Perhydro-1,4-thiazepin-5-one and perhydro-1,4-thiazocin-5-one derivatives as antihypertensives

Claim 2

A compound of the formula: ##STR125## wherein R and R 3 are independently hydrogen, C 1 -C 6 alkyl, aryl, and aralkyl; R 1 is hydrogen; hydrocarbon of from 1 to 12 carbon atoms which include branched, cyclic and unsaturated hydrocarbon groups; substituted C 1 -C 6 alkyl wherein the substituent can be halo, hydroxy, carboxy, lower alkylthio, lower alkoxy, lower alkoxy carbonyl, lower aralkoxy carbonyl, amino, lower alkylamino, diloweralkylamino, or acylamino; substituted C 1 -C 6 alkyl having the formula R A (CH 2 ) n --Q--(CH 2 ) m wherein n is 0-2, m is 1-3, R A is aryl or heteroaryl optionally substituted by amino, diloweralkylamino, lower alkylamino, hydroxy, hydroxy loweralkyl, aminoloweralkyl, trihaloloweralkyl, cyano, nitro, sulfonamido, aroyl, lower alkyl, halo, dihalo, and lower alkoxy, and Q is O, S, N--R B , CONR C , NR C CO, CH═CH wherein R B is hydrogen, loweralkyl, aryl, aralkyl, lower alkanoyl, or aroyl, and R C is hydrogen or lower alkyl; aryl; substituted aryl wherein the substituent is lower alkyl, amino loweralkyl, loweralkoxy, aryloxy, aroyl, hydroxy, halo, or dihalo; aralkyl or heteroaralkyl which include branched lower alkyl groups; substituted aralkyl or substituted heteroaralkyl which include branched lower alkyl groups wherein the lower alkyl groups can be substituted by amino, acylamino, or hydroxyl and the aryl and heteroaryl groups can be substituted by halo, dihalo, loweralkyl, hydroxy, loweralkoxy, aryloxy, aroyl, arylthio, amino, amino lower alkyl, lower alkanoylamino, aroylamino, diloweralkylamino, lower alkylamino, hydroxy loweralkyl, trihalo loweralkyl, nitro, cyano, or sulfonamido; R 2 is hydrogen or loweralkyl; n is 1 or 2; p is 0 or 1; X is oxygen; and, the pharmaceutically acceptable salts thereof, wherein in said R-R 3 groups, unless otherwise stated, the loweralkyl groups contain from one to six carbon atoms; aryl and the prefix "ar" represent phenyl, naphthyl or biphenyl; the aralkyl and heteroaralkyl groups contain from one to six carbon atoms in the alkyl portion thereof and represent benzyl, phenethyl, 3,3-diphenylpropyl, or 3-indolylmethyl; heteroaryl represents indolyl, thienyl, imidazolyl, furyl, benzimidazolyl, pyridyl, quinolinyl, isoquinolinyl, and benzothienyl; aroyl denotes benzoyl or 1-naphthoyl; acylamino denotes loweralkanoylamino and aroylamino which are selected from the group consisting of acetylamino, and benzoylamino; and, alkoxy denotes a loweralkyl group bonded to oxygen.

Claim 3

A compound of claim 1 wherein: R and R 3 are hydrogen, loweralkyl, aryl or aralkyl; R 1 is a hydrocarbon of 1-10 carbon atoms which include branched, cyclic and unsaturated hydrocarbon groups; substituted loweralkyl wherein the substituent can be hydroxy, lower alkylthio, amino, alkylamino, diloweralkylamino, and acylamino; substituted lower alkyl having the formula R A (CH 2 ) n --Q--(CH 2 ) m -- wherein n is 0-2, m is 1-3, R A is aryl or heteroaryl optionally substituted by alkyl, halo, dihalo, amino, cyano, hydroxy, or alkoxy, and Q is O, S, N--R B , CONR C , NR C CO, or CH═CH wherein R B is hydrogen, lower alkyl, aralkyl, lower alkanoyl, or aroyl and R is hydrogen or lower alkyl; aralkyl or heteroaralkyl which include branched lower alkyl groups; R 2 is hydrogen or lower alkyl; n is 1 or 2; and, p is 0.

Claim 4

A compound of claim 2 wherein n is 1.

