetic procedures described in the step 2 of the method A.

The obtained desired compound (B-2) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (16) can be synthesized by the reaction of the compound (B-2) with the compound (A-5) according to the synthetic procedures described in the step 3 of the method A.

The obtained desired compound (IB) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method C]

wherein G 1 and G 3 are the same as the method A, and the other symbols are the same as the above (1).

A compound (C-2) can be synthesized by the reaction of a compound (C-1) with the compound (A-3) according to the synthetic procedures described in the step 2 of the method A.

The obtained desired compound (C-2) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (Iy) can be synthesized by the reaction of the compound (C-2) with the compound (A-5) according to the synthetic procedures described in the step 3 of the method A.

The obtained desired compound (Iy) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method D]

wherein PG 1 is an appropriate protecting group of a hydroxy group;

G 1 and G 3 are the same as the method A, and the other symbols are the same as the above (1).

A compound (D-2) can be synthesized by the reaction of a compound (A-1) with a compound (D-1) in the presence of a base in the appropriate solvent.

In this reaction. 1.0 or more mole equivalents) of the compound (D-1), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (A-1).

As the base which can be used, for example, metal hydride (e.g., sodium hydrido, lithium hydrido etc.), molal carbonato (e.g., sodium carbonato, potassium bicarbonate, cesium carbonate etc.), metal alkoxide (e.g., sodium methoxide, sodium ethoxide, potassium tert-butoxide etc.), metal alkyl (e.g., butyllithium etc.) are exemplified. 1.0 or more mole equivalents), preferably 1.0 to 1.5 mole equivalents) can be used per an equivalent of the compound (A-1).

As the reaction solvent, alcohols (e.g., tert-butanol, isopropanol etc.), aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), DMF, DMSO, NMP, a mixed solvent thereof and the like are exemplified.

As the reaction temperature, −20° C. to 200° C., preferably 0° C. to 30° C. are exemplified.

As the reaction time, 0.1 to 80 hours, preferably 1 to 16 hours are exemplified.

The obtained desired compound (D-2) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (D-3) can be synthesized by the reaction of the compound (D-2) with the compound (A-5) according to the synthetic procedures described in the step 3 of the method A.

The obtained desired compound (D-3) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (D-4) can be synthesized by the deprotection of the compound (D-3) in the presence of an acid or a Lewis acid or a base in the appropriate solvent.

As the acid, hydrochloric acid-ethyl acetate, hydrochloric acid-methanol, hydrochloric acid-dioxane, hydrobromic acid-acetic acid, hydrobromic acid, sulfuric acid, formic acid, trifluoroacetic acid and the like are exemplified. As the Lewis acid, trimethylsilyl iodide, BBr 3 , AlCl 3 , BF 3 .(Et 2 O) and the like are exemplified. As the base, tetrabutyl ammonium fluoride, hydrogen fluoride-pyridine and the like are exemplified. 0.01 or more mole equivalents, preferably 0.5 to 10.0 mole equivalents can be used per an equivalent of the compound (D-3).

As the reaction solvent, alcohols (e.g., methanol, ethanol, isopropanol etc.), aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), halogenated hydrocarbons (e.g., chloroform, dichloromethane etc.), DMF, DMSO, NMP, acetonitrile, DMA, pyridine, water and the like are exemplified. The reaction solvent may be used alone or in combination.

The reaction temperature is 0 to 200° C., under microwave irradiation as necessary, preferably 0 to 150° C.

The reaction time is 0.1 to 72 hours, preferably 0.5 hours to 18 hours.

The obtained desired compound (D-4) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (1α) can be synthesized by the reaction of the compound (D-4) with the compound (A-3) according to the synthetic procedures described in the step 2 of the method B.

The obtained desired compound (1α) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method E]

wherein R A and R B are each independently hydrogen, or substituted or unsubstituted alkyl, or are taken together to form a substituted or unsubstituted non-aromatic heterocycle)

Hal is halogen; PG 1 is an appropriate protecting group of a hydroxy group) G 1 and G 3 are the same as the method A, and the other symbols are the same as the above (1).

A compound (E-3) can be synthesized by the reaction of the compound (E-1) with boronic acid or boronate ester (E-2) in the presence of a metal catalyst and a base in the appropriate solvent.

In this reaction, 1.0 or more mole equivalent(s) of boronic acid or boronate ester (E-2), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (E-1).

As the metal catalyst, palladium (II) acetate, bis(dibenzylideneacetone)palladium, Tetrakistriphenylphosphinepalladium, bis(triphenylphosphine)palladium (II) dichloride, bis(tri-tert-butylphosphine)palladium, PdCl 2 (dppF)CH 2 Cl 2 and the like are exemplified. 0.001 to 1.0 mole equivalents) can be used per an equivalent of the compound (E-1).

As the base, lithium hydroxide, sodium hydroxide, potassium hydroxide, potassium tert-butoxide, sodium tert-butoxide, sodium carbonate, cesium carbonate, potassium bicarbonate, sodium hydrogen carbonate, sodium phosphate, sodium hydrogen phosphate, potassium phosphate, potassium hydrogen phosphate and the like can be exemplified. 1.0 to 10.0 mole equivalent(s) can be used per an equivalent of the compound (E-1).

As the reaction solvent, aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.). DMF, DMA, NMP, DMSO, water and a mixed solvent thereof and the like are exemplified.

The reaction temperature is 20 to 250° C., under microwave irradiation as necessary, preferably 0 to 200° C.

The reaction time is 0.1 to 48 hours, preferably 0.5 to 12 hours.

The obtained desired compound (E-3) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (E-4) can be synthesized by the reaction of the compound (E-3) with the compound (A-5) according to the synthetic procedures described in the step 2 of the method D.

The obtained desired compound (E-4) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (E-5) can be synthesized by the deprotection of the protecting group of the hydroxy group of the compound (E-4) according to the synthetic procedures described in the step 3 of the method D.

The obtained desired compound (E-5) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (Iα-1) can be synthesized by the reaction of the compound (E-5) with the compound (A-3) according to the synthetic procedures described in the step 2 of the method B.

The obtained desired compound (Iα-1) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method F]

wherein each symbol is the same as the above (1).

A compound (F-2) can be synthesized by the reaction of the compound (F-1) with 2,2,2,6-tetramethylpiperidino 1-oxyl in the presence of an oxidizing agent.

As the oxidizing agent, for example, sodium hypochlorite, iodobenzene diacetate and the like are exemplified. 1.0 or more mole equivalents), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (F-1).

As the reaction solvent, ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), halogenated hydrocarbons (e.g., chloroform, dichloromethane etc.), acetonitrile, water and the like are exemplified. The reaction solvent may be used alone or in combination.

The reaction temperature is 0 to 100° C., preferably 0 to 60° C.

The reaction time is 0.1 to 72 hours, preferably 0.5 hours to 18 hours.

The obtained desired compound (F-2) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (F-1) can be synthesized by the reaction of the compound (F-2) with a compound (F-3) in the presence of a base in the appropriate solvent.

In this reaction, 1.0 or more mole equivalent(s) of the compound (F-3), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (F-2).

