Novel chiral compounds derived from hexanoic acid esters, preparation process and intermediates, use in the synthesis of chiral 2-(bromomethyl)-2-ethylhexanoic acid

Abstract

A subject matter of the invention is a chiral compound of formula 1

Description

[0002] The present invention relates to novel chiral compounds derived from hexanoic acid esters, to their preparation process and intermediates, and to their use in the synthesis of chiral 2-(bromomethyl)-2-ethylhexanoic acid.

[0003] A subject matter of the invention is an (R) or (S) chiral compound corresponding to the formula (I) 2

[0004] in which R1 represents a hydroxyl radical or R′1, R′1 representing a group which activates the acid functional group, and R2 represents an alkyl radical including from 1 to 8 carbon atoms, optionally substituted by one or more halogen atoms, or a benzyl radical.

[0005] The term “alkyl radical including from 1 to 8 carbon atoms” is understood to mean any type of linear or branched alkyl and preferably a methyl, ethyl or propyl or butyl radical which is linear or branched.

[0006] The term “halogen atom” is understood to mean the fluorine, chlorine, bromine or iodine atom.

[0007] The term “alkyl radical substituted by halogen” is understood to mean a methyl radical or, preferably, an ethyl radical substituted by one or more chlorine or fluorine atoms. The term “group which activates the acid functional group” is understood to mean any group known to a person skilled in the art, for example a chlorine or bromine atom or an ester residue, for example derived from 1-hydroxybenzotriazole, a thioester residue, for example derived from 2-mercaptobenzothiazole, an amide residue, for example derived from benzotriazole 3-oxide, or a mixed anhydride residue, for example derived from sulfonates or phosphates.

[0008] Such groups are known in particular in acylation processes.

[0009] A subject matter of the invention is in particular a compound of formula (I) as defined above, in which R1 is chosen from the group consisting of a hydroxyl radical, a chlorine or bromine atom, a mixed anhydride residue, an activated thioester residue, an activated ester residue and an activated amide residue, and a compound of formula (I) as defined above, in which R2 is chosen from the group consisting of an alkyl radical including from 1 to 4 carbon atoms and a benzyl radical.

[0010] Another subject matter of the invention is a process for the preparation of the compounds of formula (I) as defined above, which comprises the treatment of a compound of formula (II) 3

[0011] in which R2 is defined as above, with a reactant capable of attaching a chain of formula 4

[0012] in which either A and B represent a hydrogen atom and C represents a bromine atom, or A and B form a second carbon-carbon bond and C represents a hydrogen atom, or A and C represent a hydrogen atom and B represents a ketone functional group, in order to obtain a compound of formula (III) 5

[0013] in which A, B, C and R2 have the abovementioned meanings, the ketone functional group of which B may represent being, if appropriate, protected in order to obtain a compound of formula (III′) 6

[0014] in which R2 has the abovementioned meaning and B′ represents a protected ketone functional group, then the treatment of the compound of formula (III) or (III′) with an enzyme having a hydrolytic activity, in order to obtain a chiral compound of formula (IV): 7

[0015] or a chiral compound of formula (IV1): 8

[0016] in which A, B, C and R2 have the abovementioned meanings, or a corresponding chiral compound of formula (IV′) or (IV′1) 9

[0017] in which B′ and R2 have the abovementioned meanings, which compound of formula (IV) or (IV1) or (IV′) or (IV′1) is treated with conditions capable of generating the corresponding chiral compound of formula (IA): 10

[0018] in which R2 has the abovementioned meaning, corresponding to a compound of formula (I) in which R1 is a hydroxyl radical, which compound, if appropriate, is treated with an agent which activates the acid functional group, in order to obtain a chiral compound of formula (IB) 11

[0019] in which R2 has the abovementioned meaning, corresponding to a compound of formula (I) in which R′1 has the abovementioned meaning.

