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US4029790A Expired / Lapsed US ⏱️ 0.0 years remaining

1-Benzoyl-2 or 4 [2-(4-phenyl-piperazino)-ethyl]-piperidines

Assignee: Centre Europeen de Recherches Mauvernay CERM
•
Filing: 1975-09-26
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Granted: 1977-06-14
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Expires: 1995-09-26
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Abstract

Abstract Compounds of the formula ##STR1## and pharmaceutically acceptable acid salts thereof, wherein X is hydrogen, halogen or methoxy, n is zero, Y is halogen and the ethyl piperazaine moiety is attached to the 2- or 4- position of the piperidine ring, is described. These compounds have anti-spasmolytic and antitussive activity.

Inventors

  • 👤 Roland Yves Mauvernay
  • 👤 Norbert Busch
  • 👤 Jacques Moleyre
  • 👤 Jacques Simond
  • 👤 Andre Monteil

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 18:08
CPC Classifications
C; C07; C07D; C07D401/00; C07D401/02; C07D401/06

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 50 words
A compound of the formula: ##STR5## and salts thereof with pharmaceutically acceptable acids in which X represents a hydrogen or halogen atom or methoxy group, n is 0; Y represents a halogen atom; and the ethyl piperazine moiety is attached to the 2- or 4- position of the piperidine ring.
Claim 2
Dependent Claim 50 words
A compound of the formula: ##STR5## and salts thereof with pharmaceutically acceptable acids in which X represents a hydrogen or halogen atom or methoxy group, n is 0; Y represents a halogen atom; and the ethyl piperazine moiety is attached to the 2- or 4- position of the piperidine ring.
Claim 3
Dependent Claim 4 words
1-Benzoyl 2-{2-[4-(4-fluoro)phenyl)piperazinyl} ethyl piperidine.
Claim 4
Dependent Claim 4 words
1-Benzoyl 2-{2-[4-(4-fluoro)phenyl)piperazinyl} ethyl piperidine.
Claim 5
Dependent Claim 5 words
1-(4-Chloro)benzoyl 2-{(2-[4-(4-fluoro)phenyl] piperazinyl} ethyl piperidine.
Claim 6
Dependent Claim 5 words
1-(4-Chloro)benzoyl 2-{(2-[4-(4-fluoro)phenyl] piperazinyl} ethyl piperidine.
Claim 7
Dependent Claim 3 words
1-(4-Fluoro)benzoyl 2-{2-[4-(4-fluoro)phenyl]piperazinyl}ethyl piperidine.
Claim 8
Dependent Claim 3 words
1-(4-Fluoro)benzoyl 2-{2-[4-(4-fluoro)phenyl]piperazinyl}ethyl piperidine.
Claim 9
Dependent Claim 4 words
1-(4-Chloro)benzoyl 4-{2-[ 4-(4-chloro)phenyl]piperazinyl}ethyl piperidine.
Claim 10
Dependent Claim 4 words
1-(4-Chloro)benzoyl 4-{2-[ 4-(4-chloro)phenyl]piperazinyl}ethyl piperidine.
Claim 11
Dependent Claim 5 words
1-(4-Chloro)benzoyl 4-{ 2-[4-(4-fluoro)phenyl]piperazinyl} ethyl piperidine.
Claim 12
Dependent Claim 5 words
1-(4-Chloro)benzoyl 4-{ 2-[4-(4-fluoro)phenyl]piperazinyl} ethyl piperidine.
Claim 13
Dependent Claim 6 words
1-(-Fluoro)benzoyl 4-{ 2[ 4-[ 4-fluoro)phenyl]piperzinyl}ethyl piperidine.
Claim 14
Dependent Claim 6 words
1-(-Fluoro)benzoyl 4-{ 2[ 4-[ 4-fluoro)phenyl]piperzinyl}ethyl piperidine.
Claim 15
Dependent Claim 65 words
A pharmaceutical composition consisting essentially of a compound of ##STR6## and salts thereof with pharmaceutically acceptable acids in which X represents a hydrogen or halogen atom or a lower alkoxy group, n is 0; Y represents a halogen atom; and the ethyl piperazine moiety is attached to the 2- or 4- position of the piperidine ring in association with a pharmaceutically acceptable carrier or diluent.
Claim 16
Dependent Claim 65 words
A pharmaceutical composition consisting essentially of a compound of ##STR6## and salts thereof with pharmaceutically acceptable acids in which X represents a hydrogen or halogen atom or a lower alkoxy group, n is 0; Y represents a halogen atom; and the ethyl piperazine moiety is attached to the 2- or 4- position of the piperidine ring in association with a pharmaceutically acceptable carrier or diluent.
Claim 17
Independent Claim 71 words
A method of treating bronchospasmolytic and tussive conditions by administering a formula: ##STR7## or pharmaceutically acceptable acid salts thereof in which X represents a hydrogen or halogen atom or methoxy group, n is 0; Y represents a halogen atom; and the ethyl piperazine moiety is attached to the 2- or 4- position of the piperidine ring in dosages of from 10 to 500 mg per day in an orally acceptable form.
Claim 18
Independent Claim 71 words
A method of treating bronchospasmolytic and tussive conditions by administering a formula: ##STR7## or pharmaceutically acceptable acid salts thereof in which X represents a hydrogen or halogen atom or methoxy group, n is 0; Y represents a halogen atom; and the ethyl piperazine moiety is attached to the 2- or 4- position of the piperidine ring in dosages of from 10 to 500 mg per day in an orally acceptable form.

References Cited (Backward Citations)

US3729474A Cited
US3753985A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1980-06-13 1980-12-13 1981-06-14 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-06-13 1984-12-13 1985-06-14 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-06-13 1988-12-13 1989-06-14 $7700.00 Window Closed / Lapsed

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