US4975445A
Expired / Lapsed
US
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Substituted cyclohexenes as central nervous system agents
Assignee: Warner Lambert Co LLC
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Filing: 1989-12-06
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Granted: 1990-12-04
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Expires: 2009-12-06
Abstract
Abstract Substituted cyclohexenes are described, as well as methods for the preparation and pharmaceutical composition of same, which are useful as central nervous system agents and are particularly useful as dopaminergic, antipsychotic, and antihypertensive agents as well as for treating hyperprolactinaemia-related conditions and central nervous system disorders.
Inventors
- 👤 Bradley W. Caprathe
- 👤 Juan C. Jaen
- 👤 Sarah J. Smith
- 👤 Lawrence D. Wise
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-03 09:09
CPC Classifications
C; C07; C07D; C07D295/00; C07D295/04; C07D295/12; C07D213/00; C07D213/02; C07D213/04; C07D213/60; C07D213/72; C07D213/74; A; A61; A61K; A61K31/00; A61K31/33; A61K31/395; A61K31/435; A61K31/44; A61P; A61P15/00; A61P25/00; A61P25/14; A61P25/18; A61P25/24; A61P25/26; A61P43/00; A61P9/00; A61P9/12; C07D401/00; C07D401/02; C07D401/08; C07D409/00; C07D409/02; C07D409/08; C07D409/12; C07D417/00; C07D417/02; C07D417/12
Claims Analysis
Total Claims: 7
Claim 1
Independent Claim
164 words
A compound of Formula I ##STR29## wherein p1 R 1 is phenyl, phenyl substituted by one to four substituents selected from the group consisting of lower alkyl, lower alkoxy, lower thioalkoxy, halogen, and trifluoromethyl, 2-, 30, or 4-pyridinyl or 2-, 3-, or 4-pyridinyl substituted by lower alkyl, lower alkoxy, or halogen, 2-, 4-, or 5-pyrimidinyl or 2-, 4-, or 5-pyrimidinyl substituted by lower alkyl, lower alkoxy, or halogen, 2-pyrazinyl or 2-pyrazinyl substituted by lower alkyl, lower alkoxy, or halogen, 2- or 3-thienyl or 2- or 3-thienyl substituted by lower alkyl or halogen, 2- or 3-furanyl or 2- or 3-furanyl substituted by lower alkyl or halogen, 2-, 4-, or 5-thiazolyl or 2-, 4-, or 5-thiazolyl substituted by lower alkyl or halogen; m is zero or an integer from one to two; R 2 is ##STR30## wherein R 1 is as defined above; n is zero or an integer from one to four; and corresponding optical isomers thereof; or a pharmaceutically acceptable acid addition salt thereof.
Claim 2
Dependent Claim
164 words
A compound of Formula I ##STR29## wherein p1 R 1 is phenyl, phenyl substituted by one to four substituents selected from the group consisting of lower alkyl, lower alkoxy, lower thioalkoxy, halogen, and trifluoromethyl, 2-, 30, or 4-pyridinyl or 2-, 3-, or 4-pyridinyl substituted by lower alkyl, lower alkoxy, or halogen, 2-, 4-, or 5-pyrimidinyl or 2-, 4-, or 5-pyrimidinyl substituted by lower alkyl, lower alkoxy, or halogen, 2-pyrazinyl or 2-pyrazinyl substituted by lower alkyl, lower alkoxy, or halogen, 2- or 3-thienyl or 2- or 3-thienyl substituted by lower alkyl or halogen, 2- or 3-furanyl or 2- or 3-furanyl substituted by lower alkyl or halogen, 2-, 4-, or 5-thiazolyl or 2-, 4-, or 5-thiazolyl substituted by lower alkyl or halogen; m is zero or an integer from one to two; R 2 is ##STR30## wherein R 1 is as defined above; n is zero or an integer from one to four; and corresponding optical isomers thereof; or a pharmaceutically acceptable acid addition salt thereof.
Claim 3
Dependent Claim
63 words
A compound according to claim 1, in which R 1 is phenyl, phenyl substituted by para-lower alkyl, para lower alkoxy, para lower thioalkoxy, or para halogen, 2-, 3-, or 4-pyridinyl, 2-, or 3-furanyl, 2- or 3-thienyl, or 2-, 4-, or 5-thiazolyl; m is zero; ##STR31## wherein R 1 is as defined above; and n is zero or an integer from one to three.
Claim 4
Dependent Claim
52 words
A compound according to claim 2, in which R 1 is phenyl, phenyl substituted by para-lower alkoxy or para-halogen, 2-, 3-, or 4-pyridinyl, 2or 3-thienyl, or 2-, 4-, or 5-thiazolyl; m is zero; ##STR32## wherein R 1 is as defined above; and n is zero or an integer from one to two.
Claim 5
Dependent Claim
28 words
A compound according to claim 3 selected from the group consisting of: (±)-(2-Pyridinyl)-4-[4-(2-pyridinyl)-3-cyclohexen-1-yl]piperazine; (±)-1-(2-Pyridinyl)-4-[4-(3-pyridinyl)-3-cyclohexen-1-yl]piperazine; (±)-1-(2-Pyridinyl)-4-[4-(2-thienyl)-3-cyclohexen-1-yl]piperazine; (±)-1-(2-Pyridinyl)-4-[4-(3-thienyl)-3-cyclohexen-1-yl]piperazine; (±)-1-(4-Phenyl-3-cyclohexen-1-yl)-4-(2-pyridinyl)piperazine; (±)-1-(2-Pyridinyl)-4-[4-(2-thienyl)-3-cyclohexen-1-yl]methyl]piperazine; (±)-1-(2-Pyridinyl)-4-[[4-(2-pyridinyl)-3-cyclohexen-1-yl]methyl]piperazine; (±)-1-(2-Pyridinyl)-4-[4-phenyl-3-cyclohexen1-yl]methyl]piperazine; (±)-1-(2-Pyridinyl)-4-[2-[4-(2-thienyl)-3-cyclohexen-1-yl]ethyl]piperazine; (±)-1-[2-(4-Phenyl-3-cyclohexen-1-yl)ethyl]-4-(2-pyridinyl)piperazine; (±)-1-(2-Pyridinyl)-4-[2-[4-(2-pyridinyl)-3-cyclohexen-1-yl]ethyl]piperazine; (±)-1-[2-[4-(4-Fluorophenyl)-3-cyclohexen-1-yl]-ethyl]-4-(2-pyridinyl)piperazine; (±)-1-(2-Pyridinyl)-4-[2-[4-(2-thiazolyl)-3-cyclohexen-1-yl]ethyl]piperazine; (±)-1,2,3,6-Tetrahydro-4-phenyl-1-[2-[4-(2-thienyl)3-cyclohexen-1-yl]-ethyl]pyridine; and (±)-2-[4-(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)-1-cyclohexen-1-yl]pyridine.
Claim 6
Dependent Claim
27 words
A method of treating schizophrenia comprising administering to a host suffering therefrom a therapeutic effective amount of a compound according to claim 1 in unit dosage form.
Claim 7
Dependent Claim
36 words
A pharmaceutical composition adapted for administration as a dopaminergic, antipsychotic, antihypertensive or antidepressant agent comprising a therapeutic effective amount of a compound according to claim 1 in admixture with a pharmaceutically acceptable excipient, diluent or carrier.
References Cited (Backward Citations)
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