[0020] The reactant capable of attaching the chain of formula —CH2—CHA—CHB—CH2C is a halogenated derivative of said chain or a derivative unsaturated at the chain end. Examples appear below in the experimental part.

[0021] The protection of the ketone functional group which B may represent can be any protection known to a person skilled in the art, for example a ketal or a thioketal.

[0022] The enzyme having a hydrolytic activity bringing about asymmetry can be in particular an esterase, a protease or a lipase, for example a hog liver esterase, chymotrypsin or a hog pancreas lipase. Mention may in particular be made, among the preferred enzymes, of the semipurified hog liver enzyme known under the trade name chirazyme E1.

[0023] The conditions capable of generating the chiral compound (IA) depend, of course, on the nature of the compound employed. If it is a compound in which A and B form a second bond or a compound in which C represents a bromine atom, a reduction is carried out, for example with hydrogen in the presence of palladium in tetrahydrofuran. If it is a compound in which B represents a ketone functional group, a reduction of Wolff-Kishner type is carried out, for example. If it is a ketal, a reduction with sodium in liquid ammonia can be carried out. If it is a thioketal, a reduction with hydrogen in the presence of a metal catalyst, in particular nickel, can be carried out.

[0024] The agent which activates the acid functional group is an agent capable of forming either an acid chloride or bromide, or an ester, or a thioester, or an amide, or a mixed anhydride. Such agents are conventional and known to a person skilled in the art, for example in carrying out an acylation reaction.

[0025] A further subject matter of the invention is the application of the compounds of formula (I) as defined above in the preparation of the chiral compound of formula (A): 12

[0026] which comprises subjecting a compound of formula (I) to the action of a reducing agent in order to obtain a chiral compound of formula (V): 13

[0027] in which R2 has the abovementioned meaning, which compound is saponified in order to obtain the chiral acid of formula (VI) 14

[0028] which compound is subjected to the action of a brominating agent in order to obtain the chiral compound of formula (A).

[0029] The reducing agent which is made to act on the compound (I) is, for example, an alkaline borohydride, such as sodium borohydride. It can also be an alkoxyborane or an acylborane.

[0030] The compound (I) used is preferably a compound in which R1 represents R′1.

[0031] The saponification of the compound of formula (V) can be carried out under conventional conditions known to a person skilled in the art.

[0032] The brominating agent is preferably hydrobromic acid.

[0033] The malonate derivative of formula (II) is known and described or can be prepared by described processes.

[0034] A final subject matter of the invention is the compounds of formula (III) and (III′) in which either A and B form a carbon-carbon bond and C represents a hydrogen atom, or A and C represent a hydrogen atom and B represents a ketone function, and B′ and R2 are as defined hereabove, the chiral compounds of formula (IV) and (IV1), (IV′) and (IV′1), and the chiral compounds of formula (V), (IV) and (A).

[0035] The compound of formula (A) is of use in particular in the synthesis of therapeutically active compounds.

[0036] The following examples illustrate the invention without, however, limiting it.

EXAMPLE 1

(2R)-2-Ethyl-2-(methoxycarbonyl)hexanoic acid

[0037] Stage A: Dimethyl 2-(4-bromobutyl)-2-ethylmalonate

[0038] 10.6 g of dimethyl 2-ethylmalonate, 57.4 g of 1,4-dibromobutane and 30 cm3 of tetrahydrofuran are mixed under an inert gas. The mixture is cooled to +3° C. and 8.5 g of potassium tert-butoxide in 55 cm3 of tetrahydrofuran are slowly introduced. After ¼ of an hour, the temperature is allowed to slowly rise and then the mixture is maintained at 25° C. with stirring for 3 h. It is poured into a mixture of 150 cm3 of water, 50 cm3 of methylene chloride and 5 cm3 of 2N hydrochloric acid, separation by settling is carried out and the organic phase is washed with water. The aqueous phases are reextracted with methylene chloride and the combined organic phases are dried and concentrated to dryness under reduced pressure. 62 g of an oil are obtained, which oil is distilled under a pressure of 1 mmHg. 16.2 g of the expected product are obtained.