Claim 5

A compound of claim 3 wherein: R and R 3 are independently hydrogen, lower alkyl of 1 to 4 carbon atoms, phenyl, or benzyl; R 2 is hydrogen or lower alkyl R 1 is alkyl of 1-8 carbon atoms which include branched alkyl groups; substituted lower alkyl wherein the substituent can be amino or loweralkylthio; substituted lower alkyl having the formula R A (CH 2 ) n --Q--(CH 2 ) m -- wherein n is O, m is 1, R A is phenyl, and Q is O or S; aralkyl wherein the aryl is phenyl or naphthyl and the alkyl group contains 1 to 3 carbon atoms, or heteroaralkyl wherein the heteroaryl group is indole, thiophene, imidazole, pyridine, quinoline or isoquinoline and the alkyl group contains 1 to 3 carbon atoms; substituted aralkyl wherein the aryl is phenyl, the alkyl contains 1 to 3 carbon atoms, and the substituents can be halo, hydroxy, phenoxy, lower alkoxy, amino, or aminomethyl, and, R 2 is hydrogen, loweralkyl.

Claim 6

A compound which has the formula: ##STR126##

Claim 7

A compound which has the formula: ##STR126##

Claim 8

The compound of claim 5 which is: 4-N-(1(S)-carboxyethyl)-6(R)-(1(S)-carboethoxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one.

Claim 9

A compound which has the formula: ##STR127##

Claim 10

A compound which has the formula: ##STR127##

Claim 11

The compound of claim 7 which is: 4-N-(1(S)-carboxyethyl)-6(R)-(1(S)-carboxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one.

Claim 12

A compound which has the formula: ##STR128##

Claim 13

A compound which has the formula: ##STR128##

Claim 14

The compound of claim 9 which is: 4-N-carboxymethyl-6(R)-(1(S)-carboethoxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one.

Claim 15

A compound which has the formula: ##STR129##

Claim 16

A compound which has the formula: ##STR129##

Claim 17

The compound of claim 11 which is: 4-N-carboxymethyl-6(R)-(1(S)-carboxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one.

Claim 18

A pharmaceutical composition useful in the treatment of hypertension which comprises a pharmaceutically acceptable carrier and an antihypertensively effective amount of a compound of the formula: ##STR130## wherein R and R 3 are independently hydrogen, C 1 -C 6 alkyl, aryl, and aralkyl; R 1 is hydrogen; hydrocarbon of from 1 to 12 carbon atoms which include branched, cyclic and straight chain hydrocarbon groups; substituted C 1 -C 6 alkyl wherein the substituent can be halo, hydroxy, carboxy, lower alkylthio, lower alkoxy, lower alkoxy carbonyl, lower aralkoxy carbonyl, amino, lower alkylamino, diloweralkylamino, or acylamino; substituted C 1 -C 6 alkyl having the formula R A (CH 2 ) n --Q--(CH 2 ) m wherein n is 0-2, m is 1-3, R A is aryl or heteroaryl optionally substituted by amino, diloweralkylamino, lower alkylamino, hydroxy, hydroxy loweralkyl, aminoloweralkyl, trihaloloweralkyl, cyano, nitro, sulfonamido, aroyl, lower alkyl, halo, dihalo, and lower alkoxy, and Q is O, S, N--R B , CONR C , NR C CO, CH═CH wherein R B is hydrogen, loweralkyl, aryl, aralkyl, lower alkanoyl, or aroyl, and R C is hydrogen or lower alkyl; aryl; substituted aryl wherein the substituent is lower alkyl, amino loweralkyl, loweralkoxy, aryloxy, aroyl, hydroxy, halo, or dihalo; aralkyl or heteroaralkyl which include branched lower alkyl groups; substituted aralkyl or substituted heteroaralkyl which include branched lower alkyl groups wherein the lower alkyl groups can be substituted by amino, acylamino, or hydroxyl and the aryl and heteroaryl groups can be substituted by halo, dihalo, loweralkyl, hydroxy, loweralkoxy, aryloxy, aroyl, arylthio, amino, amino lower alkyl, lower alkanoylamino, aroylamino, diloweralkylamino, lower alkylamino, hydroxy loweralkyl, trihalo loweralkyl, nitro, cyano, or sulfonamido; R 2 is hydrogen or loweralkyl; n is 1 or 2; p is --or 1; X is oxygen; and, the pharmaceutically acceptable salts thereof, wherein in said R-R 3 groups, unless otherwise stated, the loweralkyl groups contain from one to six carbon atoms; aryl and the prefix "ar" represent phenyl, naphthyl or biphenyl; the aralkyl and heteroaralkyl groups contain from one to six carbon atoms in the alkyl portion thereof and represent benzyl, phenethyl, 3,3-diphenylpropyl, or 3-indolylmethyl; heteroaryl represents indolyl, thienyl, imidazolyl, furyl, benzimidazolyl, pyridyl, quinolinyl, isoquinolinyl, and benzothienyl; aroyl denotes benzoyl or 1-naphthoyl; acylamino denotes loweralkanoylamino and aroylamino which are selected from the group consisting of acetylamino, and benzoylamino; and, alkoxy denotes a loweralkyl group bonded to oxygen.

