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US5075302A Expired / Lapsed US ⏱️ 0.0 years remaining

Mercaptoacyl aminolactam endopeptidase inhibitors

Assignee: Merck Sharp & Dohme LLC
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Filing: 1990-03-09
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Granted: 1991-12-24
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Expires: 2010-03-09
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Abstract

Abstract Mercaptoacyl aminolactam inhibitors of endopeptidases of the formula <IMAGE> wherein Y is -(CHR5)n(CR3R4)- or -(CR3R4)pX(CR3R4)q-, wherein two substituents selected from the group consisting of R3, R4 and R5, can form a benzene, cyclopentane or cyclohexane ring; X is -O-, -S-, -SO- or -SO2-; Q is hydrogen or R6CO-; m is 1 or 2; n is 1, 2, 3 or 4; p is 1 or 2; q is 2 or 3; R1 is lower alkyl, aryl or heteroaryl; R2 is hydrogen, lower alkyl, hydroxylower alkyl, lower alkoxylower alkyl, aryllower alkyl or heteroaryllower alkyl; R3 and R4 are independently hydrogen, lower alkyl, aryllower alkyl or heteroaryllower alkyl; R5 is hydrogen, lower alkyl, aryllower alkyl, heteroaryllower alkyl, hydroxy, lower alkoxy, mercapto, or lower alkylthio; and R6 is lower alkyl, aryl or heteroaryl, use of the compounds, alone or in combination with an ACE inhibitor or an ANF, in the treatment of cardiovascular disorders such as hypertension, congestive heart failure, edema and renal insufficiency, use of the compounds in the treatment of pain conditions, and pharmaceutical compositions containing said compounds are disclosed.

Inventors

  • 👤 Bernard R. Neustadt

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 02:35
CPC Classifications
C; C07; C07D; C07D211/00; C07D211/04; C07D211/68; C07D211/72; C07D211/74; C07D211/76; A; A61; A61P; A61P13/00; A61P13/02; A61P15/00; A61P3/00; A61P43/00; A61P9/00; A61P9/12; C07D223/00; C07D223/02; C07D223/06; C07D223/12

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 325 words
A compound represented by the formula ##STR49## wherein Y is -(CHR 5 ) n -(CR 3 R 4 )- or -(CR 3 R 4 ) p X(CR 3 R 4 ) q -, wherein two substituents selected from the group consisting of R 3 , R 4 and R 5 , together with the carbons to which the substituents are attached, when the substituents are present on adjacent carbon atoms, can form a benzene, cyclopentane or cyclohexane ring; X is -O-, -S-, -SO- or -SO 2 -; Q is hydrogen or R 6 CO-; m is 1 or 2; n is 1, 2, 3 or 4; p is 1 or 2; q is 2 or 3; R 1 is lower alkyl; aryl, selected from the group consisting of phenyl, naphthyl, substituted phenyl and substituted naphthyl, wherein said substituted phenyl and substituted naphthyl groups are substituted with 1-3 substituents selected from the group consisting of lower alkyl, hydroxy, lower alkoxy, halo, trifluoromethyl, phenyl, phenoxy and phenylthio; heteroaryl or substituted heteroaryl, wherein heteroaryl is selected from the group consisting of furanyl, thienyl, pyrrolyl and pyridyl, and wherein said substituted heteroaryl is substituted with 1-3 substituents selected from the group consisting of lower alkyl, hydroxy, lower alkoxy, halo, trifluoromethyl, phenyl, phenoxy and phenylthio; R 2 is hydrogen, lower alkyl, hydroxylower alkyl, loweralkoxylower alkyl, aryllower alkyl, heteroaryllower alkyl, substituted-aryllower alkyl, or substituted-heteroaryllower alkyl, wherein aryl, heteroaryl, substituted aryl and substituted heteraryl are as defined above; R 3 and R 4 are independently hydrogen, lower alkyl, aryllower alkyl, heteroaryllower alkyl, substituted-aryllower alkyl, or substituted-heteroaryllower alkyl, wherein aryl, heteroaryl, substituted aryl and substituted heteroaryl are as defined above; R 5 is hydrogen, lower alkyl, aryllower alkyl, heteroaryllower alkyl, hydroxy, lower alkoxy, mercapto, lower alkylthio, substituted-aryllower alkyl, or substituted-heteroaryllower alkyl, wherein aryl, heteroaryl, substituted aryl and substituted heteroaryl are as defined above; and R 6 is lower alkyl, aryl, heteroaryl, wherein aryl, heteroaryl, substituted aryl and substituted heteroaryl are as defined above.
Claim 2
Dependent Claim 325 words
A compound represented by the formula ##STR49## wherein Y is -(CHR 5 ) n -(CR 3 R 4 )- or -(CR 3 R 4 ) p X(CR 3 R 4 ) q -, wherein two substituents selected from the group consisting of R 3 , R 4 and R 5 , together with the carbons to which the substituents are attached, when the substituents are present on adjacent carbon atoms, can form a benzene, cyclopentane or cyclohexane ring; X is -O-, -S-, -SO- or -SO 2 -; Q is hydrogen or R 6 CO-; m is 1 or 2; n is 1, 2, 3 or 4; p is 1 or 2; q is 2 or 3; R 1 is lower alkyl; aryl, selected from the group consisting of phenyl, naphthyl, substituted phenyl and substituted naphthyl, wherein said substituted phenyl and substituted naphthyl groups are substituted with 1-3 substituents selected from the group consisting of lower alkyl, hydroxy, lower alkoxy, halo, trifluoromethyl, phenyl, phenoxy and phenylthio; heteroaryl or substituted heteroaryl, wherein heteroaryl is selected from the group consisting of furanyl, thienyl, pyrrolyl and pyridyl, and wherein said substituted heteroaryl is substituted with 1-3 substituents selected from the group consisting of lower alkyl, hydroxy, lower alkoxy, halo, trifluoromethyl, phenyl, phenoxy and phenylthio; R 2 is hydrogen, lower alkyl, hydroxylower alkyl, loweralkoxylower alkyl, aryllower alkyl, heteroaryllower alkyl, substituted-aryllower alkyl, or substituted-heteroaryllower alkyl, wherein aryl, heteroaryl, substituted aryl and substituted heteraryl are as defined above; R 3 and R 4 are independently hydrogen, lower alkyl, aryllower alkyl, heteroaryllower alkyl, substituted-aryllower alkyl, or substituted-heteroaryllower alkyl, wherein aryl, heteroaryl, substituted aryl and substituted heteroaryl are as defined above; R 5 is hydrogen, lower alkyl, aryllower alkyl, heteroaryllower alkyl, hydroxy, lower alkoxy, mercapto, lower alkylthio, substituted-aryllower alkyl, or substituted-heteroaryllower alkyl, wherein aryl, heteroaryl, substituted aryl and substituted heteroaryl are as defined above; and R 6 is lower alkyl, aryl, heteroaryl, wherein aryl, heteroaryl, substituted aryl and substituted heteroaryl are as defined above.
Claim 3
Dependent Claim 17 words
A compound of claim 1 wherein Y is -(CHR 5 ) n (CR 3 R 4 )-.
Claim 4
Dependent Claim 17 words
A compound of claim 2 wherein R 3 , R 4 and R 5 are each hydrogen.
Claim 5
Dependent Claim 11 words
A compound of claim 3 wherein n is 2 or 3.
Claim 6
Dependent Claim 10 words
A compound of claim 1 wherein R 2 is hydrogen.
Claim 7
Dependent Claim 17 words
A compound of claim 1 wherein R 1 is phenyl or lower alkylphenyl and m is 1.
Claim 8
Dependent Claim 11 words
A compound of claim 1 wherein Q is hydrogen or acetyl.
Claim 9
Dependent Claim 12 words
A compound of claim 1 which is: 3(S)-[2-acetylthiomethyl-3-phenylpropionyl]amino-ε-caprolactam; 3(S)-[2(S)-acetylthiomethyl-3-(2-methylphenyl)propionyl]amino-ε-caprolactam; 3(S)-[2(S)-mercaptomethyl-3-(2-methylphenyl)propionyl]amino-ε-caprolactam; 3(S)-[2(S)-acetylthiomethyl-3-(2-methylphenyl)propionyl]amino-δ-valerolactam; 3(S)-[2(S)-mercaptomethyl-3-(2-methylphenyl)propionyl]amino-δ-valerolactam.
Claim 10
Dependent Claim 30 words
A method for treating hypertension or congestive heart failure in mammals comprising administering to a mammal in need of such treatment an effective amount of a compound of claim 1.
Claim 11
Dependent Claim 18 words
A pharmaceutical composition comprising an effective amount of a compound of claim 1 in a pharmaceutically acceptable carrier.

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Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1994-12-23 1995-06-24 1995-12-24 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1998-12-23 1999-06-24 1999-12-24 $3760.00 Window Closed / Lapsed
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