USRE33033E - Process for the preparation of HMG-CoA reductase inhibitors intermediates - Google Patents
Process for the preparation of HMG-CoA reductase inhibitors intermediates Download PDFInfo
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- USRE33033E USRE33033E US07/098,171 US9817187A USRE33033E US RE33033 E USRE33033 E US RE33033E US 9817187 A US9817187 A US 9817187A US RE33033 E USRE33033 E US RE33033E
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/732—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids of unsaturated hydroxy carboxylic acids
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
- C07C69/675—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids of saturated hydroxy-carboxylic acids
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
Definitions
- Hypercholesterolemia is known to be one of the prime etiological components of cardiovascular disease such as atherosclerosis, and there is still no effective antihypercholesterolemic agent available that has found wide patient acceptance.
- the bile acid sequestrants seem to be moderately effective but they must be consumed in large quantities, i.e. several grams at a time and they are not very palatable.
- agents known that are very active antihypercholesterolemic agents that function by limiting cholesterol biosynthesis by inhibiting the enzyme, HMG-CoA reductase.
- These agents include the natural fermentation products compactin and mevinolin and a variety of semi-synthetic and totally synthetic analogs thereof. These compounds have the following general structural formula: ##STR2## wherein R is ##STR3##
- This invention relates to a novel two step process for the preparation of the intermediate ester 2a in the synthesis of antihypercholesterolemic agents which contain a 4-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one moiety.
- the process involves the enantiomeric aldol condensation of an appropriately substituted aldehyde with the enolate of.Iaddend.with an alkyl acetate. resultant .[.enolate.].
- R is: ##STR9## wherein Q is ##STR10## R 5 is H or OH; R 6 is hydrogen or methyl; and a,b,c, and d represent optional double bonds, especially where b and d represent double bonds or a,b,c and d are all single bonds; or ##STR11## wherein E is --CH ⁇ CH-- or --CH 2 CH 2 --; and
- R 1 , R 2 and R 3 are each selected from halo such as chloro, bromo or fluoro,
- phenyl with one or more substituents independently selected from halo C 1-4 alkyl, and C 1-4 alkoxy, or
- R is the radical (A).
- Illustrative of this embodiment are the compounds of the formula I wherein R 5 is H, R 6 is H or CH 3 and b and d represent double bonds or a, b, c and d are all single bonds.
- R is the radical (B).
- R 1 is in the 6-position and represents phenyl with 1 or 2 substituents independently selected from chloro, fluoro, methyl and methoxy; and R 2 and R 3 are independently selected from halo and C 1-3 alkyl in the 2- and 4-positions.
- R is: ##STR14##
- the preparation of the compound of formula (IV) is accomplished by an aldol condensation of the appropriately substituted aldehyde with the enolate of.Iaddend.under standard aldol conditions as described in Braun et al., Tetrahedron Letters, Vol. 25, No. 44, pp 5031-5034 (1984). Specifically.Iaddend.is formed under anhydrous conditions in an aprotic solvent utilizing a non-nucleophilic base. Then the appropriately substituted aldehyde is added at low temperatures, between -100° C. and -30° C., preferrably -78° C. and the reaction allowed to go to completion.
- the preparation of the compound of the formula (I) is accomplished by a condensation of the compound of the formula (IV), with or without isolation, and with an enolate of a C 1-5 alkyl acetate.
- the compound of (IV) is isolated from the reaction mixture of the previous step, it is treated with between 2.0 and 3.0 equivalents, preferrably 2.5 equivalents, of a non-nucleophilic base, in an aprotic solvent, followed by the addition of the enolate of C 1-5 alkyl acetate which is formed in an aprotic solvent with a non-nucleophilic base.
- the compound of (IV) is not isolated the enolate of C 1-5 alkyl acetate is added directly to the reaction mixture of the previous step. This condensation is conducted at a temperature between 0° C. and -50° C., preferably -10° for a period of 30 minutes to 16 hours.
- non-nucleophilic bases which may be employed in both steps of this process are alkali metal amides of the formula:
- M + is a cation derived from sodium, potassium, lithium, magnesium or zinc and R 7 and R 8 independently are C 1-3 alkyl or when taken together with the nitrogen atom to which they are attached form a .Badd.5 or 6-membered heterocyclic ring and alkyl metals such as butyllithium.
- the preferred non-nucleophilic base is lithium diisopropylamide.