[0039] NMR spectrum (CDCl3): 250 MHz 3.71 ppm OCH3 (6H, s), 3.42 ppm CH2Br (2H, t), 1.9 ppm CH2 (6H, m), 1.2 ppm CH2 (2H, m), 0.8 ppm CH3 (3H, t).

[0040] Stage B: (2R)-6-Bromo-2-ethyl-2-(methoxycarbonyl)hexanoic acid

[0041] 565 cm3 of water, 16.1 g of the product obtained in stage A and 28.5 cm3 of dimethyl sulfoxide are mixed, the mixture is heated to 30° C. and the pH is adjusted to 7 by addition of 1N sodium hydroxide solution. 5.4 g of chirazyme E1 are added. The mixture is stirred for 30 h at approximately 30° C. while maintaining the pH at 6.75 and then the enzyme is filtered off. The enzyme is washed on the filter by gradual addition of 170 cm3 of water. The aqueous phase thus obtained is basified by addition of 0.92 g of sodium bicarbonate. The enzyme and the aqueous phases are subsequently washed with methylene chloride. The combination of the combined aqueous phases is acidified to pH 2.7 by addition of 30 cm3 of 2N hydrochloric acid. Extraction is carried out with isopropyl ether, the organic phase is washed with water, dried and concentrated to dryness under reduced pressure, and 12.9 g of the expected product are obtained.

[0042] NMR spectrum (CDCl3) 250 MHz 3.79 ppm OCH3 (3H, s), 3.40 ppm CH2Br (2H, t), 2 ppm CH2 (6H, m), 1.4 ppm CH2 (2H, m), 0.8 ppm CH3 (3H, t). Ee=95% NMR CDCl3 in the presence of (R)-methylbenzylamine

[0043] Stage C: (2R)-2-Ethyl-2-(methoxycarbonyl)hexanoic acid

[0044] 12.44 g of the product obtained in stage B, 125 cm3 of tetrahydrofuran, 2.5 g of 10% palladium-on-charcoal and 12.5 cm3 of triethylamine are mixed. The mixture is placed under a hydrogen atmosphere and is kept stirred at approximately 26.° C. for 20 h. The catalyst is filtered off and is washed with tetrahydrofuran. The filtrate is concentrated to dryness under reduced pressure and the residue is taken up in 50 cm3 of isopropyl ether and 50 cm3 of water. The mixture is acidified by addition of 15 cm3 of 2N hydrochloric acid, separation by settling is carried out and the aqueous phase is reextracted with 50 cm3 of isopropyl ether. The combined organic phases are washed with water, dried and concentrated to dryness under reduced pressure. 8.91 g of the expected product are obtained.

[0045] NMR spectrum (CDCl3) 250 MHz 3.79 ppm OCH3 (3H, s), 2 ppm CH2 (4H, m), 1.2 ppm CH2 (4H, m), 0.8 ppm CH3 (6H, td).

EXAMPLE 2

Methyl (2S)-2-{[(diethoxyphosphoryl)oxy]carbonyl}-2-ethylhexanoate

[0046] 8.5 g of the product obtained in Example 1, 42.5 cm3 of methylene chloride and 8.5 cm3 of diethyl chlorophosphate are mixed under an inert gas. 6.3 g of 2,6-lutidine in 8.5 cm3 of methylene chloride are slowly introduced at approximately 25° C. After stirring for 18 h at approximately 25° C., 35 cm3 of methylene chloride and 42.5 cm3 of water are added. The addition is carried out for 5 min, the layers are separated by settling and then the organic phase is washed with water. The organic phase is dried and concentrated to dryness under reduced pressure, and 16.96 g of the expected product are obtained, which product is stored in solution in 10 cm3 of methylene chloride.

