(en)Novel 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors which are useful as antihypercholesterolemic agents and are represented by the following general structural formulae (I) and (II): ##STR1## and pharmaceutically acceptable salts of the compounds (II) in which Z is hydrogen are disclosed.

1.ApplicationNumber: US-85952986-A
1.PublishNumber: US-4661483-A
2.Date Publish: 19870428
3.Inventor: HOFFMAN; WILLIAM F.
ROONEY; CLARENCE S.
LEE; TA J.

4.Inventor Harmonized: HOFFMAN WILLIAM F(US)
ROONEY CLARENCE S(US)
LEE TA J(US)

5.Country: US
6.Claims:
(en)Novel 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors which are useful as antihypercholesterolemic agents and are represented by the following general structural formulae (I) and (II): ##STR1## and pharmaceutically acceptable salts of the compounds (II) in which Z is hydrogen are disclosed.

7.Description:
(en)BACKGROUND OF THE INVENTION
Hypercholesterolemia is known to be one of the prime risk factors for ischemic cardiovascular disease such as arteriosclerosis. To date, there is still no effective antihypercholesterolemic agent commercially 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. The naturally occurring compounds and their semi-synthetic analogs have the following general structural formulae: ##STR2## wherein: Z is hydrogen, C 1-5 alkyl or C 1-5 alkyl substituted with a member of the group consisting of phenyl, dimethylamino, or acetylamino;
R is: ##STR3## wherein Q is ##STR4## R 2 is H or OH: R 1 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.
U.S. Pat. No. 4,517,373 discloses semi-synthetic compounds represented by the above general formula wherein R is ##STR5##
U.S. Pat. No. 4,346,227 and U.S. Pat. No. 4,448,979 also disclose semi-synthetic compounds represented by the above general formula wherein R is ##STR6##
Japanese unexamined patent application No. J59-122,483-A discloses a semi-synthetic compound represented by the above general formula wherein R is ##STR7## in which R 3 is hydrogen or methyl; R 4 is hydrogen, halogen or haloalkyl; R 5 is hydrogen, halogen or lower alkyl and R 6 is halogen, N 3 , hydroxy, thio, amino, loweralkoxy, lower alkylthio and aralkylthio.
U.S. Pat. No. 4,444,784 discloses 8'-acyloxy derivatives of compactin, mevinolin and the dihydro and tetrahydro analogs thereof. Generically disclosed are compounds represented by the above general formula wherein R is: ##STR8## in which R 7 is hydrogen or methyl and R 8 is C 1-10 alkyl, C 1-10 CF 3 substituted alkyl, phenyl-C 1-3 alkyl or substituted phenyl-C 1-3 alkyl in which the substituent is halo, C 1-3 alkyl or C 1-3 alkoxy.
SUMMARY OF THE INVENTION
This invention relates to novel compounds which are HMG-CoA reductase inhibitors and are useful as antihypercholesterolemic agents. Specifically, the compounds of this invention are semi-synthetic analogs of compactin, mevinolin, hydroxylated compactin and hydroxylated mevinolin and the dihydro and tetrahydro analogs thereof which possess a specifically substituted 8'-ester acyl moiety. Additionally, pharmaceutical compositions of these novel compounds, as the sole therapeutically active ingredient, and in combination with bile acid sequestrants are disclosed.