Claim 19

A pharmaceutical composition useful in the treatment of hypertension which comprises a pharmaceutically acceptable carrier and an antihypertensively effective amount of a compound of the formula: ##STR130## wherein R and R 3 are independently hydrogen, C 1 -C 6 alkyl, aryl, and aralkyl; R 1 is hydrogen; hydrocarbon of from 1 to 12 carbon atoms which include branched, cyclic and straight chain hydrocarbon groups; substituted C 1 -C 6 alkyl wherein the substituent can be halo, hydroxy, carboxy, lower alkylthio, lower alkoxy, lower alkoxy carbonyl, lower aralkoxy carbonyl, amino, lower alkylamino, diloweralkylamino, or acylamino; substituted C 1 -C 6 alkyl having the formula R A (CH 2 ) n --Q--(CH 2 ) m wherein n is 0-2, m is 1-3, R A is aryl or heteroaryl optionally substituted by amino, diloweralkylamino, lower alkylamino, hydroxy, hydroxy loweralkyl, aminoloweralkyl, trihaloloweralkyl, cyano, nitro, sulfonamido, aroyl, lower alkyl, halo, dihalo, and lower alkoxy, and Q is O, S, N--R B , CONR C , NR C CO, CH═CH wherein R B is hydrogen, loweralkyl, aryl, aralkyl, lower alkanoyl, or aroyl, and R C is hydrogen or lower alkyl; aryl; substituted aryl wherein the substituent is lower alkyl, amino loweralkyl, loweralkoxy, aryloxy, aroyl, hydroxy, halo, or dihalo; aralkyl or heteroaralkyl which include branched lower alkyl groups; substituted aralkyl or substituted heteroaralkyl which include branched lower alkyl groups wherein the lower alkyl groups can be substituted by amino, acylamino, or hydroxyl and the aryl and heteroaryl groups can be substituted by halo, dihalo, loweralkyl, hydroxy, loweralkoxy, aryloxy, aroyl, arylthio, amino, amino lower alkyl, lower alkanoylamino, aroylamino, diloweralkylamino, lower alkylamino, hydroxy loweralkyl, trihalo loweralkyl, nitro, cyano, or sulfonamido; R 2 is hydrogen or loweralkyl; n is 1 or 2; p is --or 1; X is oxygen; and, the pharmaceutically acceptable salts thereof, wherein in said R-R 3 groups, unless otherwise stated, the loweralkyl groups contain from one to six carbon atoms; aryl and the prefix "ar" represent phenyl, naphthyl or biphenyl; the aralkyl and heteroaralkyl groups contain from one to six carbon atoms in the alkyl portion thereof and represent benzyl, phenethyl, 3,3-diphenylpropyl, or 3-indolylmethyl; heteroaryl represents indolyl, thienyl, imidazolyl, furyl, benzimidazolyl, pyridyl, quinolinyl, isoquinolinyl, and benzothienyl; aroyl denotes benzoyl or 1-naphthoyl; acylamino denotes loweralkanoylamino and aroylamino which are selected from the group consisting of acetylamino, and benzoylamino; and, alkoxy denotes a loweralkyl group bonded to oxygen.

Claim 20

The composition of claim 13 wherein said compound is a member of the group: 4-N-(1(S)-carboxyethyl)-6(R)-(1(S)-carboethoxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one; 4-N-(1(S)-carboxyethyl)-6(R)-(1(S)-carboxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one; 4-N-carboxymethyl-6(R)-(1(S)-carboethoxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one; and, 4-N-carboxymethyl-6(R)-(1(S)-carboxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one.

