Details for Patent: 5,659,065

Title:	Alpha-aminoalkanoic acids and reduction products
Abstract:	Compounds of formula I ##STR1## wherein R.sub.1 is an aliphatic, cycloaliphatic, cycloaliphatic-aliphatic, aromatic or heteroaromatic radical, a hydroxy group that is aliphatically, araliphatically or heteroarylaliphatically etherified or protected by a hydroxy-protecting group, or an aliphatically etherified mercapto group, and R.sub.2 is an aliphatic, cycloaliphatic, cycloaliphatic-aliphatic, araliphatic or heteroarylaliphatic radical, or R.sub.1 and R.sub.2 together form a divalent aliphatic radical, R.sub.3 is free or aliphatically, araliphatically or aromatically esterified carboxy, formyl or hydroxymethyl, R.sub.4 is hydrogen, an aliphatic or araliphatic radical or an amino-protecting group, and R.sub.5 is hydrogen or an aliphatic radical, and the salts thereof can be used as intermediates in the preparation of medicinal active ingredients.
Inventor(s):	Goschke; Richard (Bottmingen, CH)
Assignee:	Novartis Corporation (Tarrytown, NY)
Filing Date:	Apr 04, 1995
Application Number:	08/416,240
Claims:	1. A compound of formula Ib ##STR27## wherein R.sub.2 is lower alkyl, 3- to 8-membered cycloalkyl, 3- to 8-membered cycloalkyl-lower alkyl, or a lower alkyl radical that is unsubstituted or substituted in the phenyl, naphthyl or heteroaryl moiety by lower alkyl, lower alkoxy, halogen and/or by trifluoromethyl, R.sub.3 is formyl, hydroxymethyl, carboxy, lower alkoxycarbonyl, lower alkenyloxycarbonyl or an unsubstituted or lower alkyl-, lower alkoxy-, halo- and/or trifluoromethyl-substituted phenyl-lower alkoxycarbonyl or phenyloxycarbonyl radical, R.sub.4 is hydrogen, lower alkyl, an unsubstituted or lower alkyl-, lower alkoxy, halo- and/or trifluoromethyl-substituted phenyl- or naphthyl-lower alkyl radical, lower alkanoyl, tri-halo-lower alkanoyl, an unsubstituted or lower alkyl-, lower alkoxy-, halo-, trifluoromethyl- and/or nitro-substituted benzoyl or phenyl-lower alkoxycarbonyl group, tri-lower alkylsilyl or benzyl-(di-lower alkyl)silyl, R.sub.5 is hydrogen or lower alkyl, R.sub.6 is hydrogen, hydroxy, lower alkoxy, cycloalkoxy, lower alkoxy-lower alkoxy, carboxy-lower alkoxy, lower alkoxycarbonyl-lower alkoxy, carbamoyl-lower alkoxy or N-mono- or N,N-di-lower alkylcarbamoyl-lower alkoxy, R.sub.7 is hydrogen, lower alkyl, cycloalkyl, lower alkoxy-lower alkyl, lower alkoxy-lower alkoxy-lower alkyl, cycloalkoxy-lower alkyl, hydroxy, lower alkanoyloxy-lower alkyl, hydroxy-lower alkoxy, halo-(hydroxy)-lower alkoxy, lower alkanesulfonyl-(hydroxy)-lower alkoxy, amino-lower alkyl, lower alkylamino-lower alkyl, di-lower alkylamino-lower alkyl, lower alkanoylamino-lower alkyl, lower alkoxycarbonylamino-lower alkyl, lower alkoxyimino-lower alkyl, amino-lower alkoxy, lower alkylamino-lower alkoxy, di-lower alkylamino-lower alkoxy, lower alkanoylamino-lower alkoxy, lower alkoxycarbonylamino-lower alkoxy, oxo-lower alkoxy, lower alkoxy, cycloalkoxy, lower alkenyloxy, cycloalkoxy-lower alkoxy, lower alkoxy-lower alkoxy, lower alkoxy-lower alkenyl, lower alkenyloxy-lower alkoxy, lower alkoxy-lower alkenyloxy, lower alkenyloxy-lower alkyl, lower alkanoyl-lower alkoxy, lower alkylthio-lower alkoxy, lower alkanesulfonyl-lower alkoxy, lower alkylthio-(hydroxy)-lower alkoxy, aryl-lower alkoxy, thiazolylthio-lower alkoxy or thiazolinylthio-lower alkoxy, imidazolylthio-lower alkoxy, optionally N-oxidised pyridylthio-lower alkoxy, pyrimidinylthio-lower alkoxy, cyano-lower alkoxy, lower alkoxycarbonyl-lower alkoxy, carbamoyl-lower alkoxy, N-mono- or N,N-di-lower alkylcarbamoyl-lower alkoxy, carboxy-lower alkyl, lower alkoxycarbonyl-lower alkyl, carbamoyl-lower alkyl or N-mono- or N,N-di-lower alkylcarbamoyl-lower alkyl, R.sub.8 is lower alkyl, polyhalo-lower alkyl, lower alkoxy-lower alkyl, cycloalkoxy-lower