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US4395409A Expired / Lapsed US ⏱️ 0.0 years remaining

Carbamoyloxyamino-1,4-benzodiazepines and medicaments containing these compounds

Assignee: Hoechst AG
•
Filing: 1981-06-02
•
Granted: 1983-07-26
•
Expires: 2001-06-02
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Abstract

Abstract What are disclosed are 1,4-benzodiazepines, having a carbamoyloxyamino group, of the following formula I <IMAGE> (I) tautomers thereof of the following formula IA <IMAGE> (IA) physiologically tolerated salts thereof, said compounds having an anxiolytic action without sedating, a process for the preparation of these new compounds, pharmaceutical agents which contain the active compounds, and methods for treating anxiety states with said compounds.

Inventors

  • 👤 Manfred Forsch
  • 👤 Hermann Gerhards

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 21:40
CPC Classifications
C; C07; C07D; C07D243/00; C07D243/06; C07D243/10; C07D243/14; C07D243/16; C07D243/18; C07D243/20; A; A61; A61P; A61P25/00; A61P25/26; C07D401/00; C07D401/02; C07D401/04

Claims Analysis

Total Claims: 16
Claim 1
Independent Claim 104 words
A carbamoyloxyamino-1,4-benzodiazepine of the formula ##STR12## or of the formula ##STR13## or a physiologically tolerated salt of such a compound, wherein R 1 is halogen, nitro, or trifluoromethyl; R 2 is phenyl, pyridyl, or phenyl which is mono- or di-substituted by C 1 -C 4 alkyl, C 1 -C 4 alkoxy, hydroxy, halogen, or trifluoromethyl; R 3 is hydrogen, C 1 -C 4 alkyl, monoalkylcarbamoyloxy, or dialkylcarbamoyloxy; and R 4 is phenyl or phenyl which is mono- or di-substituted by halogen, nitro, cyano, trifluoromethyl, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, hydroxy, or dialkylamino having 1-4 carbon atoms in each alkyl.
Claim 2
Dependent Claim 104 words
A carbamoyloxyamino-1,4-benzodiazepine of the formula ##STR12## or of the formula ##STR13## or a physiologically tolerated salt of such a compound, wherein R 1 is halogen, nitro, or trifluoromethyl; R 2 is phenyl, pyridyl, or phenyl which is mono- or di-substituted by C 1 -C 4 alkyl, C 1 -C 4 alkoxy, hydroxy, halogen, or trifluoromethyl; R 3 is hydrogen, C 1 -C 4 alkyl, monoalkylcarbamoyloxy, or dialkylcarbamoyloxy; and R 4 is phenyl or phenyl which is mono- or di-substituted by halogen, nitro, cyano, trifluoromethyl, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, hydroxy, or dialkylamino having 1-4 carbon atoms in each alkyl.
Claim 3
Dependent Claim 1 words
7-Chloro-2-(3-chlorophenylcarbamoyloxyamino)-5-phenyl-3H-1,4-benzodiazepine.
Claim 4
Dependent Claim 1 words
7-Chloro-2-(3-chlorophenylcarbamoyloxyamino)-5-phenyl-3H-1,4-benzodiazepine.
Claim 5
Dependent Claim 1 words
5-(2-Chlorophenyl)-2-(3-chlorophenylcarbamoyloxyamino)-7-nitro-3H-1,4-benzodiazepine.
Claim 6
Dependent Claim 1 words
5-(2-Chlorophenyl)-2-(3-chlorophenylcarbamoyloxyamino)-7-nitro-3H-1,4-benzodiazepine.
Claim 7
Dependent Claim 1 words
7-Chloro-5-(2-chlorophenyl)-2-(3-chlorophenylcarbamoyloxyamino)-3H-1,4-benzodiazepine.
Claim 8
Dependent Claim 1 words
7-Chloro-5-(2-chlorophenyl)-2-(3-chlorophenylcarbamoyloxyamino)-3H-1,4-benzodiazepine.
Claim 9
Dependent Claim 1 words
2-(3-Chlorophenylcarbamoyloxyamino)-5-(2-fluorophenyl)-7-nitro-3H-1,4-benzodiazepine.
Claim 10
Dependent Claim 1 words
2-(3-Chlorophenylcarbamoyloxyamino)-5-(2-fluorophenyl)-7-nitro-3H-1,4-benzodiazepine.
Claim 11
Dependent Claim 1 words
2-(3-Chlorophenylcarbamoyloxyamino)-7-nitro-5-phenyl-3H-1,4-benzodiazepine.
Claim 12
Dependent Claim 1 words
2-(3-Chlorophenylcarbamoyloxyamino)-7-nitro-5-phenyl-3H-1,4-benzodiazepine.
Claim 13
Dependent Claim 1 words
7-Chloro-2-(3-chlorophenylcarbamoyloxyamino)-5-(2-fluorophenyl)-3H-1,4-benzodiazepine.
Claim 14
Dependent Claim 1 words
7-Chloro-2-(3-chlorophenylcarbamoyloxyamino)-5-(2-fluorophenyl)-3H-1,4-benzodiazepine.
Claim 15
Dependent Claim 26 words
A pharmaceutical preparation for the treatment of anxiety states comprising an anxiolytic amount of a compound as in claim 1 and a pharmaceutically acceptable carrier therefor.
Claim 16
Dependent Claim 34 words
A method for treating anxiety states in a patient in need of such treatment, which method comprises orally or parenterally administering to said patient an anxiolytic amount of a compound as in claim 1.

References Cited (Backward Citations)

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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1986-07-25 1987-01-24 1987-07-26 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1990-07-25 1991-01-24 1991-07-26 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1994-07-25 1995-01-24 1995-07-26 $7700.00 Window Closed / Lapsed

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