DETAILED DESCRIPTION OF THE INVENTION
The specific HMG-CoA reductase inhibitors of this invention are the compounds represented by the following general structural formulae (I) and (II): ##STR9## wherein: n is 0 to 5;
R 1 is C 1-3 alkyl;
R 2 is hydrogen or C 1-3 alkyl;
R 3 and R 4 independently are hydrogen, C 1-3 alkyl, C 3-7 cycloalkyl, phenyl or substituted phenyl in which the substituents are X and Y and when n is 2 to 5, each of the R 3 s and R 4 s are independently hydrogen or C 1-3 alkyl, c 3-7 cycloalkyl or only one of the R 3 s and R 4 s is phenyl or substituted phenyl;
R 5 is hydrogen or hydroxy;
R 6 and R 7 independently are hydrogen, or C 1-3 alkyl or R 6 and R 7 together with the nitrogen atom to which they are attached form a heterocycle selected from piperidinyl, morpholinyl, pyrrolidinyl, piperazinyl or thiomorpholinyl;
A is ##STR10## in which R 8 is hydrogen or hydroxy; B is ##STR11## which R 9 is hydrogen or hydroxy; a, b, c and d represent single bonds, one of a, b, c or d represents a double bond, or both a and c or both b and d represent double bonds provided that when a is a double bond, A is ##STR12## and when d is a double bond, B is ##STR13## and X and Y independently are hydrogen, halogen, trifluoromethyl, C 1-3 alkyl, nitro, cyano or a group selected from:
(a) R 10 O(CH 2 ) m in which m is 0 to 3 and R 10 is hydrogen, C 1-3 alkyl or hydroxy-C 1-3 alkyl;
(b) ##STR14## in which R 11 is hydrogen, C 1-3 alkyl, hydroxy-C 2-3 alkyl, phenyl, naphthyl, amino-C 2-3 alkyl, C 1-3 alkylamino-C 1-3 alkyl, di(C 1-3 alkyl)amino-C 1-3 alkyl, hydroxy-C 2-3 alkylamino-C 1-3 alkyl or di(hydroxy-C 2-3 alkyl)-amino-C 1-3 alkyl;
(c) ##STR15## in which R 12 is hydrogen, C 1-3 alkyl, hydroxy-C 1-3 -alkyl, C 1-3 alkoxy-C 1-3 alkyl, phenyl or naphthyl;
(d) R 13 R 14 N(CH 2 ) m , ##STR16## in which R 13 and R 14 independently are hydrogen, C 1-3 alkyl, hydroxy-C 2-3 alkyl or together with the nitrogen atom to which they are attached form a heterocycle group selected from piperidinyl, pyrrolidinyl, piperazinyl, morpholinyl or thiomorpholinyl;
(e) R 15 S(O) p (CH 2 ) m in which p is 0 to 2 and R 15 is hydrogen, C 1-3 alkyl, amino, C 1-3 alkylamino or di(C 1-3 alkyl)-amino;
Z is hydrogen, C 1-5 alkyl or C 1-5 alkyl substituted with a member of the group consisting of phenyl, dimethylamino or acetylamino;
and pharmaceutically acceptable salts of the compounds of the formula (II) in which Z is hydrogen.
Illustrative of one embodiment of this invention are the compounds of the formulae (I) and (II) wherein R 5 is hydrogen, R 8 is hydrogen, R 9 is hydrogen and a, b, c and d represent single bonds or both b and d represent double bonds. Specific compounds are those particular compounds wherein R 1 is methyl, R 2 is methyl, and R 3 and R 4 are hydrogen. Exemplifying this embodiment are the following compounds:
(1) 6(R)-[2-[8(S)-[3-(diethylamino)-2,2-dimethyl-3-oxopropionyloxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one;
(2) 6(R)-[2-[8(S)-(2,2-dimethyl-3-morpholino-3-oxopropionyloxy)-2(S),6(R)-dimethyl-1,2,-6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one;
(3) 6(R)-[2-[8(S)-[3-(dimethylamino)-2,2-dimethyl-3-oxopropionyloxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one;
(4) 6(R)-[2-[8(S)-[4-(dimethylamino)-2,2-dimethyl-4-oxobutanoyloxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one;
(5) 6(R)-[2-[8(S)-[2,2-dimethyl-3-(methylamino)-3-oxopropionyloxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one; and their corresponding free hydroxy acids.
Another embodiment of this invention is the class of compounds of the formula (II) wherein Z is hydrogen or C 1-5 alkyl and pharmaceutically acceptable salts of the compounds of the formula (II) wherein Z is hydrogen.
The pharmaceutically acceptable salts of this invention include those formed from cations such as sodium, potassium, aluminum, calcium, lithium, magnesium, zinc, and from bases such as ammonia, ethylenediamine, N-methyl-glucamine, lysine, arginine, ornithine, choline, N,N'-dibenzylethylenediamine, chloroprocaine, diethanolamine, procaine, N-benzylphenethylamine, diethylamine, piperazine, tris(hydroxymethyl)aminomethane, and tetramethylammonium hydroxide.