[0047] NMR spectrum (CDCl3) 250 MHz 4.3 ppm CH2 (4H, q), 3.8 ppm OCH3 (3H, s), 2 ppm CH2 (4H, m), 1.4 ppm CH2+CH3 (10H, q), 0.8 ppm CH3 (6H, t).

EXAMPLE 3

(2R)-2-Ethyl-2-(methoxycarbonyl)hexanoic acid

[0048] Stage A: Dimethyl 2-ethyl-2-(3-oxobutyl)malonate

[0049] 10 cm3 of dimethyl 2-ethylmalonate, 20 cm3 of methanol and 2.5 cm3 of methyl vinyl ketone are mixed under an inert gas. 7.5 cm3 of methyl vinyl ketone and 1 cm3 of 10% sodium methoxide in methanol are introduced over 1 h. The mixture is subsequently kept stirred at 26-27° C., is cooled to approximately 15° C. and then 2 cm3 of 1N hydrochloric acid and then 10 cm3 of water are added. The mixture is concentrated to half its volume, 90 cm3 of water are added and extraction is carried out with isopropyl ether. The organic phase is washed with water, dried and concentrated to dryness under reduced pressure, and 13.45 g of the expected product are obtained.

[0050] NMR spectrum (CDCl3) 250 MHz 3.8 ppm OCH3 (6H, s), 2.4 ppm CH2 (2H, t), 2.2 ppm CH2+CH3 (5H, t+s), 2 ppm CH2 (4H, q), 0.8 ppm CH3 (3H, t).

[0051] Stage B: (2R)-2-Ethyl-2-(methoxycarbonyl)-5-oxohexanoic acid

[0052] 20 cm3 of water, 0.504 g of the product obtained in stage A and 2 cm3 of dimethyl sulfoxide are mixed. The mixture is kept stirred at approximately 33-35° C. and then 0.25 g of chirazyme E1 is slowly added while maintaining the pH at 7-7.3 by addition of 0.5N sodium hydroxide solution. After 2 h, 10 cm3 of methylene chloride are added, acidification is carried out to a pH of 2 by addition of 3 cm3 of 1N hydrochloric acid, a further 10 cm3 of methylene chloride are added and separation is carried out by settling. The organic phase is washed with water, dried and concentrated to dryness under reduced pressure. 0.491 g of the expected product is obtained.

[0053] NMR spectrum (CDCl3) 250 MHz 3.8 ppm OCH3 (3H, s), 2.4 ppm CH2 (2H, t), 2.2 ppm CH2+CH3 (5H, t+s), 1.9 ppm CH2 (4H, q), 0.8 ppm CH3 (3H, t). Ee=96% NMR CDCl3 in the presence of (R)-methylbenzylamine

[0054] Stage C: (2R)-2-Ethyl-2-(methoxycarbonyl)hexanoic acid

[0055] 0.25 g of the product obtained in stage B is mixed with 0.23 g of NH2—NH—SO2—C6H4—CH3 and 2.5 ml of DMF. The mixture is left stirring for 2 hours and NaBH3CN, in solution in DMF (2 ml), is added over 1 hour. After stirring for 24 h, the product is isolated by running into 10% aqueous NaHCO3 solution and extraction is carried out in the presence of ethyl acetate to obtain, after concentrating, 0.2 g of the expected product.

[0056] NMR spectrum (CDCl3) 250 MHz 3.79 ppm OCH3 (3H, s), 2 ppm CH2 (4H, m), 1.2 ppm CH2 (4H, m), 0.8 ppm CH3 (6H, td).