As the base, for example, metal hydroxide (e.g., sodium hydroxide, potassium hydroxide, tripotassium phosphate etc.), metal hydride (e.g., sodium hydride, lithium hydride etc.), metal carbonato (e.g., sodium carbonato, potassium carbonate, cesium carbonate etc.), metal alkoxide (e.g., sodium methoxide, sodium ethoxide, potassium tert-butoxide etc.), metal alkyl (e.g., butyllithium etc.), pyridine, triethylamine, DIEA and the like are exemplified. 1.0 or more mole equivalent(s), preferably 1.0 to 5.0 mole equivalent(s) can be need per an equivalent of the compound (F-2).

As the reaction solvent, alcohols (e.g., tertbutanol, isopropanol etc.), aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), halogenated hydrocarbons (e.g., chloroform, dichloromethane etc.), DMF, DMSO, NMP, acetonitrile, pyridine, water and the like are exemplified. The reaction solvent may be used alone or in combination.

The reaction temperature is 0 to 200° C., under microwave irradiation as necessary, preferably 0 to 1.50° C.

The reaction time is 0.1 to 72 hours, preferably 0.5 to 18 hours.

The obtained desired compound (F-4) can lie purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (F-5) can be synthesized by the reaction of the compound (F-4) with iodine in a DMSO solution.

The reaction temperature is −10° C. to 200° C., preferably 0° C. to 150° C.

The reaction time is 0.1 to 72 hours, preferably 0.5 hours to 18 hours.

The obtained desired compound (F-5) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (Iα-2) can be synthesized by the reaction of the compound (F-5) with the compound (A-5) according to the synthetic procedures described in the step 3 of the method A.

The obtained desired compound (Iα-2) can be purified os necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method G]

wherein R D and R E are each independently substituted or unsubstituted alkyl; G 3 is the same as the method A, and the other symbols are the same as the above (1).

A compound (G-1) can be synthesized by the reaction of the compound (A-5) with 1-amidinopyrazole hydrochloride.

In this reaction, 1.0 or more mole equivalent(s) of the 1-amidinopyrazole hydrochloride, preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (A-5).

As the base, for example, metal hydroxide (e.g., sodium hydroxide, potassium hydroxide, tripotassium phosphate etc.), metal hydride (e.g., sodium hydride, lithium hydride etc.), metal carbonate (e.g., sodium carbonate, potassium bicarbonate, cesium carbonate etc.), metal alkoxide (e.g., sodium methoxide, sodium ethoxide, potassium tertbutoxide etc.), metal alkyl (e.g., butyllithium etc.), pyridine, triethylamine, DIEA and the like are exemplified. 1.0 or more mole equivalent(s), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (A-5).

As the reaction solvent, aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), halogenated hydrocarbons (e.g., chloroform, dichloromethane etc.), DMF, DMSO, NMP, acetonitrile, DMA and the like are exemplified. The reaction solvent may be used alone or in combination.

The reaction temperature is 0 to 200° C., under microwave irradiation as necessary, preferably 0 to 150° C.

The reaction time is 0.1 to 72 hours, preferably 0.5 to 18 hours.

The obtained desired compound (G-1) can be purified as necessary by the methods which ore usually used (e.g., column chromatography, recrystallization etc.).

A compound (G-3) can be synthesized by the reaction of the compound (G-1) with a compound (G-2) in the presence of a base in the appropriate solvent.

In this reaction, 1.0 or more mole equivalent(s) of the compound (G-2), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (G-1).

As the base, for example, metal hydroxide (e.g., sodium hydroxide, potassium hydroxide, tripotassium phosphate etc.), metal hydride (e.g., sodium hydride, lithium hydride etc.), metal carbonate (e.g., sodium carbonate, potassium carbonate, cesium carbonate etc.), metal alkoxide (e.g., sodium methoxide, sodium ethoxide, potassium tertbutoxide etc.), metal alkyl (e.g., butyllithium etc.), triethylamine, DIEA, DBU and the like are exemplified. 1.0 or more mole equivalent(s), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (G-1).

As the reaction solvent, alcohols (e.g., tertbutanol, isopropanol etc.), aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), DMF, NMP, acetonitrile. DMA and the like are exemplified. The reaction solvent can be used alone or in combination.

The reaction temperature is 0 to 200° C., under microwave irradiation as necessary, preferably 0 to 150° C.

The reaction time is 0.1 to 72 hours, preferably 0.5 hours to 18 hours.

The obtained desired compound (G-3) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (Iγ-1) can be synthesized by the reaction of the compound (G-3) and a compound (A-3) according to the synthetic procedures described in the step 2 of the method A.

The obtained desired compound (Iγ-1) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

The synthesis methods of methods H to N shown below can be used not only in the synthesis of a compound represented by formula (Iα) but also in the synthesis of compounds represented by formula (Iβ) and formula (Iγ).

[Method H]

wherein PC 2 is an appropriate protecting group of a hydroxy group;

G 1 and G 4 are each independently a leaving group such as halogen, substituted or unsubstituted alkylsulfanyl, substituted or unsubstituted alkylsulfinyl, or substituted or unsubstituted alkylsulfonyl; R 5aa is a hydrogen atom, a hydrogen atom, a substituent selected from the substituent group B, or the like; and the other symbols are the same as the above (1).

A compound (H-2) can be synthesized by the deprotection of the protecting grovip of the hydroxy group of the compound (H-1) obtained by the method A according to the synthetic procedures described in the step 3 of the method D.

The obtained desired compound (H-2) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (H-4) can be synthesized by the reaction of the compound (H-2) and a compound (H-3) according to the synthetic procedures described in the step 2 of the method A.

The obtained desired compound (H-4) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound represented by a compound (Iα-3) can be synthesized by the reaction of the compound (H-4) and a compound (A-5) according to the synthetic procedures described in the step 3 of the method A.

The obtained desired compound (Iα-3) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method I]

wherein R 5ab is substituted or unsubstituted alkyl; and

the other symbols are the same as the above (1>.

A compound (Iα-5) can be synthesized by reduction using the compound (Iα-4) obtained by the method A in the appropriate solvent.

As the reducing agent, sodium borohydride, lithium borohydride, lithium aluminum hydride and the like are exemplified. 1 or more mole equivalent(s), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (Iα-4).

As the reaction solvent, alcohols (e.g., methanol, ethanol, isopropanol etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), dichloromethane, water and the like are exemplified. The reaction solvent may be used alone or in combination.

The reaction temperature is −10 to 100° C., preferably 0 to 100° C.

The reaction time is 0.1 to 72 hours, preferably 0.5 hours to 18 hours.

The obtained desired compound (Iα-5) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method J]

wherein R 5ab is substituted or unsubstituted alkyl;

R 5ac and R 5ad are each independently a hydrogen atom, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aromatic carbocyclyl, substituted or unsubstituted non-aromatic carbocyclyl, substituted or unsubstituted aromatic heterocyclyl, substituted or unsubstituted non-aromatic heterocyclyl or the like; and

the other symbols ore the same as the above (1).

A compound (Iα-6) can be synthesized by hydrolysis using the compound (Iα-4) obtained by the method A in the presence of an acid or a base.

As the acid, hydrochloric acid, p-toluenesulfonic acid, sulfuric acid, formic acid, trifluoroacetic acid and the like are exemplified.