The compounds of formula (I) are conveniently prepared from compactin, mevinolin or the appropriate dihydro or tetrahydro analog thereof via the following general synthetic pathway: ##STR17##
The starting materials compactin, mevinolin, and their dihydro and tetrahydro analogs are readily available or may be prepared according to fermentation procedures disclosed in U.S. Pat. Nos. 3,983,140, 4,049,495, 4,231,938, 4,294,846, 4,343,814, and the hydrogenation procedures disclosed in U.S. Pat. No. 4,351,844. The appropriate starting material of formula (1) is then hydrolyzed under the conditions disclosed in U.S. Pat. No. 4,444,784 to afford the compounds of formula (2). The 4-hydroxy function in the lactone moiety of the compounds of formula (2) is protected with a suitable protecting agent, exemplified here as a dimethyl-t-butylsilyl group, according to the procedure disclosed in U.S. Pat. No. 4,444,784. Acylation of the 8' hydroxy group of the compounds of the formula (3) is accomplished under suitable conditions utilizing the appropriately substituted acids or acid halides of the formula (5) wherein n, R 1 , R 2 , R 3 , R 4 , R 6 and R 7 are as described above, and W is hydroxy, bromo or chloro. The protecting groups of the compound of formula (4 ) are removed utilizing suitable conditions to afford the compounds of the formula (I). For the compounds of this invention wherein the polyhydronaphthyl moiety is substituted with a hydroxy group, the compound of the formula (4) is subjected to a microbiological hydroxylation after the removal of the protecting groups utilizing the general procedures disclosed in U.S. Pat. Nos. 4,346,227, 4,448,979, 4,517,373 and Japanese Patent Application No. J-60-130,548.
The appropriately substituted acids or acid halides of the formula (5) are commercially available or prepared from known starting materials utilizing standard chemical transformations.
The compounds of the formula (II) wherein Z is hydrogen or a pharmaceutically acceptable salt thereof are readily prepared by the mild basic hydrolysis of the lactone moiety of the compounds of formula (I), careful acidification and formation of the appropriate salt utilizing standard procedures.
The compounds of the formula (II) wherein Z is C 1-5 alkyl or a substituted C 1-5 alkyl may be conveniently prepared by the procedures described in U.S. Pat. No. 4,342,767.
The compounds of this invention are useful as antihypercholesterolemic agents for the treatment of arteriosclerosis, hyperlipidemia, familial hypercholesterolemia and the like diseases in humans. They may be administered orally or parenterally in the form of a capsule, a tablet, an injectable preparation or the like. It is usually desirable to use the oral route. Doses may be varied, depending on the age, severity, body weight and other conditions of human patients but daily dosage for adults is within a range of from about 2 mg to 2000 mg (preferably 20 to 100 mg) which may be given in two to four divided doses. Higher doses may be favorably employed as required.
The compounds of this invention may also be coadministered with pharmaceutically acceptable nontoxic cationic polymers capable of binding bile acids in a non-reabsorbable form in the gastrointestinal tract. Examples of such polymers include cholestyramine, colestipol and poly[methyl-(3-trimethylaminopropyl)imino-trimethylene dihalide]. The relative amounts of the compounds of this invention and these polymers is between 1:1 and 1:15,000.
The intrinsic HMG-CoA reductase inhibition activity of the claimed compounds is measured in the in vitro protocol published in J. Med. Chem., 28, p. 347-358 (1985) and described below:
Isolation of HMG-CoA Reductase
Male Holtzman Sprague-Dawley rats (225-250 g) were kept on reversed lighting and fed Purina rat chow containing 3% cholestyramine for 7 days preceding their sacrifice by CO 2 asphyxiation. Livers were removed 6 hours into the dark cycle and used immediately to prepare microsomes. HMG-CoA reductase was solubilized from the freshly prepared microsome by the method of Heller and Shrewsbury [J. Biol. Chem., 1976, 251, 3815] and purified through the the second ammonium sulfate precipitation step as described by Kleinsek et al. [Proc. Natl. Acad. Sci. USA, 1977, 74, 1431]. The enzyme preparation was tested for HMG-CoA reductase potency and diluted with 100 mM phosphate buffer (pH 7.2) so that 100 μl of the enzyme solution, when added to the assay control, gave a value of 50,000-60,000 dpm. The enzyme preparation was stored at -80° C.
HMG-CoA Reductase Inhibition Assay
The assay is essentially the procedure of Shefer et al. [J. Lipid Res., 1972, 13, 402]. The complete assay medium contained the following in a total volume of 0.8 ml: phosphate buffer, pH 7.2, 100 mM; MgCl 2 , 3 mM; NADP, 3 mM; glucose 6-phosphate, 10 mM; glucose-6-phosphate dehydrogenase, 3 enzyme units; reduced glutathione, 50 mM; HMG-CoA (glutaryl-3- 14 C, New England Nuclear), 0.2 mM (0.1 μCi); and partially purified enzyme stock solution, 100 μL.