EXAMPLE 4

(2R)-2-Ethyl-2-(methoxycarbonyl)hexanoic acid

[0057] Stage A: Dimethyl 2-ethyl-2-[2-(2-methyl-1,3-dithiolan-2-yl)ethyl]malonate

[0058] 4.65 g of the product obtained in stage A of Example 3 and 23 cm3 of toluene are mixed at 20-22° C. under an inert gas. 3.7 g of ethanedithiol and 4.25 g of boron trifluoride etherate are added over 10 min at approximately 23° C. After stirring for 17 h at ambient temperature, the reaction mixture is poured into a mixture of 50 cm3 of isopropyl ether and 50 cm3 of a water/ice mixture. Stirring is carried out for 5 min, separation by settling is carried out, the aqueous phase is reextracted with isopropyl ether and the combined organic phases are washed with water and with a 1% aqueous sodium bicarbonate solution. They are dried and concentrated to dryness under reduced pressure, and 6.64 g of the expected product are obtained.

[0059] NMR spectrum (CDCl3) 250 MHz 3.8 ppm OCH3 (6H, s), 3.3 ppm S—CH2—CH2—S (4H, m), 2.2 ppm CH2—S (2H, m), 2 ppm CH2 (2H, q), 1.8 ppm CH2+CH3 (5H, m+s), 0.9 ppm (3H, t).

[0060] Stage B: (2R)-2-Ethyl-2-(methoxycarbonyl)-4-(2-methyl-1,3-dithiolan-2-yl)butanoic acid

[0061] 6 cm3 of water, 0.124 g of the product obtained in stage A and 0.6 cm3 of dimethyl sulfoxide are mixed. 0.125 g of chirazyme E1 is slowly added while maintaining the temperature at 33-34° C. and the pH at 7.5-8.5 by addition of 0.2N sodium hydroxide solution. The reaction mixture is kept stirred for 26 h and then 6 cm3 of methylene chloride and 0.6 cm3 of 1N hydrochloric acid are added. The mixture is separated by settling, the aqueous phase is reextracted with methylene chloride and the organic phases are combined, washed with water, dried and concentrated to dryness under reduced pressure. 0.107 g of the expected product is obtained.

[0062] NMR spectrum (CDCl3) 250 MHz 3.8 ppm OCH3 (3H, s), 3.3 ppm S—CH2—CH2—S (4H, m), 2.2 ppm CH2—S (2H, m), 2 ppm CH2 (2H, q), 1.8 ppm CH2+CH3 (5H, m+s), 0.9 ppm (3H, t). Ee=95% NMR CDCl3 in the presence of (R)-methylbenzylamine

[0063] Stage C: (2R)-2-Ethyl-2-(methoxycarbonyl)hexanoic acid

[0064] 0.107 g of the product obtained in stage B, 1 cm3 of tetrahydrofuran and 25 mg of nickel are mixed. The mixture is placed under a hydrogen atmosphere and is kept stirred at approximately 26.° C. for 20 h. The catalyst is filtered off and is washed with tetrahydrofuran. The filtrate is concentrated to dryness under reduced pressure and the residue is taken up in 10 cm3 of isopropyl ether and 10 cm3 of water. Separation by settling is carried out and the aqueous phase is reextracted with 10 cm3 of isopropyl ether. The combined organic phases are washed with water, dried and concentrated to dryness under reduced pressure. 0.5 g of the expected product is obtained.

[0065] NMR spectrum (CDCl3) 250 MHz 3.79 ppm OCH3 (3H, s), 2 ppm CH2 (4H, m), 1.2 ppm CH2 (4H, m), 0.8 ppm CH3 (6H, td).

EXAMPLE 5

(2R)-2-Ethyl-2-(methoxycarbonyl)hexanoic acid

[0066] Stage A: Dimethyl 2-ethyl-2-[2-(2-methyl-1,3-dioxolan-2-yl)ethyl]malonate

[0067] 0.45 cm3 of ethylene glycol, 10 mg of para-toluenesulfonic acid and 0.88 cm3 of methyl orthoformate are mixed and then 0.92 g of the product obtained in stage A of Example 3 is added. The mixture is kept stirred for 24 h at ambient temperature and is then poured into 20 cm3 of a 1% aqueous sodium bicarbonate solution. Extraction is carried out with methylene chloride and the organic phase is washed with water, dried and concentrated to dryness under reduced pressure. 1.6 g of the expected product are obtained.