alkyl, hydroxy-lower alkyl, lower alkylthio-lower alkyl, lower alkanesulfonyl-lower alkyl, optionally partially hydrogenated or N-oxidised pyridyl-lower alkyl, thiazolylthio-lower alkyl or thiazolinylthio-lower alkyl, imidazolylthio-lower alkyl, optionally N-oxidised pyridylthio-lower alkyl, pyrimidinylthio-lower alkyl, amino-lower alkyl, lower alkylamino-lower alkyl, di-lower alkylamino-lower alkyl, lower alkanoylamino-lower alkyl, lower alkanesulfonylamino-lower alkyl, polyhalo-lower alkanesulfonylamino-lower alkyl, pyrrolidino-lower alkyl, piperidino-lower alkyl, piperazino-, N'-lower alkylpiperazino- or N'-lower alkanoylpiperazino-lower alkyl, morpholino-lower alkyl, thiomorpholino-, S-oxothiomorpholino- or S,S-dioxothiomorpholino-lower alkyl, cyano-lower alkoxy, carboxy-lower alkyl, lower alkoxycarbonyl-lower alkyl, carbamoyl-lower alkyl, N-mono- or N,N-di-lower alkylcarbamoyl-lower alkyl, cycloalkyl; phenyl or naphthyl that is unsubstituted or mono-, di- or tri-substituted by lower alkyl, lower alkoxy, hydroxy, lower alkylamino, di-lower alkylamino, halogen and/or by trifluoromethyl; hydroxy, lower alkoxy, cycloalkoxy, lower alkoxy-lower alkoxy, cycloalkoxy-lower alkoxy, hydroxy-lower alkoxy; phenyl-lower alkoxy or naphthyl-lower alkoxy that is unsubstituted or mono-, di- or tri-substituted by lower alkyl, lower alkoxy, hydroxy, lower alkylamino, di-lower alkylamino, halogen and/or by trifluoromethyl; lower alkoxy, polyhalo-lower alkoxy, lower alkylthio-lower alkoxy, lower alkanesulfonyl-lower alkoxy, optionally hydrogenated heteroaryl-lower alkoxy, optionally partially or fully hydrogenated heteroarylthio-lower alkoxy, such as thiazolylthio-lower alkoxy or thiazolinylthio-lower alkoxy, imidazolylthio-lower alkoxy, optionally N-oxidised pyridylthio-lower alkoxy, pyrimidinylthio-lower alkoxy, amino-lower alkoxy, lower alkylamino-lower alkoxy, di-lower alkylamino-lower alkoxy, lower alkanoylamino-lower alkoxy, lower alkanesulfonylamino-lower alkoxy, polyhalo-lower alkanesulfonylamino-lower alkoxy, pyrrolidino-lower alkoxy, piperidino-lower alkoxy, piperazino-, N'-lower alkylpiperazino- or N'-lower alkanoylpiperazino-lower alkoxy, morpholino-lower alkoxy, thiomorpholino-, S-oxothiomorpholino- or S,S-dioxothiomorpholino-lower alkoxy, cyano-lower alkoxy, carboxy-lower alkoxy, lower alkoxycarbonyl-lower alkoxy, carbamoyl-lower alkoxy or N-mono-, or N,N-di-lower alkylcarbamoyl-lower alkoxy, or together with R.sub.9 is lower alkylenedioxyl or a fused-on benzo or cyclohexeno ring, R.sub.9 together with R.sub.8 is lower alkylenedioxy or a fused-on benzo or cyclohexeno ring, or is hydrogen, lower alkyl, hydroxy, lower alkoxy or cycloalkoxy, or a salt thereof. 2. A compound according to claim 1 of formula Ib wherein R.sub.2 is lower alkyl, 3- to 5-membered cycloalkyl-lower alkyl or cycloalkyl, R.sub.3 is carboxy, lower alkoxycarbonyl, formyl or hydroxymethyl, R.sub.4 is lower alkoxycarbonyl or unsubstituted or lower alkyl-, lower alkoxy-, nitro- and/or halo-substituted .alpha.-phenyl-lower alkoxycarbonyl, R.sub.5 and R.sub.6 are hydrogen, R.sub.7 is lower alkyl, lower alkoxy-lower alkyl, lower alkoxy-lower alkoxy, lower alkoxy-lower alkoxy-lower alkyl, unsubstituted or lower alkyl-, lower alkoxy-, hydroxy-, halo-, nitro- and/or amino-substituted phenyl-lower alkoxy, optionally N-oxidised pyridyl-lower alkoxy, lower alkylthio-lower alkoxy, lower alkanesulfonyl-lower alkoxy, lower alkanoyl-lower alkoxy, optionally N-oxidised pyridyl-lower alkoxy, cyano-lower alkoxy, carboxy-lower alkoxy, lower alkoxycarbonyl-lower alkoxy, carbamoyl-lower alkoxy, lower alkylcarbamoyl-lower alkoxy or di-lower alkylcarbamoyl-lower alkoxy, R.sub.8 is hydrogen, lower alkyl, hydroxy, lower alkoxy or polyhalo-lower alkoxy or together with R.sub.9 is lower alkylenedioxy, and R.sub.9 is hydrogen or together with R.sub.8 is lower alkylenedioxy, or a salt thereof. 