Test compounds or compactin (after first being converted to the sodium salt of their dihydroxy acid form in situ by addition of 1N NaOH (1 equivalent) were added to the assay system in 10-μL volumes at multiconcentration levels. After a 40-minute incubation at 37° C. with shaking and exposure to air, the reaction was stopped by the addition of 0.4 mL of 8N HCl. After an additional 30-minute incubation period at 37° C. to ensure the complete lactonization of mevalonic acid to mevalonolactone, 0.2 ml of the mixture was added to an 0.5×5.0 cm column containing 100-200 mesh Bio-Rex 5, chloride form (Bio-Rad), wetted with distilled water, as described by Alberts et al. [J. Proc. Natl. Acad. Sci. U.S.A., 1980, 77, 3957]. The unreacted [ 14 C]HMG-CoA was absorbed on the resin and the [ 14 C]mevalonolactone was eluted with distilled water (2×1 ml) directly into 7-ml scintillation vials. Five milliliters of Aquasol-2 (New England Nuclear) was added to each vial, and radioactivity was measured in a Packard Tri Carb Prias scintillation counter. IC 50 values were determined by plotting percentage inhibition against test compound concentration and fitting a straight line to the resulting data by using the least-squares method. For estimation of relative inhibitory potencies, compactin was assigned a value of 100 and the IC 50 value of the test compound was compared with that of compactin determined simultaneously.
Representative of the intrinsic HMG-CoA reductase inhibitory activities of the claimed compounds, tabulated below for a number of the claimed compounds are the relative potencies for said compounds.

TABLE 1______________________________________ ##STR18##T Relative Potency.sup.1______________________________________ ##STR19## 22 ##STR20## 20 ##STR21## 34 ##STR22## 16 ##STR23## 13______________________________________ .sup.1 Relative to compactin which was arbitrarily assigned a value of 10

Included within the scope of this invention is the method of treating arteriosclerosis, familial hypercholesterolemia or hyperlipidemia which comprises administering to a subject in need of such treatment a nontoxic therapeutically effective amount of the compounds of formulae (I) or (II) or pharmaceutical compositions thereof.


The following examples illustrate the preparation of the compounds of the formulae (I) and (II) and their incorporation into pharmaceutical compositions and as such are not to be considered as limiting the invention set forth in the claims appended hereto.
EXAMPLE 1
Preparation of 6(R)-[2-[8(S)-[3-(Diethylamino)-2,2-dimethyl-3-oxopropionyloxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one
(a) Methyl 2,2-dimethylmalonate (1a)
To a stirred solution of dimethyl 2,2-dimethylmalonate (22.1 g, 138 mmol) in methanol (40 ml) at aminent temperature was added dropwise a solution sodium hydroxide (5.52 g, 138 mmol) in water (20 ml). The reaction mixture was stirred for about 16 hours and then concentrated in vacuo at ambient temperature. The aqueous residue was cooled to 0°-5° C. and acidifed with 6N hydrochloric acid. The aqueous mixture was saturated with sodium chloride and extracted with diethyl ether (2×150 ml). The combined extracts were washed with saturated aqueous sodium chloride (2×100 ml), dried over magnesium sulfate and concentrated in vacuo to give a colorless oil. The oil was purified by distillation at 15 mmHg to give the desired product which solidified on cooling. mp 35°-38° C.
NMR(CDCl 3 ) δ=1.50 (6H, s), 3.78 (3H, s).
(b) Methyl 2,2-dimethylmalonyl chloride (1b)
To a stirred solution of the compound (1a) (5.0 g, 34.2 mmol) in dry benzene (25 ml) and dimethylformamide (2 drops) at ambient temperature was added oxalyl chloride (3.73 ml, 42.8 mmol). The reaction mixture was stirred for about 2 hours and the solvent removed in vacuo. The desired product was distilled at reduce pressure to yield a colorless liquid. bp 61°-62° C. at 15 mmHg.
NMR(CDCl 3 ) δ=1.56 (6H, s), 3.80 (3H, s).
(c) Methyl 3-(diethylamino)-2,2-dimethyl-3-oxoorooionate (1c)
To a stirred solution of freshly distilled compound (1b) (6.5 g, 39.5 mmol) in diethyl ether (100 ml) was added dropwise at ambient temperature a solution of freshly distilled diethylamine (6.35 g, 8.69 mmol) in diethyl ether (50 ml). The reaction mixture was stirred for 2 hours at ambient temperature and the diethylamine hydrochloride precipitate was removed by filtration. The filtrate was concentrated in vacuo to give a pale yellow oil. The oil was distilled at reduced pressure to give the desired product as a colorless liquid. bp 80°-82° C. at 0.3 mmHg.