- the aprotic solvents that may be employed in both steps of this process are ethers, such as diethyl ether, tetrahydrofuran, 1,2-dimethoxyethane and the like.
- the preferred solvent is tetrahydrofuran.
- the reactions may conveniently be worked up by quenching with saturated ammonium chloride solution, and extracting into an organic solvent.
- R is the radical (A)
- the starting materials wherein R is the radical (B) are known in the art.
- Lithium diisopropylamide (6.65 mmol) was prepared by the addition of 4.75 ml of 1.4M n-butyllithium in hexanes to a solution of diisopropylamine (665 mg, 6.65 mmol) in 10 ml of tetrahydrofuran at -25° C. to -35° C. The mixture was stirred for 30 minutes at -25° C. and cooled to -78° C. t-Butylacetate (771 mg, 6.65 mmol) was added dropwise and the solution was stirred for 30 minutes at -78° C. and then warmed to -25° C. over 1 hour.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
.Iaddend.hypercholesterolemic compounds of the HMG-CoA reductase type of the following general formula (1): ##STR1## involving an enantioselective aldol condensation is disclosed.
Description
Hypercholesterolemia is known to be one of the prime etiological components of cardiovascular disease such as atherosclerosis, and there is still no effective antihypercholesterolemic agent available that has found wide patient acceptance. The bile acid sequestrants seem to be moderately effective but they must be consumed in large quantities, i.e. several grams at a time and they are not very palatable.
There are agents known, however, that are very active antihypercholesterolemic agents that function by limiting cholesterol biosynthesis by inhibiting the enzyme, HMG-CoA reductase. These agents include the natural fermentation products compactin and mevinolin and a variety of semi-synthetic and totally synthetic analogs thereof. These compounds have the following general structural formula: ##STR2## wherein R is ##STR3##
One group of totally synthetic analogs are disclosed in U.S. Pat. No. 4,375,475 and have the same general structural formula: ##STR4## wherein R is ##STR5## In the usual course of synthesis of these lactones an intermediate ester and dihydroxy acid are encountered: ##STR6## Each of these entities, as well as the lactone, demonstrate antihypercholesterolemic activity in vivo, of comparable magnitude. However, for these compounds to manifest a useful degree of activity, it.Iaddend. ve.ionship shown in the structures.[...].r .[.3R:5S/3S:5R.].
One of the prior art synthesis of these compounds comprises reduction of β-hydroxyketones 2a or 2b ##STR7## A stereoselective process for the reduction of β-hydroxyketones 2a.Iaddend.been described and disclosed in a copending U.S. patent application Ser. No. 725,891, filed Apr. 25, 1985.
This invention relates to a novel two step process for the preparation of the intermediate ester 2a in the synthesis of antihypercholesterolemic agents which contain a 4-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one moiety. The process involves the enantiomeric aldol condensation of an appropriately substituted aldehyde with the enolate of.Iaddend.with an alkyl acetate. resultant .[.enolate.].
A process for the preparation of a compound represented by the following general formula (I): ##STR8## wherein R is: ##STR9## wherein Q is ##STR10## R5 is H or OH; R6 is hydrogen or methyl; and a,b,c, and d represent optional double bonds, especially where b and d represent double bonds or a,b,c and d are all single bonds; or ##STR11## wherein E is --CH═CH-- or --CH2 CH2 --; and
R1, R2 and R3 are each selected from halo such as chloro, bromo or fluoro,
C1-4 alkyl,
C1-4 haloalkyl,
phenyl
phenyl with one or more substituents independently selected from halo C1-4 alkyl, and C1-4 alkoxy, or
R4 O in which R4 is phenyl, halophenyl, or
substituted phenyl-C1-3 alkyl wherein the substituents are selected from halo and C1-4 haloalkyl;
comprises:
(1) reacting a compound of the formula (II)
RCHO (II)
wherein R is defined above, with the enolate of.Iaddend.of the formula (III) riphenylethanol ##STR12## wherein M+ is a cation derived from sodium, potassium, lithium, magnesium or zinc, to afford a compound of the formula (IV) ##STR13## wherein R and M+ defined above; and
(2) reacting the compound of the formula (IV) with the enolate of a C1-5 alkylacetate, followed by mild acid hydrolysis to obtain the compounds of the formula (I).
In a first preferred embodiment R is the radical (A). Illustrative of this embodiment are the compounds of the formula I wherein R5 is H, R6 is H or CH3 and b and d represent double bonds or a, b, c and d are all single bonds.