[0068] NMR spectrum (CDCl3) 250 MHz 4 ppm O—CH2—CH2—O— (4H, s), 3.75 ppm OCH3 (6H, s), 2 ppm CH2 (4H, m), 1.5 ppm CH2 (2H, m), 1.4 ppm CH3 (3H, s), 0.9 ppm (3H, t).

[0069] Stage B: (2R)-2-Ethyl-2-(methoxycarbonyl)-4-(2-methyl-1,3-dioxolan-2-yl)butanoic acid

[0070] 20 cm3 of water, 0.55 g of the product obtained in stage A and 2 cm3 of dimethyl sulfoxide are mixed, the mixture is kept stirred at 30-32° C. and then 0.266 g of chirazyme E1 is slowly added while maintaining the temperature at approximately 33° C. and the pH at 7.2-7.5 by addition of 0.5N sodium hydroxide solution. After 24 h, the temperature is brought back to 20° C. and then 10 cm3 of methylene chloride are added. The mixture is acidified by addition of 2.3 cm3 of 1N hydrochloric acid and separated by settling, and the organic phase is washed with water, dried and concentrated to dryness under reduced pressure. 0.452 g of the crude expected product is obtained.

[0071] NMR spectrum (CDCl3) 250 MHz 4 ppm O—CH2—CH2—O— (4H, s), 3.8 ppm OCH3 (6H, s), 2 ppm CH2 (4H, m), 1.6 ppm CH2 (2H, m), 1.4 ppm CH3 (3H, s), 0.9 ppm CH3 (3H, t). Ee=99% NMR CDCl3 in the presence of (R)-methylbenzylamine

[0072] Stage C: (2R)-2-Ethyl-2-(methoxycarbonyl)hexanoic acid

[0073] 0.4 g of the product obtained in stage B is mixed in 8 ml of liquid NH3 at −70° C. with 0.22 mg of Na. The temperature is maintained at −70° C. for 3 h. An NH4Cl solution (2 ml) is added over 1 h at −30° C. and extraction is carried out with ethyl acetate. The organic phase is washed with water, dried and concentrated to dryness under reduced pressure. 0.31 g of the expected product is obtained.

[0074] NMR spectrum (CDCl3) 250 MHz 3.79 ppm OCH3 (3H, s), 2 ppm CH2 (4H, m), 1.2 ppm CH2 (4H, m), 0.8 ppm CH3 (6H, td).

EXAMPLE 6

(2R)-2-Ethyl-2-(methoxycarbonyl)hexanoic acid

[0075] Stage A: Dimethyl (2E)-2-[but-2-enyl]-2-ethylmalonate

[0076] 10 cm3 of dimethyl 2-ethylmalonate, 20 cm3 of DMF and 1.27 g of NaH are mixed at 0° C. under an inert gas. 5.8 g of 4-chloro-2-butene are introduced over 1 h while maintaining the temperature at 0° C. After reacting for 2 h at 0° C., 10 ml of 1N HCl are introduced, the mixture is then concentrated, 10 ml of water are added and extraction is carried out with isopropyl ether. After drying the extract, 8.2 g (E/Z 85/15) of an oil are recovered.

[0077] NMR spectrum (CDCl3) 250 MHz 4.6 ppm vinyl H (H, td), 4.2 ppm vinyl H (H, q), 3.75 ppm OCH3 (6H, s), 2.5 ppm CH2 (2H, dd), 2.4 ppm CH3 (3H, d), 1.4 ppm CH2 (2H, q), 0.9 ppm (3H, t).

