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Substituted phenylpiperazine derivatives

Assignee: Hoechst AG
•
Filing: 1979-06-04
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Granted: 1980-11-18
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Expires: 1999-06-04
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Abstract

Abstract Phenylpiperazine derivatives of the formula I ##STR1## in which R 1 denotes hydrogen or C 1 -C 6 alkyl, R 2 denotes hydrogen or one or several, identical or different substituents selected from the group of C 1 -C 6 -alkyl, C 1 -C 6 alkoxy, halogen, trifluoromethyl, hydroxy, nitro, amino and methylene-dioxy, R 3 denotes hydrogen, hydroxy, C 1 -C 6 alkanoyloxy, and n is 1 or 2, and the physiologically acceptable salts thereof, processes for their manufacture and medicaments containing or consisting of said compounds.

Inventors

  • 👤 Rudolf Lattrell
  • 👤 Wilhelm Bartmann
  • 👤 Hermann Gerhards

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-28 13:46
CPC Classifications
C; C07; C07D; C07D209/00; C07D209/02; C07D209/04; C07D209/08; C07D209/30; C07D209/32; C07D209/34; C07D215/00; C07D215/02; C07D215/16; C07D215/38

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 73 words
A phenylpiperazine compound of the formula ##STR25## or a physiologically acceptable salt thereof, wherein R 1 denotes hydrogen or C 1 -C 6 alkyl, R 2 denotes one or several, identical or different, members selected from the group consisting of C 1 -C 6 -alkyl, C 1 -C 6 alkoxy, halogen, trifluoromethyl, hydroxy, nitro, amino, and methylene-dioxy, R 3 denotes hydrogen, hydroxy, C 1 -C 6 alkanoyloxy, and n is 1 or 2.
Claim 2
Dependent Claim 73 words
A phenylpiperazine compound of the formula ##STR25## or a physiologically acceptable salt thereof, wherein R 1 denotes hydrogen or C 1 -C 6 alkyl, R 2 denotes one or several, identical or different, members selected from the group consisting of C 1 -C 6 -alkyl, C 1 -C 6 alkoxy, halogen, trifluoromethyl, hydroxy, nitro, amino, and methylene-dioxy, R 3 denotes hydrogen, hydroxy, C 1 -C 6 alkanoyloxy, and n is 1 or 2.
Claim 3
Dependent Claim 20 words
A neuroleptic composition comprising a compound as defined in claim 1 and a physiologically acceptable auxiliary agent or carrier therefor.
Claim 4
Dependent Claim 36 words
The method of treating a human patient to produce a neuroleptic effect which comprises orally administering to said patient of a dose of about 20 to 800 mg/day of a compound as defined in claim 1.
Claim 5
Dependent Claim 35 words
The method of treating a human patient to produce a neuroleptic effect which comprises intravenously administering to said patient a dose of about 5 to 300 mg/day of a compound as defined in claim 1.

References Cited (Backward Citations)

US3910924A Cited
US3929793A Cited
US4147869A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-11-18 1984-05-19 1984-11-18 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-11-18 1988-05-19 1988-11-18 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-11-18 1992-05-19 1992-11-18 $7700.00 Window Closed / Lapsed

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