As the base, lithium hydroxide, sodium hydroxide, potassium hydroxide, sodium carbonate, cesium carbonate, potassium carbonate, sodium hydrogen carbonate, sodium phosphate, sodium hydrogen phosphate, potassium phosphate, potassium hydrogen phosphato, tetrabutyl ammonium fluoride and the like are exemplified.

1 or more mole equivalent(s), preferably 5 mole equivalents can be used per an equivalent of the compound (Iα-4).

As the reaction solvent, alcohols (e.g., methanol, ethanol, isopropanol etc.), aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), DMF, DMSO, NMP, acetonitrile. DMA, water and the like are exemplified. The reaction solvent may be used alone or in combination.

The reaction temperature is −10 to 200° C., preferably 0 to 150° C.

The reaction time is 0.1 to 72 hours, preferably 0.5 hours to 18 hours.

The obtained desired compound (Iα-7) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (Iα-7) can be synthesized by the condensation of the compound (Iα-6) with the compound (J-1) in the appropriate solvent.

As the condensing agent, condensing agents such as 1-hydroxybenzotriazole, HOAt, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, HATU, and (benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate, and bases such as triethylamine and diisopropylethylamine, and the like are exemplified. 1 or more mole equivalent(s), preferably 1 to 5 mole equivalent(s) can be used per an equivalent of the compound (Iα-6).

As the reaction solvent, aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), DMF, NMP, acetonitrile, DMA and the like are exemplified. The reaction solvent can be used alone or in combination.

The reaction temperature is −10 to 200° C., preferably 0 to 150° C.

The reaction time is 0.1 to 72 hours, preferably 0.0 hours to 18 hours.

The obtained desired compound (Iα-7) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method K]

wherein Hal is halogen;

R A and R B are the same as the method E, and the other symbols are the same as the above (1).

A compound (Iα-9) can be synthesized by the reaction of the compound (Iα-8) obtained by the method A with a boronic acid or a boronic acid ester (E-2) according to the synthetic procedures described in the method E.

The obtained desired compound (Iα-9) can bo purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method L]

wherein R 5ac is substituted or unsubstituted alkyl, and the other symbols are the same as the above (1).

A compound (Iα-11) can be synthesized by the hydrolysis of the compound (Iα-10) obtained by the method A according to the synthetic procedures described in the step 1 of the method J.

The obtained desired compound (Iα-11) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method M]

wherein R 5ac and R 5ad are the same as the method J, and the other symbols are the same as the above (1).

A compound (Iα-12) can be synthesized by the condensation of the compound (Iα-10) obtained by the method K with the compound (J-1) according to the synthetic procedures described in the step 2 of the method J.

The obtained desired compound (Iα-12) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method N]

wherein R 5af is substituted or unsubstituted alkyl, substituted or unsubstituted aromatic carbocyclyl, or substituted or unsubstituted aromatic heterocyclyl, and the other symbols are the same as the above (1).

A compound (Iα-13) can be synthesized by the reaction of the compound (Iα-11) obtained by the method K with an alcohol (N-1) in the presence of DPPA in the appropriate solvent.

As the reaction solvent, aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), DMF, DMSO, NMP, acetonitrile, DMA and the like are exemplified. The reaction solvent can be used alone or in combination.

The reaction temperature is −10 to 200° C., preferably 0 to 150° C.

The reaction time is 0.1 to 72 hours, preferably 0.5 hours to 18 hours.

The obtained desired compound (Iα-13) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

In the synthesis of the compound of the present invention, C═O can be appropriately converted to C═S at a desirable step on the basis of the synthesis method of method O shown below. [Method O]

wherein each symbol is the same as the above (1).

A compound (Iα′) can be synthesized by the reaction of the compound (Iα) obtained by the method A with 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphethane-2,4-disulfide in the appropriate solvent.

As the reaction solvent, aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), acetonitrile and the like are exemplified. The reaction solvent can be used alone or in combination.

The reaction temperature is −10 to 110° C., preferably 0 to 80° C.

The reaction time is 0.1 to 72 hours, preferably 0.5 hours to 18 hours.

The obtained desired compound (Iα′) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method P]

wherein R 5ag is substituted or unsubstituted alkyl, substituted or unsubstituted aromatic carbocyclyl, or substituted or unsubstituted aromatic heterocyclyl, G 1 and G 3 are the same as the method A, and the other symbols are the same as the above (1).

A compound (P-2) can be synthesized by the reaction of a compound (P-1) with an acid chloride in the presence of a base in the appropriate solvent.

As the acid chloride, for example, phosphoryl chloride, thionyl chloride, oxalyl chloride and the like are exemplified. 1.0 or more mole equivalent(s), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (P-1).

As the base, for example, pyridine, triethylamine, DIEA and the like are exemplified.

As the reaction solvent, aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), halogenated hydrocarbons (e.g., chloroform, dichloromethane etc.) ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), and a mixed solvent thereof and the like are exemplified.

The reaction temperature is 0° C. to 100° C., preferably 0° C. to 20° C.

The reaction time is 0.5 hours to 48 hours, preferably 1 hour to 12 hours.

The obtained desired compound (P-2) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (P-4) can be synthesized by the reaction of the compound (P-2) with a compound (P-3) in the appropriate solvent.

In this reaction, 1.0 or more mole equivalent(s) of the compound (P-3), preferably 1.0 to 3.0 mole equivalent(s) can be used per an equivalent of the compound (P-2).

As the reaction solvent, alcohols (e.g., methanol, ethanol, tert-butanol, isopropanol etc.), aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), DMF, NMP, acetonitrile, DMA and the like are exemplified. The reaction solvent, can be used alone or in combination.

The reaction temperature is 0 to 100° C., preferably 0 to 40° C.

The reaction time is 0.5 to 48 hours, preferably 1 hour to 8 hours.

The obtained desired compound (P-4) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (P-5) can be synthesized by the reaction of the compound (P-4) with a basic aqueous solution according to the synthetic procedures described in the step 1 of the method A.

The obtained desired compound (P-5) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (P-6) can be synthesized by the reaction of the compound (P-5) with the compound (A-3) according to the synthetic procedures described in the step 2 of the method A.

The obtained desired compound (P-6) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (Iα-14) can be synthesized by the reaction of the compound (P-6) with the compound (A-5) according to the synthetic procedures described in the step 3 of the method A.

The obtained desired compound (Iα-14) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

[Method Q]

wherein R F is substituted or unsubstituted alkyl; and the other symbols are the same as the above (1).

A compound (Q-3) can be synthesized by the reaction of a compound (Q-1) with a compound (Q-2) in the presence of an acid in the appropriate solvent.

In this reaction, 1.0 or more mole equivalent(s) of the compound (Q-2), preferably 1.0 to 2.0 mole equivalent(s) can be used per an equivalent of the compound (Q-1).

As the acid, for example, acetic acid, trifluoroacetic acid, p-toluenesulfonic acid and the like are exemplified. 0.05 or more mole equivalents, preferably 0.1 to 2.0 mole equivalents can be used per an equivalent of the compound (Q-1).

As the reaction solvent, alcohols (e.g., methanol, ethanol, tert-butanol, isopropanol etc.), aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), DMF, NMP, acetonitrile, DMA and the like are exemplified. The reaction solvent can be used alone or in combination.