In a second preferred embodiment, R is the radical (B). Illustrative of this embodiment are the compounds of the formula I wherein E is --CH═CH--, R1 is in the 6-position and represents phenyl with 1 or 2 substituents independently selected from chloro, fluoro, methyl and methoxy; and R2 and R3 are independently selected from halo and C1-3 alkyl in the 2- and 4-positions.
In the most preferred embodiment, R is: ##STR14##
The preparation of the compound of formula (IV) is accomplished by an aldol condensation of the appropriately substituted aldehyde with the enolate of.Iaddend.under standard aldol conditions as described in Braun et al., Tetrahedron Letters, Vol. 25, No. 44, pp 5031-5034 (1984). Specifically.Iaddend.is formed under anhydrous conditions in an aprotic solvent utilizing a non-nucleophilic base. Then the appropriately substituted aldehyde is added at low temperatures, between -100° C. and -30° C., preferrably -78° C. and the reaction allowed to go to completion.
The preparation of the compound of the formula (I) is accomplished by a condensation of the compound of the formula (IV), with or without isolation, and with an enolate of a C1-5 alkyl acetate. When the compound of (IV) is isolated from the reaction mixture of the previous step, it is treated with between 2.0 and 3.0 equivalents, preferrably 2.5 equivalents, of a non-nucleophilic base, in an aprotic solvent, followed by the addition of the enolate of C1-5 alkyl acetate which is formed in an aprotic solvent with a non-nucleophilic base. When the compound of (IV) is not isolated the enolate of C1-5 alkyl acetate is added directly to the reaction mixture of the previous step. This condensation is conducted at a temperature between 0° C. and -50° C., preferably -10° for a period of 30 minutes to 16 hours.
Illustrative of the non-nucleophilic bases which may be employed in both steps of this process are alkali metal amides of the formula:
M.sup.+ N.sup.- R.sup.7 R.sup.8 .8.].
wherein M+ is a cation derived from sodium, potassium, lithium, magnesium or zinc and R7 and R8 independently are C1-3 alkyl or when taken together with the nitrogen atom to which they are attached form a .Badd.5 or 6-membered heterocyclic ring and alkyl metals such as butyllithium. The preferred non-nucleophilic base is lithium diisopropylamide. Examples of the aprotic solvents that may be employed in both steps of this process are ethers, such as diethyl ether, tetrahydrofuran, 1,2-dimethoxyethane and the like. The preferred solvent is tetrahydrofuran.
The reactions may conveniently be worked up by quenching with saturated ammonium chloride solution, and extracting into an organic solvent.
The starting materials wherein R is the radical (A) may be prepared by using the synthetic methods described by HSU et al., J. Am. Chem. Soc., 1983, 105, pp. 593-601. The starting materials wherein R is the radical (B) are known in the art.
The following examples illustrate the present invention and as such are not to be considered as limiting the invention set forth in the claims appended hereto.
.[.To a suspension of (R)-2-acetoxy-1,2,2-triphenylethanol (332 mg, 1 .Iadd.To a suspension of (S)-2-acetyloxy-1,1,2-triphenylethanol (332 mg, 1 mmol), prepared according to the general procedure of Braun but.Iaddend.in tetrahydrofuran (2 ml) at -78° C. under nitrogen was added lithium diisopropylamide (prepared from 2.2 mmol of butyllithium and 2.42 mmol of diisopropylamine) in tetrahydrofuran (1 ml) and the reaction allowed to warm to 0° C. To the reaction mixture which was recooled to -78° C. was added E-3-(4'-fluoro-3,3',5-trimethyl[1,1'-biphenyl]-2-yl)-propenal in. After 30 minutes at -78° C. the reaction was quenched with a saturated solution of ammonium chloride. The desired product was extracted into ethyl acetate, dried over magnesium sulfate, and flash chromatographed over silica gel with hexane:ethylacetate(4:1) to give a yellow wax.