3. A compound according to claim 1 of formula Ib wherein R.sub.2 is branched C.sub.1 -C.sub.4 alkyl or 3- to 5-membered cycloalkyl-C.sub.1 -C.sub.4 alkyl, R.sub.3 is carboxy, C.sub.1 -C.sub.4 alkoxycarbonyl, formyl or hydroxymethyl, R.sub.4 is C.sub.1 -C.sub.4 alkoxycarbonyl or .alpha.-phenyl-C.sub.1 -C.sub.4 alkoxycarbonyl, R.sub.5 and R.sub.6 are hydrogen, R.sub.7 is C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy-C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy-C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkoxy-C.sub.1 -C.sub.4 alkoxy-C.sub.1 -C.sub.4 alkyl, phenyl-C.sub.1 -C.sub.4 alkoxy, pyridyl-C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkylthio-C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkanesulfonyl-C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkanoyl-C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkoxycarbonyl-C.sub.1 -C.sub.4 alkoxy, carbamoyl-C.sub.1 -C.sub.4 alkoxy or di-C.sub.1 -C.sub.4 alkylcarbamoyl-C.sub.1 -C.sub.4 alkoxy, R.sub.8 is hydrogen, C.sub.1 -C.sub.4 alkyl, hydroxy or C.sub.1 -C.sub.4 alkoxy or together with R.sub.9 is C.sub.1 -C.sub.4 alkylenedioxyl, and R.sub.9 is hydrogen or together with R.sub.8 is C.sub.1 -C.sub.4 alkylenedioxy, or a salt thereof. 4. A compound according to claim 1 of formula Ib wherein R.sub.2 is branched C.sub.1 -C.sub.4 alkyl, R.sub.3 is carboxy, formyl or hydroxymethyl, R.sub.4 is C.sub.1 -C.sub.4 alkoxycarbonyl, R.sub.5, R.sub.6 and R.sub.9 are hydrogen, R.sub.7 is C.sub.1 -C.sub.4 alkoxy-C.sub.1 -C.sub.4 alkoxy or C.sub.1 -C.sub.4 alkoxy-C.sub.1 -C.sub.4 alkyl, and R.sub.8 is hydrogen, C.sub.1 -C.sub.4 alkyl or C.sub.1 -C.sub.4 alkoxy, or a salt thereof. 5. A compound as claimed in claim 1 being 2(S)-Amino-4(S)-[4-methoxy-3-(3-methoxypropoxy)-benzyl]-5-methyl-hexanoic acid ethyl ester, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-[4-methoxy-3-(3-methoxypropoxy)-benzyl ]-5-methyl-hexanoic acid ethyl ester, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-(p-tert-butylphenyl)-5-methyl-hexanoic acid ethyl ester, 2(S)-(Tert-butoxycarbonyl)amino-4(R)-(p-tert-butylbenzyl)-hexanoic acid ethyl ester, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-[4tert-butyl-3-(3-methoxypropoxy)-benz yl]-5-ethyl-hexanoic acid ethyl ester, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-[3-benzyloxy-4,5-ethylenedioxy-benzyl] -5-methyl-hexanoic acid ethyl ester, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-[4-ethyl-3-(3-methoxypropoxy)-benzyl]- 5-methyl-hexanoic acid ethyl ester, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-[3-benzyloxy-4-methoxy-benzyl]-5-methy l-hexanoic acid ethyl ester, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-[4-benzyloxy-3-(3-methoxy-propoxy)-ben zyl]-5-methyl-hexanoic acid ethyl ester, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-benzyloxymethyl-5-methyl-hexanoic acid ethyl ester, 2(S) -(Tert-butoxycarbonyl)amino-4(S)-[4-methoxy-3-(3-methoxypropoxy)-benzyl]-5 -methyl-hexan-1-ol, 2(S)-Tert-butoxycarbonyl)amino-4(S)-[4-methoxy-3-(3-methoxypropoxy)-benzyl] -5-methyl-hexanal, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-(p-tert-butyl-benzyl)-5-methyl-hexanal 2(S)-(Tert-butoxycarbonyl)amino-4(R)-(p-tert-butyl-benzyl)-hexanal, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-[4-tert-butyl-3-(3-methoxypropoxy)-ben zyl]-5-methyl-hexanal, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-[3-benzyloxy-4,5-ethylenedioxy-benzyl] -5-methyl-hexanal, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-[4-ethyl-3-(3-methoxypropoxy)-benzyl]- 5-methyl-hexanal, 2(S)-(Tert-butoxycarbonyl)amino-4(S)-[4-methoxy-3-benzyloxy-benzyl]-5-methy l-hexanal, or 2(S)-(Tert-butoxycarbonyl)amino-4(S)-[4-benzyloxy-3-(3-methoxy-propoxy)-ben zyl]-5-methyl-hexanal, or a salt thereof.