The reaction temperature is 0° C. to 100° C., preferably 0° C. to 20° C.

The reaction time is 0.5 hours to 48 hours, preferably 1 hour to 12 hours.

The obtained desired compound (Q-3) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (Q-4) can be synthesized by the reaction of the compound (Q-3) with trimethylsilyl isothiocyanate in the appropriate solvent or without, any solvent.

As the reaction solvent, alcohols (e.g., methanol, ethanol, tort-butanol, isopropanol etc.), aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), DMF, NMP, acetonitrile, DMA and the like are exemplified. The reaction solvent can be used alone or in combination.

The reaction temperature is 0° C. to 200° C., preferably 40° C. to 150° C.

The reaction time is 0.5 hours to 48 hours, preferably 1 hour to 12 hours.

The obtained desired compound (Q-4) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (Q-5) can be synthesized by the reaction of the compound (Q-4) with methyl iodide in the presence of a base in the appropriate solvent.

As the base, for example, metal hydroxide (e.g., sodium hydroxide, potassium hydroxide, tripotassium phosphate etc.), metal hydride (e.g., sodium hydride, lithium hydride etc.), metal carbonate (e.g., sodium carbonate, potassium carbonate, cesium carbonate etc.), metal alkoxide (e.g., sodium methoxide, sodium ethoxide, potassium tert-butoxide etc.), metal alkyl (e.g., butyllithium etc.), pyridine, triethylamine, DIEA and the like are exemplified. 1.0 or more mole equivalent(s), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (Q-4).

As the reaction solvent, aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), DMF, NMP, acetonitrile. DMA and the like are exemplified. The reaction solvent can be used alone or in combination.

The reaction temperature is 0° C. to 100° C., preferably 0° C. to 40° C.

The reaction time is 0.5 hours to 48 hours, preferably 1 hour to 8 hours.

The obtained desired compound (Q-5) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

A compound (Iα-15) can be synthesized by the reaction of the compound (Q-5) with the compound (A-5) according to the synthetic procedures described in the step 3 of the method A.

The obtained desired compound (Iα-15) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

In the synthesis of the compound of the present invention, C═S can be appropriately converted to C═N(R Y ) at a desirable step on the basis of the synthesis method of method ft shown below.

[Method R]

wherein Y 1s is C═N(R Y ), and the other symbols are the same as the above (1).

A compound (Iα″) can be synthesized by the reaction of the compound (Iα′) obtained by the method Q with a compound (R-1) in the presence of an acid or a base in the appropriate solvent.

In this reaction, 1.0 or more mole equivalent(s) of the compound (R-1), preferably 1.0 to 5.0 mole equivalent(s) can be used per an equivalent of the compound (Iα′).

As the acid, for example, acetic acid, trifluoroacetic acid, p-toluenesulfonic acid and the like are exemplified. 0.05 or more mole equivalents, preferably 0.1 to 2.0 mole equivalents can be used per an equivalent of the compound (1α′).

As the base, for example, pyridine, triethylamine, DIEA and the like are exemplified. 1.0 or more mole equivalent(s), preferably 1.0 to 20.0 mole equivalent(s) can be used per an equivalent of the compound (Iα′).

As the reaction solvent, alcohols (e.g., methanol, ethanol, tert-butanol, isopropanol etc.), aromatic hydrocarbons (e.g., toluene, benzene, xylene etc.), saturated hydrocarbons (e.g., cyclohexane, hexane etc.), ethers (e.g., tetrahydrofuran, diethyl ether, dioxane, dimethoxyethane etc.), DMF, NMP, acetonitrile, DMA and the like are exemplified. The reaction solvent can be used alone or in combination.

The reaction temperature is 0 to 150° C., preferably 0 to 80° C.

The reaction time is 0.1 to 72 hours, preferably 0.5 hours to 18 hours.

The obtained desired compound (Iα″) can be purified as necessary by the methods which are usually used (e.g., column chromatography, recrystallization etc.).

An optically active form of the compound represented by Formula (I) can be produced by using an optically active starting material, synthesizing an optically active intermediate by asymmetric synthesis at an appropriate step, or optically resolving racemic intermediates or final products at an appropriate step. The approach for the optical resolution includes a method of resolving optical isomers using an optically active column, kinetic optical resolution using enzymatic reaction or the like, crystallization and resolution of diastereomers by salt formation using a chiral acid or a chiral base, preferential crystallization and the like.

The preferred compound of the present invention not only has an antagonistic activity for the P2X7 receptor but also is useful as a medicine and has any or all of the following superior characteristics:

a) The inhibitory activity for CYP enzymes (e.g., CYP1A2, CYP2C9, CYP2C19, CYP2D6, CYP3A4 and the like) is weak. b) The compound demonstrates good pharmacokinetics, such as a high bioavailability, moderate clearance and the like. c) The compound has a high metabolic stability. d) The compound has no irreversible inhibitory effect against CYP enzymes (e.g., CYP3A4) when the concentration is within the range described in the present description as the measurement conditions. e) The compound has no mutagenicity. f) The compound is associated with a low cardiovascular risk. g) The compound has a high solubility. h) The compound has a high selectivity for the P2X7 receptor (e.g., high selectivity in the other receptors of the P2X family). i) The compound has a high brain distribution.

A pharmaceutical composition of the present invention can be administered orally or parenterally. Methods for parenteral administration include dermal, subcutaneous, intravenous, intraarterial, intramuscular, intraperitoneal, transmucosal, inhalation, transnasal, ophthalmic, inner ear or vaginal administration and the like.

In case of oral administration, any forms, which are usually used, such as oral solid formulations (e.g., tablets, powders, granules, capsules, pills, films or the like), oral liquid formulations (e.g., suspension, emulsion, elixir, syrup, lemonade, spirit, aromatic water, extract, decoction, tincture or the like) and the like may prepared according to the usual method and administered. The tablets can be sugar-coated tablets, film-coated tablets, enteric-coating tablets, sustained-release tablets, troche tablets, sublingual tablets, buccal tablets, chewable tablets or orally dispersing tablets. Powders and granules can be dry syrups. Capsules can be soft capsules, micro capsules or sustained-release capsules.

In case of parenteral administration, any forms, which are usually used, such as injections, drips, external preparations (e.g., ophthalmic drops, nasal drops, ear drops, aerosols, inhalations, lotion, infusion, liniment, mouthwash, enema, ointment, plaster, jelly, cream, patch, cataplasm, external powder, suppository or the like) and the like can be preferably administered. Injections can be emulsions whose type is O/W, W/O, O/W/O, W/O/W or the like.

The pharmaceutical composition may be manufactured by mixing an effective amount of the compound of the present invention with various pharmaceutical additives suitable for the formulation, such as excipients, binders, moistening agents, disintegrants, lubricants, diluents and the like. Furthermore, the pharmaceutical composition can be for pediatric patients, geriatric patients, serious cases or operations by appropriately changing the effective amount of the compound of the present invention, formulation and/or various pharmaceutical additives. The pediatric pharmaceutical compositions are preferably administered to patients under 12 or 15 years old. In addition, the pediatric pharmaceutical compositions can be administered to patients who are under 27 days old after the birth, 28 days to 23 months old after the birth, 2 to 11 years old, 12 to 16 years old, or 18 years old. The geriatric pharmaceutical compositions are preferably administered to patients who are 65 years old or over.

