Chiral derivatives of Garcinia acid bearing lactone ring moiety and process for preparing the same
Granted 3 Dec 2002 · 1 office action
Current assignee: MONKEYmedia, Inc. · originally DEPARTMENT OF MEDICAL SCIENCES
Law firm: Law firm · Log in to unlock
Attorney: Attorney · Log in to unlock
Inventors: Paleappadam Vavan Sasi, Grace Thomas, Ibrahim Ibnu Saud · Examiner: Amelia Owens · AU 1625 · TC 1600
Life of the application
10 dated eventsAbstract
The present invention relates to a novel chiral derivative of Garcinia acid bearing lactone ring moiety of formula I, wherein:R1R3alkali salt of carboxyl acid, or acid chloride or lower esters or part of N-substituted cyclic imides.R2hydroxyl or protected hydroxyl group and a process for preparing the same.
Description
8 parts›FIELD OF INVENTION
This invention relates to novel chiral derivatives bearing lactone moiety of Garcinia acid and a process for preparing the same.
›BACKGROUND OF THE INVENTION
Garcinia acid [(−)-Hydroxycitric acid lactone or (2S,3S)-Tetrahydro-3-hydroxy-5-oxo-2,3-furandicarboxylic acid] is isolated from the fruits of Garcinia cambogia, Garcinia indica and Garcinia atroviridis. Garcinia acid for formula Ia is widely used as an important ingredient in many pharmaceutical formulations 1-10 .
The non-availability of Ia in the market, in the pure form, has resulted in the limited use of these compounds in the area of organic synthesis and pharmaceutical front. This is due to the lack of any commercially viable large-scale manufacturing process. In U.S. patent application Ser. No.09/365,301,1999 an economic, commercially viable, cost effective process for the large-scale isolation of Ia has been described 11 .
Also during the past two decades there has been a great deal of interest to find cheap and potential chiral molecules from chiral pool to accomplish synthetic pathways with a high degree of asymmetric induction 12-25 .
Added to this, substituted γ-butyrolactones are known to be potent antagonists or agonists depending upon the substitution pattern of the γ-aminobutyric acid receptor, the major inhibitory neurotransmitter in the mammalian central nervous system 26 .
The known methods for obtaining diversity functionalised chiral γ-lactones are either by the cyclisation of acyclic starting materials such as the sterioselective iodolactonisation of unsaturated 3-hydroxy acids 27 or from sugars such as D-ribofiranose or D-glucosamine or carbohydrates such as D-ribose, D-glucose etc 28 . These chemical: modifications involving carbohydrates require tedious protocols.
›SUMMARY OF THE INVENTION
The object of this invention therefore is to prepare novel chiral derivatives of Garcinia acid and the process of preparing the same.
To achieve the objective this invention provides novel chiral derivatives of
Garcinia acid bearing lactone ring moiety of formula I-
wherein:
R 1 =R 3 =alkali salt of carboxyl acid, or acid chloride or part of N-substituted cyclic imides.
R 2 =hydroxyl or protected hydroxyl group.
In the above formula I
R 2 is —OH or protected hydroxyl group. To form various chiral derivatives of Garcinia acid bearing lactone ring moiety.
Chiral Derivatives of Garcinia Acid Bearing Lactone Ring Moiety
Summary of the chiral derivatives of Garcinia acid bearing lactone ring moiety is given below in scheme I:
The present invention further provides a process of preparation of Formula Ib comprising:
treating an aqueous solution of Ia with an aqueous solution of alkali till the pH of the solution is neutral,
evaporating the solution to dryness,
washing the residue with water miscible organic solvent,
drying the product Ib in vaccum.
The said alkali is sodium bicarbonate.
The invention further includes a process for the preparation of novel chiral derivative of formula Ic, comprising:
adding an organic halide to a suspension of Ib in organic solvent,
stirring the mixture for 1-4 hours,
filtering the said mixture,
evaporating the said solution to get Ic as a hygroscopic solid.
The said organic solvent is ether.
The said organic halide is thionyl chloride.
The invention further includes a process for the preparation of novel chiral derivative of formula Id comprising:
adding DMSO, an organic acid and an anhydride to If,
allowing the mixture to stand for 3-4days,
adding the reaction mixture to cold saturated aqueous solution of alkali,
stirring the mixture for 1-4 hours,
extracting the resultant solution with an organic solvent,
washing the extract with aqueous alkali,
drying the organic layer,
evaporating to get crude Id,
purifying the crude Id by chromatography to get pure Id as an yellow oil.
The said organic acid is acetic acid.
The said anhydride is acetic anhydride.
The said alkali is sodium bicarbonate.