NMR(CDCl 3 ) δ=1.11 (6H, t, J=7 Hz), 1.43 (6H, s), 3.14 (2H, m), 3.37 (2H, m), 3.73 (3H, s).
(d) 3-(Diethylamino)-2,2-dimethyl-3-oxopropionic acid (1d)
A stirred suspension of the compound (1c) (7.6 g, 37.8 mmol) in 1N sodium hydroxide (50 ml, 50 mmol) was heated at 70° C. for 5 hours and then cooled to 0°-5° C. The reaction mixture was acidified with concentrated hydrochloric acid (5 ml, 60 mmol) and a colorless solid crystallized. The solid was disolved in diethyl ether and organic phase dried over magnesium sulfate and concentrated in vacuo to give a colorless solid. The solid was recrystallized from diethyl ether/hexane to yield the desired product as colorless crystals. mp 110°-112° C.
Anal. Calc'd. for C 9 H 17 NO 3 : C, 57.73; H, 9.15; N, 7.48. Found: C, 58.09; H, 9.46; N, 7.19.
(e) 3-(Diethylamino)-2,2-dimethyl-3-oxopropionyl chloride (1e)
To a stirred suspension of the compound (1d) (6.6 g, 35.2 mmol) in benzene (25 ml) and freshly distilled oxalyl chloride (5.6 g, 44 mmol) was added at ambient temperature dimethylformamide (2 drops). After 1 hour at ambient temperature, additional dimethylformamide (2 drops) was added and the reaction mixture stirred for additional hour. The solvent was removed in vacuo to give a yellow liquid. The liquid was distilled at reduced pressure to give the desired product as a colorless liquid bp 74°-75° C. at 0.3 mmHg.
NMR(CDCl 3 ) δ=1.17 (6H, t, J=7 Hz), 1.55 (6H, s), 3.30 (4H, m).
(f) 6(R)-[2-[8(S)-[3-(Diethylamino)-2,2-dimethyl-3-oxopropionyloxy]2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-(dimethyl-tert-butylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one (1f)
To a stirred solution of 6(R)-[2-[8(S)-hydroxy-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-(tert-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one (1.08 g, 2.5 mmol) in dry pyridine (10 ml) containing 4-pyrrolidinopyridine (148 mg, 1 mmol) was added at 100° C. the compound (1e) (1.03 g, 5.0 mmol). After 3 hours additional compound (1e) (0.5 g) and 4-pyrrolidinylpyridine (148 mg) were added. After 8 hours additional compound (1e) (0.5 g) was added and reaction mixture heated at 100° C. for a total of 12 hours. The solvent was removed in vacuo and the residue partitioned between diethyl ether (200 ml) and water (25 ml) containing 6N hydrochloric acid (5 ml). The organic phase was washed with saturated aqueous sodium chloride (25 ml), saturated aqueous sodium bicarbonate (20 ml) and saturated aqueous sodium chloride (25 ml), dried over magnesium sulfate and concentrated in vacuo to give a reddish orange oil. The oil was chromatographed on a 3×15 cm column of silica gel eluted with 50 percent diethyl ether/hexane to afford the desired product as a viscous yellow oil.
NMR(CDCl 3 ) δ=0.01 (3H, s), 0.08 (3H, s), 0.87 (3H, d, J=7 Hz), 0.89 (9H, s), 1.03 (3H, d, J=7 Hz), 1.40 (6H, s), 3.22 (4H, m) 4.32 (H, m), 4.64 (H, m), 5.48 (H, m), 5.60 (H, m), 5.76 (H, dd, J=10 Hz, 6 Hz), 5.96 (H, d, J=10 Hz).
(g) 6(R)-[2-[8(S)-[3-(Diethylamino)-2,2-dimethyl-3-oxopropionyloxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a-(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one
To a stirred solution of the compound (1f) (1.5 g, 2.5 mmol) in tetrahydrofuran (20 ml) was added acetic acid (573 μl, 10 mmol) and tetra-n-butylammonium fluoride (7.5 ml, 1M in tetrahydrofuran, 7.5 mmol). The reaction mixture was heated at 70° C. for 3 hours. The reaction mixture was then cooled to ambient temperature and poured into diethyl ether (200 ml). The mixture was washed with water (25 ml) containing 6N hydrochloric acid (3 ml), saturated aqueous sodium chloride (25 ml), saturated aqueous sodium bicarbonate (2×25 ml) and saturated aqueous sodium chloride (25 ml), dried over magnesium sulfate and concentrated in vacuo to give a pale yelow oil. The oil was chromatographed on a 3×15 cm column of silica gel eluted with 25 percent acetone:methylene chloride (500 ml) and 30 percent acetone:methylene chloride to give the product as a colorless solid. mp 138°-140° C.