Although the dosage of a pharmaceutical composition of the present invention should be determined in consideration of the patient's age and body weight, the type and degree of diseases, the administration route and the like, a usual oral dosage is 0.05 to 100 and preferably 0.1 to 10 mg/kg/day. For parenteral administration, although the dosage highly varies with administration routes, a usual dosage is 0.005 to 10 and preferably 0.01 to 1 mg/kg/day. The dosage may be administered in one to several divisions per day.

The present, invention will be described in more detail with reference to, hut not limited to, the following Examples, Reference Examples and Test Examples.

NMR analysis of each example was performed by 400 MHz using DMSO-d 6 , or CDCl 3 .

“RT” in tables means retention time in LC/MS: liquid column chromatography/mass analysis and these are measured under the conditions as below:

Condition [1]

Column: Shim-pack XR-ODS (2.2 μm, i.d. 50×3.0 mm) (Shimadzu)

Flow rate: 1.6 mL/min

UV detection wavelength: 254 nm

Mobile phases: [A] is 0.1% formic acid solution, and [B] is 0.1% formic acid in acetonitrile solvent.

Gradient: linear gradient of 10% to 100% solvent [B] for 3 minutes was performed, and 100% solvent [B] was maintained for 0.5 minute.

Condition [2]

Column: ACQUITY HPLC (registered trademark BEH C18 (1.7 μm

i.d.2.1×50 mm)(Waters)

Flow rate: 0.8 mL/min

UV detection wavelength: 254 nm

Mobile phases: [A] is 10 mmol/L Ammonium Carbonate solution, and [B] is acetonitrile.

Gradient: linear gradient of 5% to 100% solvent [B] for 3.5 minutes was performed, and 100% solvent [B] was maintained for 0.5 minute.

Condition [3]

Column: ACQUITY UPLC (registered trademark) BEH C18 (1.7 μm

i.d. 2.1×50 mm)(Waters)

Flow rate: 0.8 mL/min

UV detection wavelength: 254 nm

Mobile phases: [A] is 0.1% formic acid solution, and [B] is 0.1% formic acid in acetonitrile solvent.

Gradient: linear gradient of 5% to 100% solvent [B] for 3.5 minutes was performed, and 100% solvent [B] was maintained for 0.5 minute.

In the structural formulas of the compounds described in Examples, the following bonding pattern means a double bond and represents that stereoscopic information on E-Z conformation is unknown. A compound having the bond represented by the following bonding pattern is only an E form, only a Z form, or a mixture of an E form and a Z form.

Synthesis of Compound I-0001

Under nitrogen atmosphere, 2-(trimethylsilyl)ethanol (6.04 mL, 41.9 mmol) was dissolved in tetrahydrofuran (100 mL). Under ice cooling, sodium hydride (60% oil dispersion, 1.23 g, 30.7 mmol) was added to the solution. The mixture was stirred at room temperature for 30 minutes. Under ice cooling, the compound I (5.0 g, 27.9 mmol) in 50 mL of tetrahydrofuran solution was added dropwise to the mixture. The mixture was stirred at room temperature for 3 hours. 1 mol/L aqueous solution of hydrochloric acid was added to the mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by the saturated aqueous solution of sodium hydrogen carbonate and brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (hexane-ethyl acetate) to give the compound 2 (6.24 g, yield 85.7%).

1 H-NMR (CDCl 3 ) δ: 0.09 (s, 9H), 1.20 (t, J=8.0 Hz, 2H), 3.91 (s, 3H), 4.54 (t, J=8.0 Hz, 2H), 7.86 (s, 1H).

The compound 2 (1.0 g, 3.83 mmol) was dissolved in dioxane (10 mL). 3-chloro-2-methylaniline (760 mg, 5.37 mmol), bis(dibenzylideneacetone)palladium (220 mg, 0.383 mmol), Xantphos (333 mg, 0.575 mmol) and cesium carbonate (1.75 g, 5.37 mmol) were added to the solution. The mixture was stirred under reflux for 8 hours. Water was added to the mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (hexane-ethyl acetate) to give the compound 3 (1.1.5 g, yield 82.0%).

1 H-NMR (CDCl 3 ) δ: 0.07 (s, 9H), 1.19 (t, J=8.1 Hz, 2H), 2.38 (s, 3H), 3.84 (e, 3H), 4.47 (t, J=8.4 Hz, 2H), 6.58 (s, 1H), 7.08-7.10 (m, 2H), 7.79 (s, 1H), 7.87-7.95 (m, 1H).

The compound 3 (1.14 g, 3.12 mmol) was dissolved in tetrahydrofuran (5 mL). Tetrabutyl ammonium fluoride (1 mol/L tetrahydrofuran solution. 6.2 mL, 6.2 mmol) was added to the solution. The mixture was stirred at room temperature for 3 days. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (chloroform-methanol) to give the compound 4 (828 mg, yield 100%).

1 H-NMR (DMSO-d 6 ) δ: 2.25 (s, 3H), 3.64 (s, 3H), 7.13-7.40 (m, 3H), 7.67-7.82 (m, 1H), 7.90-8.11 (br, 1H), 11.20-11.06 (br, 1H).

Under nitrogen atmosphere), the compound 4 (53 mg, 0.199 mmol) was dissolved in a mixed solution of DMF (0.3 mL) and dimethoxyethane (1.5 mL). Sodium hydride (60% oil dispersion, 9 mg, 0.225 mmol) was added to the solution. The mixture was stirred at room temperature for 5 minutes. Then, lithium bromide (35 mg, 0.403 mmol) was added to the mixture. The mixture was stirred for 10 minutes, p-Fluorobenzyl bromide (50 μL, 0.402 mmol) was added to the mixture. The mixture was stirred at room temperature for 2 days. A 2 mol/L aqueous solution of hydrochloric acid was added to the mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by water, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (chloroform-methanol) to give the compound I-0001 (12 mg, yield 16.0%).

1 H-NMR (CDCl 3 ) δ: 2.06 (s, 3H), 3.71 (s, 3H), 5.01 (s, 2H), 6.66 (d, J=6.4 Hz, 1H), 6.80 (s, 1H), 7.04-7.15 (m, 4H), 7.32-7.40 (m, 2H), 7.63-7.61 (br, 1-H).

Synthesis of Compound I-0002

The compound I (40.0 g, 223 mmol) was dissolved in tetrahydrofuran (80 mL). A 1 mol/L aqueous solution of sodium hydroxide (447 mL, 447 mmol) was added to the solution. The mixture was stirred at room temperature for 4 hours. The reaction mixture was washed by ethyl ether. A 2 mol/L hydrochloric acid solution (230 mL, 400 mmol) was added to the aqueous layer. The mixture was stirred. The precipitates were filtered, washed by water, and dried to give the compound 5<30.8 g. yield 86%).

1 H-NMR (DMSO-d 6 ) δ: 3.70 (s, 3H), 7.60 (s, 1H)

The compound 5 (2.0 g, 12.46 mmol) was dissolved in dichloromethane (20 mL). DIEA (3.26 mL, 18.68 mmol) was added to the solution. The mixture was stirred until dissolved. Then, 3,5-difluorobenzyl bromide (1.91 mL, 14.95 mmol) was added to the mixture. The mixture was stirred at room temperature for 4 hours. After the mixture was left standing overnight, the precipited solids wore filtered, and dried to give the compound 6 (1.1 g, yield 31%).

