N-Terminal substituted oligopeptide converting enzyme inhibitors

Claim 1

Compounds having the formula: ##STR44## wherein: R is hydrogen; loweralkyl; aralkyl; or, aryl; R 1 is hydrogen; alkyl of from 1 to 12 carbon atoms which include branched, cyclic and unsaturated alkyl groups; substituted loweralkyl wherein the substituent can be halo, hydroxy, carboxy, carboxamido, loweralkylthio, loweralkoxy, loweralkoxycarbonyl, loweraralkoxycarbonyl, amino, loweralkylamino, lowerdialkylamino; acylamino substituted loweralkylamino wherein the substituent can be halo, hydroxy, alkoxy or cyano; arloweralkylamino; cyclic amino; oxo, thio or ureido; aryloxy; arylthio; aralkyloxy; aralkylthio; benzofused cycloalkyl or bicycloalkyl of from 8-12 carbon atoms; aryl or heteroaryl which may be mono-, di-, or trisubstituted by loweralkyl, hydroxy, loweralkoxy, halo, amino, acylamino, lower alkylthio or aminoloweralkyl; benzofused cycloalkyl or bicycloalkyl of from 8 to 12 carbon atoms; arloweralkyl, arloweralkenyl, heteroloweralkyl and heteroloweralkenyl in which the aryl or heteroaryl rings may be mono-, di-, or trisubstituted by halo, lower alkyl, hydroxy, loweralkoxy, amino, lower alkylamino, diloweralkylamino, aminolower alkyl, acylamino, carboxy, haloloweralkyl, nitro, cyano or sulfonamido; aralkyl or heteroaralkyl which include branched loweralkyl groups; substituted aralkyl or substituted heteroaralkyl which include branched loweralkyl groups wherein the loweralkyl groups can be substituted by amino, acylamino, or hydroxyl and the aryl and heteroaryl 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, aminoloweralkyl, loweralkanoylamino, aroylamino, lowerdialkylamino, loweralkylamino, hydroxy, hydroxyloweralkyl, trihaloloweralkyl, nitro, cyano, or sulfonamido; any of the arloweralkyl or alkenyl and heteroloweralkyl or alkenyl groups described above in which the aryl or heteroaryl ring is partially or completely hydrogenated; substituted loweralkyl having the formula R A 1 (CH 2 ) n --Q--(CH 2 ) m wherein n is 0-2, m is 1-3, R A 1 is aryl or heteroaryl optionally substituted by amino, lowerdialkylamino, loweralkylamino, hydroxy, hydroxyloweralkyl, aminoloweralkyl, trihaloloweralkyl, cyano, nitro, sulfonamido, aroyl, loweralkyl, halo, dihalo, and loweralkoxy, and Q is O, S, SO, or SO 2 , N--R B 1 , CONR C 1 , NR C 1 CO, CH═CH wherein R B 1 is hydrogen, loweralkyl, aryl, aralkyl, loweralkanoyl, or aroyl, and R C 1 is hydrogen, or loweralkyl; R 2 is lower alkyl, lower alkenyl, or lower alkynyl; substituted lower alkyl, lower alkenyl or lower alkynyl in which the substituent(s) may be lower cyclo alkyl, halo, hydroxy, amino, amidino, acylamino, carboxylower alkyl amino, carbamoyllower alkylamino, hydroxy lower alkylamino, arylamino arlower alkyl amino or heteroarlower alkylamino; substituted lower alkyloxy alkyl, loweralkyl thio alkyl, and lower alkylaminoalkyl wherein the substituent(s) may be the same as those recited above; arlower alkyl and heteroarlower alkyl which may be substituted by lower alkyl, lower alkyloxy, amino, hydroxy halo or acylamino; in the group ##STR45## y is 0 to 4 A is (a) alkyl, including branched unsaturated and cyclic alkyl of 3 to 8 carbon atoms; (b) benzofused cycloalkyl or bicycloalkyl of 8 to 12 carbon atoms; (c) aryl or heteroaryl groups which may be mono-, di-, or trisubstituted by loweralkyl, loweralkoxy, halo, amino, acylamino, hydroxy, acyl or acyloxy, and corresponding groups in which the aryl or heteroaryl groups are partially or completely hydrogenated; (d) lower alkyl including branched and unsaturated groups which may be substituted by aryl or heteroaryl groups and corresponding groups in which the aryl or heteroaryl rings are partially or completely hydrogenated; B is hydrogen or loweralkyl or A and B may be joined, together with the carbon atoms to which they are attached to form a ring having the formulae: ##STR46## wherein X and Y taken together are ##STR47## wherein: R 5 and R 6 individually are hydrogen; lower alkyl; cycloalkyl; aryl; aralkyl; heteroaryl; lower alkyloxy, lower alkylthio; aryloxy; arylthio; arloweralkyloxy; arlower alkylthio; hydroxy; acyloxy; acyllower alkyl; halo; amino; mono- or disubstituted lower alkyl amino; arlower alkylamino; heteroloweralkylamino; acylamino in which the acyl group may be lower alkanoyl, aroyl, heteroaroyl or heterolower alkanoyl; carbamoyl; or N-substituted carbamoyloxy; and wherein any of these groups containing an aromatic ring, said ring may be mono-, di-, or trisubstituted by lower alkyl, lower alkoxy, loweralkylthio, halo, hydroxy, aryl, aryloxy, arylthio or aralkyl; and wherein any of said groups containing an aryl or heteroaryl group in which said groups are partially or completely hydrogenated; R 7 is hydrogen, loweralkyl, aryl, cycloalkyl, or substituted aryl wherein the substituent can be halo, hydroxy, alkoxy, amino or loweralkyl; or R 6 and R 7 taken together may be oxo, or, together with the atoms to which they are attached form a 3 to 6 membered ring which may contain 0, 1, or 2 atoms of N, S, or O; p and q are independently 0 to 3; ##STR48## wherein R 6 and R 7 are as defined above and s is 0, 1, and 2; ##STR49## wherein W is absent; --CH 2 --, ##STR50## N or S; Z is --(CH 2 ) t --, where t is 0 to 2, provided that t may not be O when W is absent; --O--; --N--, or --S--; R 8 is hydrogen; lower alkyl; loweralkoxy; hydroxy; halo, lower alkylthio; amino; acylamino; or cyano; p is 1 to 3; D is an amino acid or amino acid derivative, R 9 --R 11 , or a dipeptide R 9 --R 10 --R 11 wherein R 9 and R 10 are independently selected from alanine, leucine, isoleucine, lysine, arginine, glycine, histidine, methionine, ornithine, phenylalanine, serine, threonine, trypthophane, tyrosine, or valine, R 11 is OH, NH 2 or OR 12 wherein R 12 is loweralkyl, aryl, or aralkyl; and, the pharmaceutically acceptable salts thereof.