Anal. Calc'd. for C 28 H 43 NO 6 : C, 68.68; H, 8.85; N, 2.86. Found: C, 68.70; H, 8.93; N, 2.78.
NMR(CDCl 3 ) δ=0.89 (3H, d, J=7 Hz), 1.09 (3H, d, J=7 Hz), 1.12 (6H, m), 1.39 (3H, s), 1.42 (3H, s), 3.18 (4H, m), 4.38 (H, m), 4.60 (H, m), 5.49 (H, m), 5.57 (H, m), 5.68 (H, dd, J=10 Hz, 7 Hz), 5.98 (H, d, J=10 Hz).
EXAMPLE 2
Preparation of 6(R)-[2-[8(S)-(2,2-Dimethyl-3-morpholino-3-oxopropionyloxy)-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one
(a) Methyl 2,2-dimethyl-3-morpholino-3-oxoproprionate (2a)
Utilizing the general procedure of Example 1(c), the compound (1b) (5.76 g, 35 mmol) was reacted with freshly distilled morpholine (6.1 g, 70 mmol) to obtain the desired product as solid. mp 69°-71° C. Anal. Calc'd. for C 10 H 17 NO 4 : C, 55.80; H, 7.96; N, 6.51. Found C, 55.68; H, 8.20; N, 6.66.
(b) 2,2-Dimethyl-3-morpholino-3-oxopropionyl chloride (2b)
Utilizing the general procedures of Examples 1(d) and 1(e), the compound (2a) (6.9 g, 32 mmol) was converted into the desired product as viscous pale yellow liquid. bp 105°-107° C. at 0.3 mmHg.
NMR(CDCl 3 ) δ=1.50 (6H, s), 3.55 (4H, m), 3.71 (4H, m).
(c) 6(R)-[8(S)-(2,2-Dimethyl-3-morpholino-3-oxopropionyloxy)-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-(dimethyl-tert-butylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one (2c)
Utilizing the general procedure of Example 1(f), 6(R)-[2-[8(S)]-hydroxy-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-(tert-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one (1.08 g, 2.5 mmol) was reacted with the compound (2b) (1.09 g, 5.0 mmol) to yield the desired product as a colorless foam.
(d) 6(R)-[2[8(S)-(2,2-Dimethyl-3-morpholino-3-oxopropionyloxy)-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,-6-tetrahydro-2H-pyran-2-one
Utilizing the general procedure of Example 1(g), the compound (2c) (0.9 g, 1.46 mmol) was converted into the desired product as a colorless solid. mp 176°-179° C.
Anal. Calc'd. for C 28 H 41 NO 7 : C, 66.77; H, 8.21; N, 2.78. Found: C, 67.01; H, 8.23; N, 3.00.
NMR(CDCl 3 ) δ=0.88 (3H, d, J=7 Hz), 1.06 (3H, d, J=7 Hz), 1.41 (3H, s), 1.44 (3H, s), 3.41 (4H, m), 3.65 (4H, m), 4.38 (H, m), 4.62 (H, m) 5.49 (H, m), 5.58 (H, m), 5.80 (H, dd, J=10 Hz, 6 Hz), 5.97 (H, d, J=10 Hz).
EXAMPLE 3
Preparation of 6(R)-[2-[8(S)-[3-(Dimethylamino)-2,2-dimethyl-3-oxopropionyloxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one
Utilizing the general procedures of Example 1, the desired product was prepared from 6(R)-[2-[8(S)-hydroxy-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphythyl-1(S)]ethyl]-4(R)-(tert-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one (1.08 g, 2.5 mmol) and 3-(dimethylamino)-2,2-dimethyl-3oxopriopionyl chloride (0.888 g, 5.0 mmol) which was prepared from dimethylamine and the compound 1(b). The desired product was a colorless solid. mp 95°-97° C.
Anal. Calc'd. for C 26 H 39 NO 6 : C, 67.65; H, 8.52; N, 3.04. Found: C, 67.53; H, 8.77; N, 3.13.