1 H NMR (DMSO-d 6 ) δ: 3.70 (s, 3H), 5.30 (s, 2H), 7.05-7.13 (m, 2H), 7.82 (m, 1H)

The compound 6 (100 mg, 0.35 mmol) was dissolved in dioxane (2 mL). 3-chloro-2-methylaniline (74 mg, 0.52 mmol) was added to the solution. The mixture was stirred under microwave irradiation at 170° C. for 10 minutes. The solvent in the reaction mixture was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (ethyl acetate-n-hexane) to give the compound I-0002 (33 mg, yield 24%).

1 H-NMR (CDCl 3 ) δ: 2.05 (s, 3H), 3.73 (s, 3H), 5.01 (s, 2H), 6.65 (m, 1H), 6.75-6.95 (m, 4H), 7.05-7.15 (m, 2H), 7.59 (s, 1H)

Synthesis of Compound I-0003

The compound 7 (5 g, 41.6 mmol) was dissolved in concentrated sulfuric acid (35 mL). Under ice cooling, potassium nitrate (3.82 g, 37.8 mmol) dissolved in sulfuric acid (8 mL) was added to the solution. The mixture was stirred for 80 minutes. Water and ice were added to the reaction mixture. The precipited solids were filtered to give the compound 8 (5.68 g, yield 00%).

1 H-NMR (CDCl 3 ) δ: 5.18 (s, 4H), 7.89 (d, J=8.2 Hz, 1H), 8.11 (s, 1H), 8.18 (dd, J=8.3, 1.8 Hz, 1H).

The compound 8 (5.63 g, 34.1 mmol) was dissolved in ethanol (56 mL). Tin chloride dihydrate (23.1 g, 102 mmol) was added to the solution. The mixture was stirred at 70° C. for 1 hour. After cooled to room temperature, water and 2 mol/L aqueous solution of sodium hydroxide were added to the reaction mixture to adjust the pH to 7. The reaction mixture was extracted with ethyl acetate. The organic layer was washed by brine. The solvent was evaporated under reduced pressure to give the crude product of the compound 9 (4.6 g, yield 98%).

1 H-NMR (CDCl 3 ) δ: 8.71 (br s, 2H), 6.02 (s, 4H), 6.57 (s, 1H), 6.60 (dd, J=7.9, 2.0 Hz, 1H), 7.01 (d, J=7.9 Hz, 1H).

The compound 9 (7.5 g, 27.7 mmol) was dissolved in acetonitrile (90 mL). NBS (5.18 g, 29.1 mmol) was added to the solution at −10° C. The mixture was stirred at −10° C. for 30 minutes. Water was added to the reaction mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by water and brine. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (hexane-ethyl acetate) to give the mixture 10 (5:1 mixture of the compound 10-a and the compound 10-b) (3.68 g, yield 62%).

1 H-NMR (CDCl 3 ) δ: 4.08 (s, 2H), 4.98 (dd, J=7.8, 1.3 Hz, 4H), 6.61 (s, 1H), 7.28 (s, 1H).

The mixture 10 (3.68 g, 17.2 mmol) was dissolved in dioxane (86 mL) and water (7.2 mL). Trimethylboroxine (2.88 mL, 20.6 mmol), PdCl 2 (dppf) CH 2 Cl 2 (1.40 g, 1.72 mmol) and potassium carbonate (7.13 g, 51.6 mmol) were added to the solution. The mixture was stirred under reflux for 3 hours. Water was added to the reaction mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by water and brine. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (hexane-ethyl acetate). The obtained residue was solidified with ethyl acetate. The precipitated solids were filtered to afford the compound 11 (694 mg, yield 27%).

1 H-NMR (CDCl 3 ) δ: 2.18 (s, 3H), 3.62 (s, 2H), 5.01 (s, 4H), 6.56 (s, 1H), 6.92 (s, 1H).

The compound 11 (122 mg, 0.82 mmol) was dissolved in dioxane (4 mL). The compound 6 (21.3 mg, 0.74 mmol) was added to the solution. The mixture was stirred under microwave irradiation at 150° C. for 10 minutes. Water was added to the reaction mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by brine. The solvent, was evaporated. The obtained residue was purified by amino column chromatography (chloroform-methanol) to give the compound I-0003 (17 mg, yield 5%).

1 H-NMR (DMSO·D 6 ) δ: 3.59 (s, 3H), 4.94 (s, 4H), 5.20 (s, 2H), 7.01-7.03 (m, 3H), 7.11 (s, 1H), 7.24 (t, J=9.0 Hz, 1H), 7.34 (s, 1H), 8.36 (s, 1H).

Synthesis of Compound I-0004

The compound 5 (0.5 g, 8.11 mmol) was dissolved in dichloromethane (5 mL). DIEA (0.82 mL, 4.67 mmol) was added to the solution. The mixture was stirred until dissolved. Then, 3,4,5-trifluorobenzyl bromide (0.50 mL, 1.67 mmol) was added to the mixture. The mixture was stirred al room temperature for 1 hour. After the mixture was left standing overnight, the precipitated solids were filtered, and dried to give, the compound 12 (0.2 g, yield 22%).

1 H-NMR (DMSO-d 6 ) δ: 3.70 (s, 3H), 5.26 (s, 2H), 7.33-7.43 (m, 2H), 7.79 (s, 1H)

The compound 12 (100 mg, 0.35 mmol) was dissolved in dioxane (2 mL). 3-chloro-2-methylaniline (70 mg, 0.49 mmol) was added to the solution. The mixture was stirred under microwave irradiation at 170° C. for 10 minutes. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (ethyl acetate-n-hexane, subsequently chloroform-methanol-water) to give the compound I-0004 (47 mg, yield 35%).

1 H-NMR (DMSO-d 6 ) δ: 1.90 (s, 3H), 3.61 (s, 3H), 5.14 (brs, 2H), 6.90-7.60 (m, 7H)

Synthesis of Compound I-0005

The compound 5 (5 g, 31.1 mmol) was dissolved in dichloromethane (50 mL). DIEA (8.2 mL, 40.7 mmol) was added to the solution. The mixture was stirred until dissolved. Then, 3-chloro-4-fluorobenzyl bromide (5.03 mL, 37.4 mmol) was added to the mixture. The mixture was stirred at room temperature for 8 hours. After the mixture was left standing overnight, the precipitated solids were filtered, and dried to give the compound 13 (3.0 g, yield 32%).

1 H-NMR (DMSO-d 6 ) δ: 3.70 (s, 3H), 5.29 (s, 2H), 7.32-7.38 (m, 1H), 7.46 (t, 1H, J=8.9 Hz), 7.64 (1H, dd, J=7.0, 1.9 Hz), 7.84 (1H, s)

The compound 13 (250 mg, 0.83 mmol) was dissolved in dioxane (4 mL). The compound 14 (191 mg, 1.07 mmol) was added to the solution. The mixture was stirred under microwave irradiation at 150° C. for 20 minutes. Water was added to the reaction mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by brine. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (chloroform-methanol) to give the compound I-0005 (194 mg, yield 53%).