Lithium diisopropylamide (6.65 mmol) was prepared by the addition of 4.75 ml of 1.4M n-butyllithium in hexanes to a solution of diisopropylamine (665 mg, 6.65 mmol) in 10 ml of tetrahydrofuran at -25° C. to -35° C. The mixture was stirred for 30 minutes at -25° C. and cooled to -78° C. t-Butylacetate (771 mg, 6.65 mmol) was added dropwise and the solution was stirred for 30 minutes at -78° C. and then warmed to -25° C. over 1 hour. A solution of .[.(R)-2-[(E)-4-(4'-fluoro-3,3',5-trimethyl]1,1'-biphenyl]-2-yl]-3-hydroxy .Iadd.(S)-2-hydroxy-1,2,2-triphenylethyl(E)-5-(4'-fluoro-3,3',5-trimethyl-[.Iaddend.(800 mg, 1.33 mmol) in 2 ml tetrahydrofuran was added and the mixture was stirred for 1 hour at -25° C. and warmed to 22°-24° C. and stirred for 16 hours. The reaction mixture was quenched with a saturated solution of ammonium chloride and the product was extracted into methylene choride, dried over sodium sulfate and concentrated in vacuo to give the titled product.
.Iaddend.(166 mg, 0.5 mmol) in tetrahydrofuran (1 ml) at -78° C. under nitrogen was added lithium diisopropylamide (prepared from 1.2 mmol butyllithium and 1.2 mmol of diisopropylamine) in tetrahydrofuran (0.5 ml) and the reaction was allowed to warm to 0° C. To the reaction mixture which was recooled to -78° C. was added.Iaddend.-biphenyl]-2-yl)-propenal (132 mg, 0.5 mmol) in tetrahydrofuran (0.5 ml). After 30 minutes at -78° C., to the reaction mixture lithium tert butylacetate (prepared from tert butyl acetate 3.0 mmol, butyllithium 3.0 mmol and diisopropylamine 3.0 mmol) in tetrahydrofuran (3.0 ml) was added and the reaction mixture allowed to warm to -20° C. over 30 minutes. The mixture was then warmed to 22° and stirred.Iaddend.16 hours. The reaction was quenched with a saturated solution of ammonium chloride and the product extracted into methylene chloride. The organic phase was washed with saturated sodium chloride, dried over sodium sulfate and concentrated in vacuo to afford the above tilted product.
Utilizing the general procedures of Examples 1 and 2 or 3, the following compounds of the Formula I are prepared from the appropriate starting materials.
______________________________________
Compound
Number .[.R.sup.1.].tep .Iadd.R.Iaddend.
______________________________________
##STR15##
5
##STR16##
6
##STR17##
7
##STR18##
8
##STR19##
9
##STR20##
10
##STR21##
11
##STR22##
12
##STR23##
13
##STR24##
______________________________________
Claims (7)
1. A process for the preparation of a compound represented by the following general formula (I): ##STR25## wherein R is: ##STR26## wherein Q is ##STR27## R5 is H or OH;
R6 is hydrogen or methyl; and a, b, c, and d represent optional double bonds, especially where b and d represent double bonds or a, b, c and d are all single bonds; or ##STR28## wherein E is --C═CH-- or --CH2 CH2 --; and
R1, R2 and R3 are each selected from halo such as chloro, bromo or fluoro,
C1-4 alkyl,
C1-4 haloalkyl,
phenyl
phenyl with one or more substituents independently selected from halo,
C1-4 alkyl, and
C1-4 alkoxy, or
R4 O in which R4 is phenyl, halophenyl, or
substituted phenyl-C1-3 alkyl wherein the substituents are selected from halo and C1-4 haloalkyl;
which comprises:
(1) reacting a compound of the formula (II)
RCHO (II)
wherein R is defined above, with the enolate of .[.(R)-2-acetoxy-1,2,2-triphenylethanol.]. .Iadd.(S)-2-acetyloxy-1,1,2-triphenylethanol .Iaddend.of the formula (III) ##STR29## wherein M+ is a cation derived from sodium, potassium, lithium, magnesium, or zinc, to afford a compound of the formula (IV) ##STR30## wherein R and M+ are defined above; and (2) reacting the compound of the formula (IV) with the enolate of a C1-5 alkylacetate, followed by mild acid hydrolysis to obtain the compounds of the formula (I).
2. A process according to claim 1 wherein the compound of the formula (III) is prepared by treating .[.(R)-2-acetoxy-1,2,2-triphenylethanol.]. .Iadd.(S)-1-acetyloxy-1,1,2-triphenylethanol .Iaddend.with a non-nucleophilic base .[.employed to form the enolate of the compound of the formula (III) is an alkali metal amide of the formula:.]. .Iadd.of formula: .Iaddend.
M.sup.+ N.sup.- R.sup.7 R.sup.8
wherein M+ is a cation derived from sodium, potassium lithium, magnesium or zinc and R7 and R8 independently are C1-3 alkyl or when taken together with the nitrogen to which they are attached form a 5 or 6-membered heterocyclic ring.