[0078] Stage B: (2R,4E)-2-Ethyl-2-(methoxycarbonyl)hex-4-enoic acid

[0079] 8 g of the product obtained in stage A are mixed. 8 g of chirazyme E1 are slowly added while maintaining the temperature at approximately 33° C. and the pH at 6.88 by addition of 1N sodium hydroxide solution. After 24 h, extraction is carried out with methylene chloride and the organic phase is washed with water, dried and concentrated to dryness under reduced pressure. 6.8 g of the expected product are obtained.

[0080] NMR spectrum (CDCl3) 250 MHz 4.6 ppm vinyl H (H, td), 4.2 ppm vinyl H (H, q), 3.70 ppm OCH3 (3H, s), 2.6 ppm CH2 (2H, dd), 2.5 ppm CH3 (3H, d), 1.5 ppm CH2 (2H, q), 0.9 ppm (3H, t). Ee=26% NMR CDCl3 in the presence of (R)-methylbenzylamine

[0081] Stage C: (2R)-2-Ethyl-2-(methoxycarbonyl)hexanoic acid

[0082] 6 g of the product obtained in stage B, 60 cm3 of tetrahydrofuran, 1.25 g of 10% palladium-on-charcoal and 6.25 cm3 of triethylamine are mixed. The mixture is placed under a hydrogen atmosphere and is kept stirred at approximately 26.° C. for 20 h. The catalyst is filtered off and is washed with tetrahydrofuran. The filtrate is concentrated to dryness under reduced pressure and the residue is taken up in 25 cm3 of isopropyl ether and 25 cm3 of water. The mixture is acidified by addition of 7 cm3 of 2N hydrochloric acid, separation by settling is carried out and the aqueous phase is reextracted with 25 cm3 of isopropyl ether. The combined organic phases are washed with water, dried and concentrated to dryness under reduced pressure. 5.7 g of the expected product are obtained.

[0083] NMR spectrum (CDCl3) 250 MHz 3.79 ppm OCH3 (3H, s), 2 ppm CH2 (4H, m), 1.2 ppm CH2 (4H, m), 0.8 ppm CH3 (6H, td).

EXAMPLE 7

(2S)-2-(Bromomethyl)-2-ethylhexanoic acid

[0084] Stage A: Methyl (2R)-2-ethyl-2-(hydroxymethyl)hexanoate

[0085] 27.4 g of the mixed anhydride solution obtained in Example 2 are concentrated to 16 g and then 53 cm3 of dimethylformamide are added thereto with stirring and under an inert gas. The mixture is cooled to approximately +2° C. and then 1.75 g of sodium borohydride are slowly added. 1 h 45 min after the end of the introduction, a further 0.17 g of sodium borohydride is added and then, 1 h later, a further 0.17 g of sodium borohydride is again added. 73 cm3 of isopropyl ether are subsequently added and then 35 cm3 of a 5% aqueous tartaric acid solution are added at 6-10° C. over 15 min. After stirring for 5 min, the mixture is separated by settling, the aqueous phase is reextracted with isopropyl ether and then the combined organic phases are washed with a saturated aqueous sodium bicarbonate solution and then with water. They are dried and concentrated to dryness under reduced pressure, and 7.3 g of the crude expected product are obtained, which product is chromatographed on silica, elution being carried out with a heptane/ethyl acetate 7/3 mixture. 7.2 g of the purified product are obtained.

[0086] NMR spectrum (CDCl3) 250 MHz 3.79 ppm OCH3 (3H, s), 3.69 ppm CH2OH (2H, s), 2 ppm CH2 (4H, m), 1.2 ppm CH2 (4H, m), 0.8 ppm CH3 (6H, td).

[0087] Stage B: (2R)-2-Ethyl-2-(hydroxymethyl)hexanoic acid

[0088] 7 g of the product obtained in stage A are dissolved in 70 ml of methanol, and 37 ml of 1N sodium hydroxide solution are added at 0° C. The mixture is maintained at 0° C. for 1 h; the medium is concentrated, the residue is taken up in 37 ml of 1N HCl and the expected product is extracted with 2×50 ml of ethyl acetate. 5.6 g of the expected product are obtained.