NMR(CDCl 3 ) δ=0.90 (3H, d, J=7 Hz), 1.06 (3H, d, J=7 Hz), 1.44 (6H, s), 2.94 (6H, s), 4.41 (H, m), 4.64 (H, m), 5.48 (H,m), 5.64 (H, m), 5.80 (H, dd, J=10 Hz, 6 Hz) 5.99 (H, d, J=10 Hz).
EXAMPLE 4
Preparation of 6(R)-[2-[8(S)-[4-(Dimethylamino)-2,2-dimethyl-4-oxobutanoyloxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one
(a) 4-(Dimethylamino)-2,2-dimethyl-4-oxobutanoic acid (4a)
To a stirred solution of dimethylamine (6.8 g, 150 mmol) in tetrahydrofuran (150 ml) at 0° C. was added dropwise a solution of 2,2-dimethylsuccinic anhydride (4.8 g, 37.5 mmol) in tetrahydrofuran (50 ml) and reaction mixture stirred for about 16 hours at ambient temperature. The solvent was removed in vacuo and the residue was washed with 6N hydrochloric acid (5 ml) and methylene chloride was added to dissolve the precipitate. The solution was washed with saturated aqueous sodium chloride (2×25 ml), dried over magnesium sulfate and concentrated to a pale yellow solid. The solid was dissolved in methylene chloride (20 ml) and the desired product precipitated upon the addition of hexane to yield a colorless solid. mp 119°-121° C.
NMR(CDCl 3 ) δ=1.33 (6H, s), 2.64 (2H, s), 3.02 (3H, s), 3.07 (3H, s).
(b) 6(R)-[2-[8(S)-[4-(Dimethylamino)-2,2-dimethyl-4-oxobutanoyloxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a-hexahydronaphthyl-1(S)]ethyl]-4(R)-(dimethyl-tert-butylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one (4b)
To a stirred solution of the compound (4a) (0.866 g, 5 mmol) and N-methylmorpholine (550 μl, 5 mmol) in methylene chloride (10 ml) at -5° C. was added dropwise a solution of 2,4-dichloro-6-methoxytriazine (0.9 g, 5 mmol) in methylene chloride (10 ml). The reaction mixture was stirred for 2 hours under nitrogen at 0 to -10° C. To the reaction mixture was then added dropwise 6(R)-[2-[8(S)-hydroxy-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)ethyl-4(R)-(tert-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one (1.08 g, 2.5 mmol) in methylene chloride (10 ml) and the reaction mixture was heated to reflux. After 4 hours, a solution of the compound (4a) (0.433 g, 2.5 mmol) and 2,4 dichloro-6-methoxytriazine (0.45 g, 2.5 mmol) in methylene chloride (20 ml) was added. After another hour at reflux, additional compound (4a) (0.433 g, 2.5 mmol) and 2,4-dichloro-6-methoxytriazine (0.45 g, 2.5 mmol) was added and the reaction mixture refluxed for about 16 hours. The reaction mixture was cooled and poured into diethyl ether (200 ml). The mixture was washed with water (2×25 ml), 1N hydrochloric acid (10 ml), saturated aqueous sodium chloride (25 ml), saturated aqueous sodium bicarbonate (25 ml) and saturated aqueous sodium chloride (25 ml), dried over magnesium sulfate and concentrated in vacuo to give a viscous oil. The oil was chromatographed on a 5×15 cm column of silica gel eluted with 5 percent acetone/methylene chloride to yield the desired product as a colorless foam.
NMR(CDCl 3 ) δ=0.08(6H, s), 0.89(9H, s), 0.89(3H, d, J=7 Hz), 1.10(3H, d, J=7 Hz), 1.26(3H, s), 1.29(3H, s), 2.86(3H, s), 2.96(3H, s) 4.28(H, m), 4.57(H, m), 5.45(H, m) 5.49(H, m), 5.80(H, dd, J=10 Hz, 6 Hz), 5.98(H, d, J=10 Hz).
(c) 6(R)-[2-[8(S)-[4-(Dimethylamino)-2,2-dimethyl-4-oxobutanoyl]-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,-5,6-tetrahydro-2H-pyran-2-one
Utilizing the general procedure of Example 1(g), the compound (4b) (1.6 g, 2.5 mmol) was converted into the desired product as an amorphorous solid.
Anal. Calc'd. for C 27 H 41 NO 6 .1/2H 2 O: C, 66.91; H, 8.74; N, 2.89. Found: C, 67.30; H, 9.11; N, 3.03.