Claim 21

A pharmaceutical composition useful in the treatment of hypertension which comprises a pharmaceutically acceptable carrier; an antihypertensively effective amount of a compound of the formula: ##STR131## wherein: R and R 3 are independently hydrogen, C 1 -C 6 alkyl, aryl, and aralkyl; R 1 is hydrogen; hydrocarbon of from 1 to 12 carbon atoms which include branched, cyclic and straight chain hydrocarbon groups; substituted C 1 -C 6 alkyl wherein the substituent can be halo, hydroxy, carboxy, lower alkylthio, lower alkoxy, lower alkoxy carbonyl, lower aralkoxy carbonyl, amino, lower alkylamino, diloweralkylamino, or acylamino; substituted C 1 -C 6 alkyl having the formula R A (CH 2 ) n --Q--(CH 2 ) m wherein n is 0-2, m is 1-3, R A is aryl or heteroaryl optionally substituted by amino, diloweralkylamino, lower alkylamino, hydroxy, hydroxy loweralkyl, aminoloweralkyl, trihaloloweralkyl, cyano, nitro, sulfonamido, aroyl, lower alkyl, halo, dihalo, and lower alkoxy, and Q is O, S, N--R B , CONR C , NR C CO, CH═CH wherein R B is hydrogen, loweralkyl, aryl, aralkyl, lower alkanoyl, or aroyl, and R C is hydrogen or lower alkyl; aryl; substituted aryl wherein the substituent is lower alkyl, amino loweralkyl, loweralkoxy, aryloxy, aroyl, hydroxy, halo, or dihalo; aralkyl or heteroaralkyl which include branched lower alkyl groups; substituted aralkyl or substituted heteroaralkyl which include branched lower alkyl groups wherein the lower alkyl groups can be substituted by amino, acylamino, or hydroxyl and the aryl and heteroaryl groups can be substituted by halo, dihalo, loweralkyl, hydroxy, loweralkoxy, aryloxy, aroyl, arylthio, amino, amino lower alkyl, lower alkanoylamino, aroylamino, diloweralkylamino, lower alkylamino, hydroxy loweralkyl, trihalo loweralkyl, nitro, cyano, or sulfonamido; R 2 is hydrogen or loweralkyl; n is 1 or 2; p is 0 or 1; X is oxygen; or, the pharmaceutically acceptable salts thereof; wherein in said R-R 3 groups, unless otherwise stated, the loweralkyl groups contain from one to six carbon atoms; aryl and the prefix "ar" represent phenyl, naphthyl or biphenyl; the aralkyl and heteroaralkyl groups contain from one to six carbon atoms in the alkyl portion thereof and represent benzyl, phenethyl, 3,3-diphenylpropyl, or 3-indolylmethyl; heteroaryl represents indolyl, thienyl, imidazolyl, furyl, benzimidazolyl, pyridyl, quinolinyl, isoquinolinyl, and benzothienyl; aroyl denotes benzoyl or 1-naphthoyl; acylamino denotes loweralkanoylamino and aroylamino which are selected from the group consisting of acetylamino, and benzoylamino; and, alkoxy denotes a loweralkyl group bonded to oxygen, and, an antihypertensive and/or diuretic compound selected from the group consisting of hydrochlorothiazide, methyldopa, timolol, the pivaloyloxyethyl ester of methyldopa, indacrinone and variable ratios of its enantiomers, (+)-4-{3-[2-(1-hydroxycyclohexyl)ethyl]-4-oxo-2-thiazolidinyl}propyl}benzoic acid, as well as admixtures and combinations thereof.