The invention further includes a process of preparation of novel chiral derivative of formula Ig comprising:
refluxing the suspension of Ia in an organic halide for 3 hours,
concentrating the said mixture under vacuum,
dissolving the solid obtained in an organic solvent,
adding an appropriate amine to the dissolved solution,
stirring the mixture at room temperature for 4-18 hours,
concentrating the solution under vacuum,
adding the organic halide to the semi-solid obtained,
refluxing for 18 hours,
extracting with suitable organic solvent,
subjecting the said extract to chromatography furnishing Ig as white crystals.
The said organic halide is acetyl chloride.
The said appropriate amine is 4-methoxy benzyl amine.
The said organic solvent is chloroform.
The process will now be described with reference to the following examples.
›Examples5
›EXAMPLE 1
Garcinia Acid (Ia)
Dried rinds of the fruits of Garcinia cambogia (2.0 Kg) were cut into small pieces and soaked in hot water. The extract was collected after 20 hours and the process was repeated (4-5 times). The combined extract was concentrated to get a thick mass to which methanol was added. The precipitated pectin was filtered off and the filtrate was further concentrated to a syrup. The syrup was made alkaline by adding sufficient quantity of aqueous sodium hydroxide solution followed by the addition of methanol fill two layers separated. The separated sodium salt of Ia (lower layer) was washed several times with aqueous methanol. The pure sodium salt was dissolved in sufficient quantity of 2N hydrochloric, acid. To the concentrated solution acetone was added to remove insoluble impurities. The filtrate on concentration yielded crude crystals of Garcinia acid. Upon recrystallisation from acetone-chloroform mixture yielded crystals of Ia in high purity.
Melting point :178° C.
Yield: 135.0 g
›EXAMPLE 2
Disodium(2S,3S)-tetrahydro-3-hydroxy-5oxo-2,3-furandicarboxylate (Ib)
To an aqueous solution of Ia (2.0 g, 10.5 mmol, in 10 ml water) saturated sodium bicarbonate solution was added till the pH of the solution is neutral. The residue obtained after evaporation was washed with dry acetone (5×20 ml). The product Ib was finally dried under vacuum.
Yield: 2.0 g (82%).
›EXAMPLE 3
(2S,3S)-tetrahydro-3-hydroxy-5oxo2,3-furandicarbonylchloride (Ic)
To a suspension of Ib (1.0 g, 4.4 mmol) in ether (10 ml), thionyl chloride ( 1.0 ml, 14 mmol) was added. The mixture was stirred for two hours. Filtration followed by evaporation of the reaction mixture yielded Ic. Yield: 0.75 g (65%).
›EXAMPLE 4
Dimethyl(2S,3S)-tetrahydro3-oxo-[(methylthio)methoxy]-5ox-2,3-furandicarboxylate (Id)
To a solution of If (2 g, 9.2 mmol) in DMSO (28 ml), acetic acid (3.5 ml) in acetic anhydride (20 ml) was added. The mixture was allowed to stand for three days. The reaction mixture was added to saturated aqueous solution of sodium bicarbonate (400 ml) and stirred for one hour. It was extracted with chloroform (3×125 ml) and the combined chloroform extracts was washed: with saturated sodium bicarbonate solution (100 ml) followed by water (2×50 ml). The chloroform extract was dried (sodium sulphate) and evaporated to get crude Id (1.5 g). Id was further purified by column chromatography (silicagel 60-120 mesh, eluent: hexane-chloroform, 10-50%)
Yield: 0.75 g (29%)
›EXAMPLE 5
(3aS,6aS)-3a-(acetyloxy)dihydro5(phenylmethyl)6Hfuro[2,3-c]pyrrole-2,4,6 (3H,4H)-trione) (Ie)
A suspension of Ia (1g, 5 mmol) in acetyl chloride (4 ml) was refluxed for 3 hours followed by concentration under vacuum. The solid obtained was dissolved in THF (5 ml) and benzyl amine (0.535 ml, 5 mmol) was added. The mixture was stirred at room temperature for 4 hours and concentrated in vacuum. To the semi-solid obtained acetyl chloride (5 ml) was added and the mixture was refluxed for 18 hours. Extraction using ethyl acetate followed by recrystallisation from hexane—ethyl acetate furnished Ie as white crystals.
Melting point: 156-157° C.
Yield: 0.75 g. (52%)
Uses
Pharmaceutical applications
Chiral derivatives, Ia-Ig, are used as chiral synthons.
Claims as granted
21 claimsLog in to read the claims of this application.
Log in to unlockClassifications
5 codes- C07D307/33
- C07D491/048
- C07D491/04
Claim changes
SoonSee which claims were amended, added or cancelled during examination, with every added and removed word marked.
The published claims of this application are not paired with the granted ones in what we hold.
File wrapper
See the full prosecution history — every USPTO and applicant action on this file, in order.
Log in to unlockDocuments
Log in to open the documents of this file: the application as filed, every office action and response, the notice of allowance.
Log in to unlockChain of title
See the full assignment history — every owner this patent has passed through, with recordation dates and reel/frame numbers.
Log in to unlock