NMR(CDCl 3 ) δ=0.90(3H, d, J=7 Hz), 1.11(3H, d, J=7 Hz), 1.30(3H, s), 1.34(3H, s), 2.88(3H, s), 3.01(3H, s), 4.33(H, m), 4.62(H, m), 5.39(H, m), 5.51(H, m), 5.82(H, dd, J=10 Hz, 6 Hz), 6.00(H, d, J=10 Hz).
EXAMPLE 5
Preparation of 6(R)-[2-[8(S)-[2,2-dimethyl-3-(methylamino)-3-oxopropionyloxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one
Utilizing the general procedures of Example 1(a) through 1(d) and Example 4(b) and 4(c), the desired product was prepared from 6(R)-[2-[8(S)-hydroxy-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-(tert-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one (1.08 g, 2.5 mmol) and 2,2-dimethyl-3-(methylamino)-3-oxopropionic acid (0.726 g, 5 mmol) which was prepared from methylamine and the compound 1(b). The desired product was a colorless solid. mp 171°-773° C.
Anal. Calc'd. for C 25 H 37 NO 6 : C, 67.09; H, 8.33; N, 3.13. Found: C, 66.88; H, 8.39; N, 3.39.
NMR(CDCl 3 ) δ=0.89(3H, d, J=7 Hz), 1.06(3H, d, J=7 Hz), 1.43(3H, s), 1.45(3H, s), 2.89(3H, d, J=5 Hz) 4.36(H, m), 4.63(H, m), 5.37(H, m), 5.52(H, m), 5.80(H, dd, J=10 Hz, 6 Hz), 5.99(H, d, J=10 Hz).
EXAMPLE 6-20
Utilizing the general procedures of Example 1 the following compounds are prepared from the appropriately substituted acid chloride and compactin mevinolin and the dihydro and tetrahydro analogs thereof.

TABLE 2______________________________________ ##STR24##Compound T T.sub.1 b c d______________________________________ ##STR25## CH.sub.3 db -- db7 ##STR26## CH.sub.3 -- -- --8 ##STR27## H -- db --9 ##STR28## H -- -- --10 ##STR29## CH.sub.3 -- db --______________________________________


TABLE 3______________________________________ ##STR30##Com-pound T T.sub.1 T.sub.2 T.sub.3 a b c d______________________________________11 ##STR31## OH H H -- db -- db12 ##STR32## OH H H -- -- -- --13 ##STR33## H -- OH db -- db --14 ##STR34## CH.sub.3 -- OH db -- db --15 ##STR35## OH CH.sub.3 H -- db -- db______________________________________

EXAMPLE 16
Preparation of Alkali and Alkaline Earth Salts of Compound II
To a solution of the lactone from Example 1(g) (42 mg) in ethanol (2 ml) is added aqueous NaOH (1 equivalent). After one hour at room temperature, the mixture is taken to dryness in vacuo to yield the sodium salt of Compound II.
In like manner the potassium salt is prepared using one equivalent of potassium hydroxide, and the calcium salt using one equivalent of CaO.
EXAMPLE 17
Preparation of Methyl Ester of Compound II
To a solution of 400 mg of the lactone from Example 1(g) in 100 ml of absolute methanol is added 10 ml 0.1M sodium methoxide in absolute methanol. This solution is allowed to stand at room temperature for one hour, is then diluted with water and extracted twice with ethyl acetate; the ethyl acetate, dried over anhydrous sodium sulfate, is removed in vacuo to yield the methyl ester of Compound II.
In like manner, by the use of equivalent amounts of propanol, butanol, isobutanol, t-butanol, amyl alcohol, isoamyl alcohol, 2-dimethylaminoethanol, benzyl alcohol, phenethanol, 2-acetamidoethanol, and the like, the corresponding esters are obtained.
EXAMPLE 18
Preparation of Free Hydroxy Acids
The sodium salt of the compound II from Example 16 is redissolved in 2 ml of ethanol-water (1:1) and added to 10 ml of 1N hydrochloric acid from which the hydroxy acid is extracted with ethyl acetate. The latter solvent is washed once with water, dried, and removed in vacuo with a bath temperature not exceeding 30° C. The hydroxy acid derived slowly reverts to the lactone on standing.
EXAMPLE 19
As a specific embodiment of a composition of this invention, 20 mg of the lactone from Example 1(g) is formulated with sufficient finely divided lactose to provide a total amount of 580 to 590 mg to fill a size 0 hard gelatin capsule.