1 H-NMR (DMSO-D 6 ) δ: 1.95<s, 3H), 2.77 (s, 3H), 3.60 (s, 5H), 5.20 (s, 2H), 7.37 (s, 3H), 7.48 (s, 1H), 7.58 (s, 1H), 7.74 (s, 1H), 8.49 (s, 1H).

Synthesis of Compound I-0006

The compound 13 (100 mg, 0.330 mmol) was dissolved in dioxane (2.0 mL). 4-Chloro-2,5-dimethylaniline (103 mg, 0.660 mmol) was added to the solution. The mixture was stirred under microwave irradiation at 130° C. for 10 minutes. The solvent was evaporated under reduced pressure. The obtained residue was purified by reverse-phase silica-gel column chromatography (water-acetonitrile) to give the compound I-0006 (61.6 mg, yield 44%) as a white powder.

LC-MS (Condition [3]): RT=2.07, 422 [M+H]

1H-NMR (DMSO-D6) δ: 1.79 (3H, s), 2.26 (3H, s), 3.60 (3H, s), 5.17 (2H, br s), 6.95-7.55 (6H, m), 8.38 (1H, s).

Synthesis of Compound I-0007

The compound 5 (10 g, 62.3 mmol) was dissolved in dichloromethane (100 mL). DIEA (16.32 mL, 93 mmol) was added to the solution. The mixture was stirred until dissolved. Then, benzyl bromide (8.89 mL, 74.7 mmol) was added to the mixture. The mixture was stirred at room temperature for 3 hours. After the mixture was left, standing overnight, 2 mol/L aqueous solution of hydrochloric acid was added to the reaction mixture. The mixture was extracted with chloroform. The organic layer was washed by the saturated aqueous solution of sodium hydrogen carbonate and brine, and dried over anhydrous sodium sulfate. The obtained residue was solidified with ethyl acetate. The precipitated solids were filtered, and dried to give the compound 15 (8.42 g, yield 54%).

1 H-NMR (DMSO-D 6 ) δ: 1.95 (s, 3H), 2.77 (s, 8H), 3.60 (s, 5H), 5.20 (s, 2H), 7.37 (s, 3H), 7.48 (s, 1H), 7.58 (s, 1H), 7.74 (s, 1H), 8.49 (s, 1H).

Under nitrogen atmosphere, the compound 2 (80 mg, 0.319 mmol) was dissolved in dioxane (1.6 mL). 2-methyl-3-methoxyaniline (52.5 mg, 0.383 mmol), palladium acetate (2.85 mg, 0.013 mmol), Xantphos (11.04 mg, 0.019 mmol) and cesium carbonate (104 mg, 0.318 mmol) were added to the solution. The mixture was stirred under reflux for 5 hours. Water was added to the reaction mixture. The mixture was extracted with dichloromethane. The organic layer was washed by the saturated aqueous solution of ammonium chloride and brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (chloroform-methanol) to give the compound I-0007 (12.5 mg, yield 11%).

LC-MS (Condition (31): RT=1.53, 352 [M+H] +

1 H-NMR (DMSO-D 6 ) δ: 1.67 (s, 3H), 3.62 (s, 3H), 3.74 (s, 3H), 5.21 (s, 2H), 6.68 (1H, d, d=7.8 Hz), 6.84 (1H, d, J=8.3 Hz), 7.33-7.44 (m, 7H), 8.37 (s, 1H).

Synthesis of Compound I-0008

The compound 5 (300 mg, 1.87 mmol) was dissolved in dichloromethane (3 mL). DIEA (0.359 mL, 2.06 mmol) was added to the solution. The mixture was stirred until dissolved. Then, 2-bromoethylbenzene (380 mg, 2.06 mmol) was added to the mixture. The mixture was stirred at room temperature for 1.5 hours. After the mixture was left standing overnight, the reaction mixture was poured into water. The mixture was extracted with ethyl acetate. The organic layer was washed by brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (methanol-chloroform) to give the compound 16 (15.3 mg, yield 3%).

1 H-NMR (CDCl3) δ: 3.11 (t, 2H), 3.19 (s, 3H), 4.25 (t, 2H), 6.36 (s, 1H), 7.12-7.14 (m, 2H), 7.28-7.35 (m, 3H)

The compound 2 (1.5.0 mg, 0.057 mmol) was dissolved in dioxane (0.75 mL). 3-Chloro-2-methylaniline (16.0 mg, 0.113 mmol) was added to the solution. The mixture was stirred under microwave irradiation at 130° C. for 10 minutes. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (ethyl acetate-n-hexane) to give the compound I-0008 (13.1 mg, yield 63%).

1 H-NMR (CDCl3) δ; 3.12 (t, 2H), 2.22 (s, 3H), 3.48 (s, 3H), 4.07 (t, 2H), 6.30 (s, 1H), 6.67-6.69 (d, 2H), 7.09-7.12 (m, 2H), 7.21-7.23 (m, 2H), 7.26-7.28 (m, 1H), 7.28-7.36 (m, 2H), 7.53 (m, 1H)

Synthesis of Compound I-0009

The compound 17 (500 mg, 3.52 mmol) was dissolved in dichloromethane (5 mL). DIEA (921 μL, 5.28 mmol) and benzyl bromide (501 μL, 4.22 mmol) were added to the solution. The mixture was stirred at room temperature for 1 day. A 2 mol/L aqueous solution of hydrochloric acid was added to the mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (chloroform-methanol) to give the compound 18 (567 mg, yield (>9.4%).

1 H-NMR (CDCl 3 ) δ: 2.60 (s, 3H), 5.03 (s, 2H), 6.07 (d, J=7.6 Hz, 1H), 7.16-7.29 (m, 3H), 7.35-7.49 (m, 3H).

The compound 18 (0.100 mg, 0.430 mmol) was dissolved in tert-butanol (2 mL). Acetic acid (369 μL, 6.46 mmol) and 3-chloro-2-methylaniline (91 mg, 0.646 mmol) were added to the solution. The mixture was stirred under reflux for 33 hours. After cooled to room temperature, the mixture was diluted with ethyl acetate. The mixture was washed by the saturated aqueous solution of sodium hydrogen carbonate and brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (hexane-ethyl acetate) to give the compound I-0009 (65 mg, yield 46.3%).

1 H NMR (CDCl 3 ) δ: 2.03 (s, 3H), 5.07 (s, 2H), 5.43 (d, J=7.6 Hz, 1H), 6.68 (d, J=6.81 Hz, 1H), 7.05-7.13 (m, 2H), 7.20 (d, J=7.6 Hz, 1H), 7.32-7.49 (m, 6H).

Synthesis of Compound I-0010

The compound 19 (5.0 g, 29.9 mmol) was dissolved in tetrahydrofuran (10 mL). A 1 mol/L aqueous solution of sodium hydroxide (45 mL. 45.0 mmol) was added to the solution. The mixture was stirred at room temperature for 24 hours. The reaction mixture was washed by diethyl ether. Under ice cooling, 2 mol/L aqueous solution of hydrochloric acid was added to the mixture to adjust the pH to 3. The precipitated solids were filtered, and washed by cold water. The obtained solid was dried to give the compound 20 (2.5 g, yield 56.2%).