Claim 22

A pharmaceutical composition useful in the treatment of hypertension which comprises a pharmaceutically acceptable carrier; an antihypertensively effective amount of a compound of the formula: ##STR131## wherein: R and R 3 are independently hydrogen, C 1 -C 6 alkyl, aryl, and aralkyl; R 1 is hydrogen; hydrocarbon of from 1 to 12 carbon atoms which include branched, cyclic and straight chain hydrocarbon groups; substituted C 1 -C 6 alkyl wherein the substituent can be halo, hydroxy, carboxy, lower alkylthio, lower alkoxy, lower alkoxy carbonyl, lower aralkoxy carbonyl, amino, lower alkylamino, diloweralkylamino, or acylamino; substituted C 1 -C 6 alkyl having the formula R A (CH 2 ) n --Q--(CH 2 ) m wherein n is 0-2, m is 1-3, R A is aryl or heteroaryl optionally substituted by amino, diloweralkylamino, lower alkylamino, hydroxy, hydroxy loweralkyl, aminoloweralkyl, trihaloloweralkyl, cyano, nitro, sulfonamido, aroyl, lower alkyl, halo, dihalo, and lower alkoxy, and Q is O, S, N--R B , CONR C , NR C CO, CH═CH wherein R B is hydrogen, loweralkyl, aryl, aralkyl, lower alkanoyl, or aroyl, and R C is hydrogen or lower alkyl; aryl; substituted aryl wherein the substituent is lower alkyl, amino loweralkyl, loweralkoxy, aryloxy, aroyl, hydroxy, halo, or dihalo; aralkyl or heteroaralkyl which include branched lower alkyl groups; substituted aralkyl or substituted heteroaralkyl which include branched lower alkyl groups wherein the lower alkyl groups can be substituted by amino, acylamino, or hydroxyl and the aryl and heteroaryl groups can be substituted by halo, dihalo, loweralkyl, hydroxy, loweralkoxy, aryloxy, aroyl, arylthio, amino, amino lower alkyl, lower alkanoylamino, aroylamino, diloweralkylamino, lower alkylamino, hydroxy loweralkyl, trihalo loweralkyl, nitro, cyano, or sulfonamido; R 2 is hydrogen or loweralkyl; n is 1 or 2; p is 0 or 1; X is oxygen; or, the pharmaceutically acceptable salts thereof; wherein in said R-R 3 groups, unless otherwise stated, the loweralkyl groups contain from one to six carbon atoms; aryl and the prefix "ar" represent phenyl, naphthyl or biphenyl; the aralkyl and heteroaralkyl groups contain from one to six carbon atoms in the alkyl portion thereof and represent benzyl, phenethyl, 3,3-diphenylpropyl, or 3-indolylmethyl; heteroaryl represents indolyl, thienyl, imidazolyl, furyl, benzimidazolyl, pyridyl, quinolinyl, isoquinolinyl, and benzothienyl; aroyl denotes benzoyl or 1-naphthoyl; acylamino denotes loweralkanoylamino and aroylamino which are selected from the group consisting of acetylamino, and benzoylamino; and, alkoxy denotes a loweralkyl group bonded to oxygen, and, an antihypertensive and/or diuretic compound selected from the group consisting of hydrochlorothiazide, methyldopa, timolol, the pivaloyloxyethyl ester of methyldopa, indacrinone and variable ratios of its enantiomers, (+)-4-{3-[2-(1-hydroxycyclohexyl)ethyl]-4-oxo-2-thiazolidinyl}propyl}benzoic acid, as well as admixtures and combinations thereof.

Claim 23

The composition of claim 15 wherein said pharmaceutically effective compound is a member of the group: 4-N-(1(S)-carboxyethyl)-6(R)-(1(S)-carboethoxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one; 4-N-(1(S)-carboxyethyl)-6(R)-(1(S)-carboxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one; 4-N-carboxymethyl-6(R)-(1(S)-carboethoxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one; and, 4-N-carboxymethyl-6(R)-(1(S)-carboxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one.

Claim 26

The method of claim 17 wherein said compound is a member of the group: 4-N-(1(S)-carboxyethyl)-6(R)-(1(S)-carboethoxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one; 4-N-(1(S)-carboxyethyl)-6(R)-(1(S)-carboxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one; 4-N-carboxymethyl-6(R)-(1(S)-carboethoxy-3-phenylpropylamino)perhydro- 1,4-thiazepin-5-one; and, 4-N-carboxymethyl-6(R)-(1(S)-carboxy-3-phenylpropylamino)perhydro-1,4-thiazepin-5-one.

Claim 27

A process for producing a compound having the formula: ##STR133## wherein R, R 1 , R 2 , R 3 , X, n and p are as defined in claim 1, which process comprises: reductively condensing an α-ketoacid or α-ketoester having the formula R 1 CO--CO 2 R wherein R and R 1 are as defined in claim 1 with an α-aminothialactam of the formula: ##STR134## wherein R 2 , R 3 and n are as defined in claim 1, to afford, after optionally reacting with a peracid followed by removal of protecting groups, if necessary, the desired product and, if desired, isolating the biologically more active isomer by chromatography or fractional crystallization and, if further desired, preparing a salt thereof by conventional means.

Claim 28

The process of claim 19 wherein p is 0 and n is 1.