3. A process according to claim 1 wherein the compound of the Formula (IV) is not isolated and the reactions are conducted in an aprotic solvent.
4. A process according to claim 1 wherein R is the radical (B).
5. A process according to claim 4 wherein E is --CH═CH--, R1 is in the 6-position and represents a phenyl with 1 or 2 substituents independently selected from chloro, fluoro, methyl and methoxy and R2 and R3 are independently selected from halo and C1-3 alkyl in the 2- and 4-position.
6. A process according to claim 5 for the preparation of C1-5 alkyl (E)-7-(4'-fluoro-3,3',5-trimethyl-[1,1 '-biphenyl]-2-yl)-3-oxo-5-hydroxy-6-heptenoate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/098,171 USRE33033E (en) | 1985-07-05 | 1987-09-18 | Process for the preparation of HMG-CoA reductase inhibitors intermediates |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/752,323 US4611081A (en) | 1985-07-05 | 1985-07-05 | Process for the preparation of HMG-CoA reductase inhibitors intermediates |
| US07/098,171 USRE33033E (en) | 1985-07-05 | 1987-09-18 | Process for the preparation of HMG-CoA reductase inhibitors intermediates |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/752,323 Reissue US4611081A (en) | 1985-07-05 | 1985-07-05 | Process for the preparation of HMG-CoA reductase inhibitors intermediates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE33033E true USRE33033E (en) | 1989-08-22 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/098,171 Expired - Fee Related USRE33033E (en) | 1985-07-05 | 1987-09-18 | Process for the preparation of HMG-CoA reductase inhibitors intermediates |
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| Country | Link |
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| US (1) | USRE33033E (en) |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4137322A (en) * | 1976-11-02 | 1979-01-30 | Sankyo Company Limited | ML-236B carboxylic acid derivatives and their use as antihyperlipemic agents |
| GB2055100A (en) * | 1979-07-27 | 1981-02-25 | Sankyo Co | Monacolin K derivatives |
| GB2075013A (en) * | 1980-04-22 | 1981-11-11 | Sankyo Co | Hydronaphthalene derivatives their preparation and use |
| GB2077264A (en) * | 1980-06-06 | 1981-12-16 | Sankyo Co | Ml-236b derivatives and their preparation |
| US4375475A (en) * | 1979-08-17 | 1983-03-01 | Merck & Co., Inc. | Substituted pyranone inhibitors of cholesterol synthesis |
| US4444784A (en) * | 1980-08-05 | 1984-04-24 | Merck & Co., Inc. | Antihypercholesterolemic compounds |
| US4447626A (en) * | 1981-07-21 | 1984-05-08 | Sankyo Company Limited | ML-236B Derivatives |
-
1987
- 1987-09-18 US US07/098,171 patent/USRE33033E/en not_active Expired - Fee Related
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4137322A (en) * | 1976-11-02 | 1979-01-30 | Sankyo Company Limited | ML-236B carboxylic acid derivatives and their use as antihyperlipemic agents |
| GB2055100A (en) * | 1979-07-27 | 1981-02-25 | Sankyo Co | Monacolin K derivatives |
| US4375475A (en) * | 1979-08-17 | 1983-03-01 | Merck & Co., Inc. | Substituted pyranone inhibitors of cholesterol synthesis |
| GB2075013A (en) * | 1980-04-22 | 1981-11-11 | Sankyo Co | Hydronaphthalene derivatives their preparation and use |
| US4438277A (en) * | 1980-04-22 | 1984-03-20 | Sankyo Company, Limited | Hydronaphthalene derivatives |
| GB2077264A (en) * | 1980-06-06 | 1981-12-16 | Sankyo Co | Ml-236b derivatives and their preparation |
| US4346227A (en) * | 1980-06-06 | 1982-08-24 | Sankyo Company, Limited | ML-236B Derivatives and their preparation |
| US4444784A (en) * | 1980-08-05 | 1984-04-24 | Merck & Co., Inc. | Antihypercholesterolemic compounds |
| US4447626A (en) * | 1981-07-21 | 1984-05-08 | Sankyo Company Limited | ML-236B Derivatives |
Non-Patent Citations (2)
| Title |
|---|
| J. E. Lynch, Tetrahedron Letters, 28, No. 13, 1385, (1987). * |
| M. Braun, Angew. Chem. Int. Ed., Engl., 26, 24, (1987). * |
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