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N-aralkyl piperidine methanol derivatives and the uses thereof

Assignee: Aventis Pharmaceuticals Inc
•
Filing: 1987-07-07
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Granted: 1988-11-08
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Expires: 2007-07-07
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Abstract

Abstract This invention relates to a new class of compounds having important biochemical and pharmacological properties. More particularly, this invention relates to N-aralkyl piperidinemethanol derivatives which are potent and selective inhibitors of the binding of serotonin at the 5HT 2 receptor site, and to the processes for their preparation and use.

Inventors

  • 👤 Albert A. Carr
  • 👤 Norbert L. Wiech

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 13:57
CPC Classifications
C; C07; C07D; C07D211/00; C07D211/04; C07D211/06; C07D211/08; C07D211/18; C07D211/20; C07D211/22

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 86 words
A method for the treatment of cardiac arrhythmias comprising administering to a patient in need thereof, by an enteral or a parenteral route of administration, an antiarrhythmic amount of a compound of the formula: ##STR3## the optical isomers thereof, and the pharamaceutically acceptable salts thereof, wherein n is 2, 3, or 4, each of R 1 , R 2 , R 3 , and R 4 is independently selected from the group consisting of hydrogen, halogen, trifluoromethyl, C 1-6 alkyl, C 1-6 alkoxy, hydroxy and amino.
Claim 2
Independent Claim 86 words
A method for the treatment of cardiac arrhythmias comprising administering to a patient in need thereof, by an enteral or a parenteral route of administration, an antiarrhythmic amount of a compound of the formula: ##STR3## the optical isomers thereof, and the pharamaceutically acceptable salts thereof, wherein n is 2, 3, or 4, each of R 1 , R 2 , R 3 , and R 4 is independently selected from the group consisting of hydrogen, halogen, trifluoromethyl, C 1-6 alkyl, C 1-6 alkoxy, hydroxy and amino.
Claim 3
Dependent Claim 11 words
The method of claim 1 wherein said compound is alpha-phenyl-1-(2-phenyl)-4-piperidine methanol.
Claim 4
Dependent Claim 11 words
The method of claim 1 wherein said compound is alpha-phenyl-1-(3-phenpropyl)-4-piperidine methanol.
Claim 5
Dependent Claim 11 words
The method of claim 1 wherein said compound is alpha-(4-methylphenyl)-1-(2-phenethyl)-4-piperidine methanol.
Claim 6
Dependent Claim 11 words
The method of claim 1 wherein said compound is alpha-(4-methoxyphenyl)-1-(2-phenethyl)-4-piperidine methanol.
Claim 7
Dependent Claim 11 words
The method of claim 1 wherein said compound is alpha-(3,5-dimethylphenyl)-1-(2-phenethyl)-4-piperidine methanol.
Claim 8
Dependent Claim 11 words
The method of claim 1, wherein said compound is alpha-(3-(tifluoromethyl)phenyl-1-(2-phenethyl)-4-piperidine methanol.
Claim 9
Dependent Claim 11 words
The method of claim 1, wherein said compound is alpha-(2,3-dimethoxy)-1-(2-phenethyl)-4-piperidine methanol.
Claim 10
Dependent Claim 11 words
The method of claim 1, wherein said compound is alpha-(3,4-dichlorophenyl)-1-(2-phenylethyl)-4-piperidine methanol.

References Cited (Backward Citations)

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GB840704A Cited
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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) 1991-11-08 1992-05-09 1992-11-08 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1995-11-08 1996-05-09 1996-11-08 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1999-11-08 2000-05-09 2000-11-08 $7700.00 Window Closed / Lapsed

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