[0089] NMR spectrum (CDCl3) 250 MHz 3.69 ppm CH2OH (2H, s), 1.6 ppm CH2 (4H, m), 1.2 ppm CH2 (4H, m), 0.8 ppm CH3 (6H, td).

[0090] Stage C: (2S)-2-(Bromomethyl)-2-ethylhexanoic acid

[0091] 5.6 g of the product obtained as described in stage B and 34.8 cm3 of 62% hydrobromic acid are mixed, the mixture is then brought to 92° C.±2° C. with stirring for 7 hours and then it is left standing for 16 hours at 20° C. The mixture is cooled to 0° C. and 60 cm3 of water and then 9.8 cm3 of 32% sodium hydroxide solution are added. The mixture is kept stirred and 25 cm3 of toluene are introduced, then 50 cm3 of water and 50 cm3 of toluene are again introduced and the mixture is stirred for 1 hour at 20° C. The mixture is separated by settling, the aqueous phase is reextracted with toluene and the organic phases are combined, dried and concentrated to dryness under reduced pressure. 6.1 g of the crude expected product are obtained, which product is purified by distillation under 2 mmHg. 3.17 g of the expected product are obtained (Bp2=118-124° C.).

[0092] NMR spectrum (CDCl3) 250 MHz 3.52 ppm CH2Br (2H, s), 1.6 ppm CH2 (4H, m), 1.2 ppm CH2 (4H, m), 0.8 ppm CH3 (6H, td). αD(20) (1% CHCl3)=+40°

Claims

1. A (R) or (S) chiral compound of the formula (I)

2. The compound of formula (I) as defined in claim 1, wherein R1 is chosen from the group consisting of hydroxyl, chlorine or bromine, a mixed anhydride residue, an activated thioester residue, an activated ester residue and an activated amide residue.

3. The compound of formula (I) as defined in claim 1, wherein R2 is chosen from the group consisting of C1-C4-alkyl and a benzyl radical.

4. A process for the preparation of the compounds of formula (I) as defined in claim 1, comprising: treating a compound of formula (II) 16 wherein R2 is as defined in claim 1, with a reactant capable of attaching a chain of formula 17 wherein either A and B is hydrogen and C is bromine, or A and B form a second carbon-carbon bond and C is hydrogen, or A and C each is hydrogen and B is a ketone functional group, in order to obtain a compound of formula (III) 18 wherein A, B, C and R2 have the abovementioned meanings, the ketone functional group of which B may represent is optionally protected in order to obtain a compound of formula (III′) 19 wherein R2 has the abovementioned meaning and B′ is a protected ketone functional group; treating the compound of formula (III) or (III′) with an enzyme having a hydrolytic activity, in order to obtain a chiral compound of formula (IV): 20 or a chiral compound of formula (IV1): 21 wherein A, B, C and R2 have the abovementioned meanings, or a corresponding compound of formula (IV′) or (IV′1) 22 wherein B′ and R2 have the abovementioned meanings; treating compound of formula (IV) or (IV1) or (IV′) or (IV′1) under conditions capable of generating the corresponding chiral compound of formula (IA) 23 wherein R2 has the abovementioned meaning, corresponding to a compound of formula (I) wherein R1 is hydroxyl; and optionally treating a compound of formula (IA)with an agent which activates the acid functional group, in order to obtain a chiral compound of formula (IB) 24 wherein R2 has the abovementioned meaning, corresponding to a compound of formula (I) in which R′1 is defined as in claim 1.

5. A process for the preparation of the chiral compound of formula (A):

6. The process of claim 5 wherein R1 of formula (I) is R′1.

7. A compound selected from the group consisting of:

8. A chiral compound selected from the group consisting of:

9. A chiral compound selected from the group consisting of:

10. A chiral compound of formula (A):