1 H-NMR (DMSO-d 6 ) δ: 8.15 (s, 1H).

The compound 20 (500 mg, 3.37 mmol) was dissolved in dichloromethane (5 mL). DIEA (882 μL, 5.05 mmol) and benzyl bromide (480 μL, 4.04 mmol) were added to the solution. The mixture was stirred al room temperature for 2 days. A 2 mol/L aqueous solution of hydrochloric acid was added to the mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (chloroform-methanol) to afford the compound 21 (331 mg, yield 41.2%).

1 H-NMR (CDCl 3 ) δ: 5.22 (s, 2H), 7.22-7.30 (m, 2H), 7.38-7.50 (m, 3H).

The compound 21 (100 mg, 0.419 mmol) was dissolved in dioxane (3 mL). 3-Chloro-2-methylaniline (71 mg, 0.501 mmol), palladium acetate (9 mg, 0.04 mmol), Xantphos (36 mg, 0.062 mmol) and cesium carbonate (191 mg, 0.587 mmol) were added to the solution. The mixture was stirred under microwave irradiation at 1.30° C. for 90 minutes. Water was added to the reaction mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (chloroform-methanol) to give the compound I-0010 (15 mg, yield 10.4%).

1 H-NMR (CDCl 3 ) δ: 2.06 (s, 3H), 5.04 (s, 2H), 6.67 (d, J=6.8 Hz, 1H), 7.06-7.65 (m, 911).

Synthesis of Compound I-0011

The compound 22 (7.2 g, 39.3 mmol) was dissolved in tetrahydrofuran (28 mL). A 1 mol/L aqueous solution of sodium hydroxide (56 mL, 56 mmol) was added to the solution. The mixture was stirred at room temperature for 1.5 hours. A 2 mol/L hydrochloric acid solution (6 mL, 12 mmol) was added to the mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by water and brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, Ethyl acetate-hexane was added to the obtained residue. The precipitated solids were filtered to give the compound 23 (3.4 g, yield 53%).

1 H-NMR (CDCl3) δ: 8.07 (s, 1H)

The compound 23 (3.0 g, 18.18 mmol) was dissolved in dichloromethane (30 mL). DIEA (4.76 mL, 27.30 mmol) was added to the solution. The mixture was stirred until dissolved. Then, benzyl bromide (2.34 mL, 20.00 mmol) was added to the mixture. The mixture was stirred at room temperature for 1.5 hours. After the mixture was left standing overnight, the reaction mixture was poured into water. The mixture was extracted with ethyl acetate. The organic layer was washed by 5% aqueous solution of citric acid and water, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. Ethyl ether was added to the obtained residue. The obtained solid was filtered to give the compound 24 (1.5 g, yield 32%).

1 H-NMR (CDCl3) δ: 5.22 (s, 2H), 7.20-7.30 (m, 2H), 7.40-7.50 (m, 3H), 7.58 (s, 1H)

The compound 24 (100 mg, 0.39 mmol) was dissolved in dioxane (2 mL). 3-Chloro-2-methylaniline (83 mg, 0.59 mmol) was added to the solution. The mixture was stirred under microwave irradiation at 130° C. for 10 minutes. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (ethyl acetate-n-hexane) to give the compound I-0011 (73 mg, yield 52%).

1 H-NMR (CDCl3) δ: 2.04 (s, 3H), 5.08 (s, 2H), 6.66 (d, J=7.2 Hz, 1H), 7.05-7.14 (m, 2H), 7.30-7.44 (m, 6H), 7.57 (s, 1H)

Synthesis of Compound I-0012

The compound 25 (5.0 g, 30.7 mmol) was dissolved in tetrahydrofuran (10 mL). A 1 mol/L aqueous solution of sodium hydroxide (46 mL, 46.0 mmol) was added to the solution. The mixture was stirred at room temperature for 24 hours. The reaction mixture was washed by diethyl ether. Under ice cooling, a 2 mol/L aqueous solution of hydrochloric acid was added to the mixture to adjust the pH to 3. The precipitated solids were filtered, and washed by cold water. The obtained solid was dried to give the compound 26 (1.9 g, yield 42.8%).

1 H-NMR (DMSO-d 6 ) δ: 1.96 (s, 3H), 7.94 (s, 1H), 12.80-13.80 (br, 1H).

The compound 26 (500 mg, 3.46 mmol) was dissolved in dichloromethane (5 mL). DIEA (904 μL, 0.19 mmol) and benzyl bromide (494 μL, 4.16 mmol) were added to the solution. The mixture was stirred at room temperature for 1 day. A 2 mol/L aqueous solution of hydrochloric acid was added to the mixture. The mixture was extracted with chloroform. The organic layer was washed by brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (chloroform-methanol) to give the compound 27 (416 mg, yield 51.2%). 41 NMR (CDCl 3 ) δ: 2.00 (s, 3H), 5.17 (s, 2H), 7.18-7.24 (m, 3H), 7.37-7.48 (m, 3H>.

The compound 27 (50 mg, 0.213 mmol) was dissolved in dioxane (3 mL). 3-Chloro-2-methylaniline (151 mg, 1.07 mmol) was added to the solution. The mixture was stirred under microwave irradiation at 100° C. for 120 minutes. Insoluble materials were filtered off, and rinced by ethyl acetate. The filtrate was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (hexane-ethyl acetate) to give the compound I-0012 (52 mg, yield 71.8%).

1 H-NMR (CDCl 3 ) δ: 1.86 (s, 3H), 2.04 (s, 3H), 5.05 (s, 2H), 6.67 (d, J=6.0 Hz, 1H), 7.02-7.12 (m, 3H), 7.32-7.43 (m, 5H), 7.46-7.52 (br, 1H).

Synthesis of Compound I-0013

Under nitrogen atmosphere, 2-(trimethylsilyl)ethanol (2.5 mL, 17.3 mmol) was dissolved in tetrahydrofuran (25 mL). Under ice cooling, sodium hydride (60% oil dispersion, 506 mg, 12.6 mmol) was added to the solution. The mixture was stirred at room temperature for 1 hour. Under ice cooling, the tetrahydrofuran solution (5 mL) of the compound 28 (2.0 g, 11.5 mmol) was added dropwise to the mixture. The mixture was stirred at room temperature for 5.5 hours. A 2 mol/L aqueous solution of hydrochloric acid was added to the mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel column chromatography (hexane-ethyl acetate) to give the compound 29<1.07 g, yield 36.4%).

1 H-NMR (CDCl 3 ) δ: 0.11 (s, 9H), 1.18-1.26 (m, 2H), 4.63-4.67 (m, 2H), 8.59 (s, 1H).

The compound 29 (693 mg, 2.71 mmol) was dissolved in dioxane (10 mL). 3-Chloro-2-methylaniline (537 mg, 3.79 mmol), palladium acetate (61 mg, 0.271 mmol), Xantphos (235 mg, 0.406 mmol) and cesium carbonate (1.24 g, 3.81 mmol) were added to the solution. The mixture was stirred under reflux for 1.5 hours. A 2 mol/L aqueous solution of hydrochloric acid was added to the mixture. The mixture was extracted with ethyl acetate. The organic layer was washed by the saturated aqueous solution of sodium hydrogen carbonate and brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica-gel