← Back to Patent Explorer
US3971789A Expired / Lapsed US ⏱️ 0.0 years remaining

O-(4-Quinolylamino)benzamides

Assignee: John Wyeth and Brother Ltd
•
Filing: 1975-01-23
•
Granted: 1976-07-27
•
Expires: 1995-01-23
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract The disclosure describes new 4-aminoquinoline derivatives of general formula ##SPC1## And their acid addition salts, where X is a halogen atom or a trifluoromethyl group, Z is a hydrogen atom or a defined substituent, R is group of the formula --R.sub.3 N--A--NR.sub.1 R.sub.2 (II), ##SPC2## where A in formula II is a chain of 1 to 5 methylene groups which may be substituted with alkyl, the ring in formula IIIa and IIIb is a piperidine or pyrrolidine ring that may be substituted with alkyl and R 1 , R 2 and R 3 represent hydrogen or certain defined substituents. The new 4-aminoquinoline derivatives show anti-malarial activity and, in some cases, show one or more of the following activities:- anti-inflammatory activity, anti-hypertensive activity, anti-trichomonal activity, inhibition of blood platelet aggregation, anti-ulcer activity and activity against allergic asthma. Compounds where --COR is in the o-position with respect to the 7-(halo or trifluoromethyl)-4-quinolylamino group and R is di(lower alkyl)aminopiperidino or --NR 10 R 11 where R 10 is hydrogen or lower alkyl and R 11 is di(lower alkyl)amino(lower alkyl) or 1-(lower alkyl)piperidyl show anti-inflammatory activity.

Inventors

  • 👤 John Leheup Archibald
  • 👤 John Terence Arnott Boyle
  • 👤 John Christopher Saunders

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-31 02:04
CPC Classifications
C; C07; C07D; C07D215/00; C07D215/02; C07D215/16; C07D215/38; C07D215/42; C07D215/44

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 73 words
A compound selected from those having the formula ##SPC16## and their pharmaceutically acceptable acid addition salts, wherein X is selected from halogen and trifluoromethyl; Z is selected from the group consisting of hydrogen, halogen and lower alkyl; and R is selected from di(lower alkyl)aminopiperidino and a group having the formula ##EQU3## wherein R 10 is selected from hydrogen and lower alkyl and R 11 is selected from di(lower alkyl)amino(lower alkyl) and 1-(lower alkyl)piperidinyl.
Claim 2
Dependent Claim 73 words
A compound selected from those having the formula ##SPC16## and their pharmaceutically acceptable acid addition salts, wherein X is selected from halogen and trifluoromethyl; Z is selected from the group consisting of hydrogen, halogen and lower alkyl; and R is selected from di(lower alkyl)aminopiperidino and a group having the formula ##EQU3## wherein R 10 is selected from hydrogen and lower alkyl and R 11 is selected from di(lower alkyl)amino(lower alkyl) and 1-(lower alkyl)piperidinyl.
Claim 3
Dependent Claim 20 words
A compound as defined in claim 1 which is selected from 2-(7-chloro-4-quinolylamino)-N-(1-ethyl-3-piperidyl)benzamide and the pharmaceutically acceptable acid addition salts thereof.
Claim 4
Dependent Claim 20 words
A compound as defined in claim 1 which is selected from 2-(7-chloro-4-quinolylamino)-N-(2-diethylaminoethyl)-N-ethylbenzamide and the pharmaceutically acceptable acid addition salts thereof.
Claim 5
Dependent Claim 20 words
A compound as defined in claim 1 which is selected from 2-(7-chloro-4-quinolylamino)-N-(2-diethylaminoethyl)benzamide and the pharmaceutically acceptable acid addition salts thereof.

References Cited (Backward Citations)

US3875165A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-07-27 1980-01-26 1980-07-27 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-07-27 1984-01-26 1984-07-27 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-07-27 1988-01-26 1988-07-27 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag