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US4575503A Expired / Lapsed US ⏱️ 0.0 years remaining

3-Amino-[1]-benzazepin-2-one-1-alkanoic acids

Assignee: Novartis Corp
•
Filing: 1984-02-09
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Granted: 1986-03-11
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Expires: 2004-02-09
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Abstract

Abstract Variously substituted 1-carboxymethyl-3-(carboxymethylamino)-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-ones and functional derivatives are angiotensin converting enzyme inhibitors and are useful as antihypertensive agents. Synthesis of, compositions and methods of treatment utilizing such compounds are included.

Inventors

  • 👤 Jeffrey W. H. Watthey

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 00:11
CPC Classifications
C; C07; C07K; C07K5/00; C07K5/02; C07K5/022; C07K5/0222; A; A61; A61K; A61K38/00

Claims Analysis

Total Claims: 14
Claim 1
Independent Claim 147 words
A compound of the formula ##STR25## wherein the carbocyclic ring may also be hexahydro; R 1 is indolyl(lower)alkyl, carboxy(lower)alkyl, lower alkoxycarbonyl(lower)alkyl, hydroxy(lower)alkyl, lower alkylthio(lower)alkyl, aryloxy(lower)alkyl or arylthio(lower)alkyl wherein aryl represents phenyl unsubstituted or mono- or di-substituted by lower alkyl, hydroxy, lower alkoxy, lower alkylenedioxy, lower alkanoyloxy, halogen or trifluoromethyl; R 2 and R 5 are hydrogen or lower alkyl; R 3 and R 4 are hydrogen, lower alkoxy, lower alkyl, halogen or trifluoromethyl; or R 3 and R 4 taken together on adjacent carbons represent alkylenedioxy; X represents oxo, one hydroxy or acylated hydroxy and one hydrogen, or 2 hydrogens; R 6 and R 7 independently represent hydroxy, amino, lower alkoxy, phenyl(lower)alkoxy, lower alkoxycarbonyl(lower)alkoxy; and wherein within the above definitions acylated hydroxy represents lower alkanoyloxy, nicotinoyloxy, benzoyloxy or benzoyloxy substituted on the phenyl ring by lower alkyl, halogen or lower alkoxy; or a pharmaceutically acceptable salt thereof.
Claim 2
Dependent Claim 147 words
A compound of the formula ##STR25## wherein the carbocyclic ring may also be hexahydro; R 1 is indolyl(lower)alkyl, carboxy(lower)alkyl, lower alkoxycarbonyl(lower)alkyl, hydroxy(lower)alkyl, lower alkylthio(lower)alkyl, aryloxy(lower)alkyl or arylthio(lower)alkyl wherein aryl represents phenyl unsubstituted or mono- or di-substituted by lower alkyl, hydroxy, lower alkoxy, lower alkylenedioxy, lower alkanoyloxy, halogen or trifluoromethyl; R 2 and R 5 are hydrogen or lower alkyl; R 3 and R 4 are hydrogen, lower alkoxy, lower alkyl, halogen or trifluoromethyl; or R 3 and R 4 taken together on adjacent carbons represent alkylenedioxy; X represents oxo, one hydroxy or acylated hydroxy and one hydrogen, or 2 hydrogens; R 6 and R 7 independently represent hydroxy, amino, lower alkoxy, phenyl(lower)alkoxy, lower alkoxycarbonyl(lower)alkoxy; and wherein within the above definitions acylated hydroxy represents lower alkanoyloxy, nicotinoyloxy, benzoyloxy or benzoyloxy substituted on the phenyl ring by lower alkyl, halogen or lower alkoxy; or a pharmaceutically acceptable salt thereof.
Claim 3
Dependent Claim 176 words
A compound of the formula ##STR26## wherein the carbocyclic ring may also be hexahydro; R 1 is acylamino(lower)alkyl in which acylamino represents lower alkanoylamino; lower alkoxycarbonylamino; aryl(lower)alkanoylamino; aryl(lower)alkoxycarbonylamino; or aroylamino in which aroyl represents benzoyl or benzoyl substituted by lower alkyl, lower alkoxy or halogen, or nicotinoyl; or R 1 is mono- or di(lower)alkylamino(lower)alkyl, aryl-N-(lower alkyl)-amino(lower)alkyl or arylamino(lower)alkyl wherein aryl represents phenyl unsubstituted or mono- or di substituted by lower alkyl, hydroxy, lower alkoxy, lower alkylenedioxy, lower alkanoyloxy, halogen or trifluoromethyl; R 2 and R 5 are hydrogen or lower alkyl; R 3 and R 4 are hydrogen, lower alkoxy, lower alkyl, halogen or trifluoromethyl; or R 3 and R 4 taken together represent alkylenedioxy; X represents oxo, one hydroxy or acylated hydroxy and one hydrogen, or 2 hydrogens; R 6 and R 7 independently represent hydroxy, amino, lower alkoxy, phenyl(lower)alkoxy, lower alkoxycarbonyl(lower)alkoxy; wherein the above definitions acylated hydroxy represents lower alkanoyloxy, nicotinoyloxy, benzoyloxy or benzoyloxy or benzoyloxy substituted on the phenyl ring by lower alkyl, halogen or lower alkoxy; or a pharmaceutically acceptable salt thereof.
Claim 4
Dependent Claim 176 words
A compound of the formula ##STR26## wherein the carbocyclic ring may also be hexahydro; R 1 is acylamino(lower)alkyl in which acylamino represents lower alkanoylamino; lower alkoxycarbonylamino; aryl(lower)alkanoylamino; aryl(lower)alkoxycarbonylamino; or aroylamino in which aroyl represents benzoyl or benzoyl substituted by lower alkyl, lower alkoxy or halogen, or nicotinoyl; or R 1 is mono- or di(lower)alkylamino(lower)alkyl, aryl-N-(lower alkyl)-amino(lower)alkyl or arylamino(lower)alkyl wherein aryl represents phenyl unsubstituted or mono- or di substituted by lower alkyl, hydroxy, lower alkoxy, lower alkylenedioxy, lower alkanoyloxy, halogen or trifluoromethyl; R 2 and R 5 are hydrogen or lower alkyl; R 3 and R 4 are hydrogen, lower alkoxy, lower alkyl, halogen or trifluoromethyl; or R 3 and R 4 taken together represent alkylenedioxy; X represents oxo, one hydroxy or acylated hydroxy and one hydrogen, or 2 hydrogens; R 6 and R 7 independently represent hydroxy, amino, lower alkoxy, phenyl(lower)alkoxy, lower alkoxycarbonyl(lower)alkoxy; wherein the above definitions acylated hydroxy represents lower alkanoyloxy, nicotinoyloxy, benzoyloxy or benzoyloxy or benzoyloxy substituted on the phenyl ring by lower alkyl, halogen or lower alkoxy; or a pharmaceutically acceptable salt thereof.
Claim 5
Dependent Claim 16 words
A compound according to claim 1 being 1-carboxymethyl-3-[1-ethoxycarbonyl-2-(benzylthio)ethylamino]-2,3,4,5-tetrahydro-1H-[1]-benzazepin-2-one, a stereoisomer or a pharmaceutically acceptable salt thereof.
Claim 6
Dependent Claim 16 words
A compound according to claim 1 being 1-carboxymethyl-3[1-ethoxycarbonyl-2-(3-indolyl)-ethylamino]-2,3,4,5-tetrahydro-1H[1]-benzazepin-2-one, a stereoisomer or a pharmaceutically acceptable salt thereof.
Claim 7
Dependent Claim 8 words
1-Carboxymethyl-3-[1-ethoxycarbonyl-(1S)-butyl-amino]-2,3,4,5-tetrahydro-1H-[1]-(3S)-benzazepin-2 one or a pharmaceutically acceptable salt thereof.
Claim 8
Dependent Claim 8 words
1-Carboxymethyl-3-[1-ethoxycarbonyl-(1S)-butyl-amino]-2,3,4,5-tetrahydro-1H-[1]-(3S)-benzazepin-2 one or a pharmaceutically acceptable salt thereof.
Claim 9
Dependent Claim 16 words
A compound according to claim 1 being 1-carboxymethyl-3-[1-ethoxycarbonyl-3-methylthiopropylamino]-2,3,4,5-tetrahydro-1H-[1]-benzazepin-2-one, a stereoisomer or a pharmaceutically acceptable salt thereof.
Claim 10
Dependent Claim 17 words
A compound according to claim 1 being 1-carboxymethyl-3-[1-ethoxycarbonyl-2-benzyloxyethylamino]-2,3,4,5-tetrahydro-1H-[1]-benzazepin-2 one, a stereoisomer or a pharmaceutically acceptable salt thereof.
Claim 11
Dependent Claim 16 words
A compound according to claim 2 being 1-carboxymethyl-3-[1-ethoxycarbonyl-5-(benzoylamino)-pentylamino]-2,3,4,5-tetrahydro-1H-[1]-benzazepin-2-one, a stereoisomer or a pharmaceutically acceptable salt thereof.
Claim 12
Dependent Claim 43 words
A pharmaceutical composition suitable for oral or parenteral administration to mammals for the treatment or prevention of diseases responsive to inhibition of angiotensin-converting enzyme comprising an effective amount of a compound of claim 1 in combination with one or more pharmaceutically acceptable carriers.
Claim 13
Dependent Claim 28 words
A method of treating hypertensive or cardiac conditions in mammals which comprises administering to a mammal in need thereof an effective amount of a composition of claim 9.
Claim 14
Dependent Claim 24 words
A method of inhibiting angiotensin-converting enzyme which comprises administering to a mammal in need thereof an effective amount of a composition of claim 9.

References Cited (Backward Citations)

GB2103614A Cited
EP0072352B1 Cited
US4410520A Cited
ZA829141B Cited
ZA833903B Cited
US4473575A Cited
EP0107095A1 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1989-03-10 1989-09-09 1990-03-11 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1993-03-10 1993-09-09 1994-03-11 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1997-03-10 1997-09-09 1998-03-11 $7700.00 Window Closed / Lapsed

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