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Pharmaceutical compositions containing 5,6,7,8-tetrahydroquinoline derivatives and related compounds

Assignee: John Wyeth and Brother Ltd
•
Filing: 1975-10-24
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Granted: 1977-08-23
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Expires: 1995-10-24
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Abstract

Abstract The invention relates to pharmaceutical compositions containing 5,6,7,8-tetrahydroquinoline-8-thioamides and nitriles and related tricyclic compounds and methods of treating ulcers using said compounds.

Inventors

  • 👤 Adrian Charles Ward Curran
  • 👤 Roger Crossley
  • 👤 David George Hill

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 06:19
CPC Classifications
C; C07; C07D; C07D215/00; C07D215/02; C07D215/04; C07D215/16; C07D215/20; C07D215/48; C07D219/00; C07D219/02; C07D219/04; C07D221/00; C07D221/02; C07D221/04

Claims Analysis

Total Claims: 15
Claim 1
Independent Claim 269 words
An anti-ulcer pharmaceutical composition comprising an effective amount of a compound of formula I ##STR11## or an acid addition salt thereof with a pharmaceutically acceptable acid, wherein R 1 , R 2 and R 6 are the same or different and are selected from hydrogen, trifluoromethyl, alkyl containing from 1 to 6 carbon atoms, phenylalkyl wherein the alkyl group has 1 - 6 carbon atoms, or phenyl groups or R 1 and R 2 taken together represent a polymethylene chain of 3 to 5 carbon atoms, R 7 represents hydrogen or from 1 to 3 groups selected from alkyl of 1 to 6 carbon atoms which may be substituted by alkoxy of 1 to 6 carbon atoms or trifluoromethyl, phenylalkyl wherein the alkyl group has 1 to 6 carbon atoms and phenyl groups, R 3 is hydrogen or alkyl of 1 to 6 carbon atoms, and any of the phenyl or the phenyl portion of any phenylalkyl groups R 1 , R 2 , R 6 and R 7 may be substituted by alkyl of 1 to 6 carbon atoms, lower alkoxy of 1 to 6 carbon atoms, halogen, nitro or trifluoromethyl with the provisos that (1) when R 1 and R 2 or R 2 and R 6 are both alkyl they are selected from normal and secondary alkyl groups and (2) when two alkyl R 7 groups are present on the same carbon atom then they are both n-alkyl groups and when two R 7 alkyl groups are present on adjacent carbon atoms they are selected from normal and secondary alkyl groups and a pharmaceutically acceptable carrier.
Claim 2
Dependent Claim 269 words
An anti-ulcer pharmaceutical composition comprising an effective amount of a compound of formula I ##STR11## or an acid addition salt thereof with a pharmaceutically acceptable acid, wherein R 1 , R 2 and R 6 are the same or different and are selected from hydrogen, trifluoromethyl, alkyl containing from 1 to 6 carbon atoms, phenylalkyl wherein the alkyl group has 1 - 6 carbon atoms, or phenyl groups or R 1 and R 2 taken together represent a polymethylene chain of 3 to 5 carbon atoms, R 7 represents hydrogen or from 1 to 3 groups selected from alkyl of 1 to 6 carbon atoms which may be substituted by alkoxy of 1 to 6 carbon atoms or trifluoromethyl, phenylalkyl wherein the alkyl group has 1 to 6 carbon atoms and phenyl groups, R 3 is hydrogen or alkyl of 1 to 6 carbon atoms, and any of the phenyl or the phenyl portion of any phenylalkyl groups R 1 , R 2 , R 6 and R 7 may be substituted by alkyl of 1 to 6 carbon atoms, lower alkoxy of 1 to 6 carbon atoms, halogen, nitro or trifluoromethyl with the provisos that (1) when R 1 and R 2 or R 2 and R 6 are both alkyl they are selected from normal and secondary alkyl groups and (2) when two alkyl R 7 groups are present on the same carbon atom then they are both n-alkyl groups and when two R 7 alkyl groups are present on adjacent carbon atoms they are selected from normal and secondary alkyl groups and a pharmaceutically acceptable carrier.
Claim 3
Dependent Claim 55 words
A pharmaceutical composition as claimed in claim 1, wherein the compound of formula I is one in which R 1 , R 2 , R 6 and R 7 are the same or different and are selected from hydrogen and lower alkyl of 1 to 4 carbon atoms, and R 3 is hydrogen or methyl.
Claim 4
Dependent Claim 35 words
A pharmaceutical composition as claimed in claim 1 wherein the compound of formula I is one in which R 1 , R 2 , R 3 and R 6 are selected from hydrogen and methyl.
Claim 5
Dependent Claim 36 words
A pharmaceutical composition as claimed in claim 1, wherein the compound of formula I is one in which R 1 ,R 2 and R 6 are selected from hydrogen and t-butyl and R 3 is hydrogen.
Claim 6
Dependent Claim 17 words
A pharmaceutical composition as claimed in claim 1 in which the compound of formula I is 3,4-dimethyl-5,6,7,8-tetrahydroquinoline-8-thiocarboxamide.
Claim 7
Dependent Claim 17 words
A pharmaceutical composition as claimed in claim 1 in which the compound of formula I is 2-methyl-5,6,7,8-tetrahydroquinoline-8-thiocarboxamide.
Claim 8
Dependent Claim 27 words
A pharmaceutical composition as claimed in claim 1 in which the compound of formula I is selected from 3-methyl-5,6,7,8-tetrahydroquinoline-8-thiocarboxamide and the pharmaceutically acceptable acid addition salts thereof.
Claim 9
Dependent Claim 17 words
A pharmaceutical composition as claimed in claim 1 in which the compound of formula I is 4-methyl-5,6,7,8-tetrahydroquinoline-8-thiocarboxamide.
Claim 10
Dependent Claim 17 words
A pharmaceutical composition as claimed in claim 1 in which the compound of formula I is 3-methyl-5,6,7,8-tetrahydroquinoline-8-(N-methyl)-thiocarboxamide.
Claim 11
Dependent Claim 17 words
A pharmaceutical composition as claimed in claim 1 in which the compound of formula I is 5,6,7,8-tetrahydroquinoline-8-thiocarboxamide.
Claim 12
Dependent Claim 25 words
A pharmaceutical composition as claimed in claim 1 in which the compound of formula I is 3,6-dimethyl-5,6,7,8-tetrahydroquinoline-8-thiocarboxamide or a pharmaceutically acceptable acid addition salt thereof.
Claim 13
Dependent Claim 25 words
A pharmaceutical composition as claimed in claim 1 in which the compound of formula I is 3,5-dimethyl-5,6,7,8-tetrahydroquinoline-8-thiocarboxamide or a pharmaceutically acceptable acid addition salt thereof.
Claim 14
Dependent Claim 16 words
A pharmaceutical composition as claimed in claim 1 wherein the compound of formula I is sym-octahydroacindine-4-thiocarboxamide.
Claim 15
Dependent Claim 33 words
A method of treating ulcers in an afflicted host, which method comprises orally administering to the said host a therapeutically effective amount of a compound of formula 1 as defined in claim 1.

References Cited (Backward Citations)

US3823152A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1980-08-22 1981-02-21 1981-08-23 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-08-22 1985-02-21 1985-08-23 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-08-22 1989-02-21 1989-08-23 $7700.00 Window Closed / Lapsed

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