GB1172426A - Imidazo-(1,5-a)-quinoline Derivatives - Google Patents

Imidazo-(1,5-a)-quinoline Derivatives

Info

Publication number
GB1172426A
GB1172426A GB613067A GB613067A GB1172426A GB 1172426 A GB1172426 A GB 1172426A GB 613067 A GB613067 A GB 613067A GB 613067 A GB613067 A GB 613067A GB 1172426 A GB1172426 A GB 1172426A
Authority
GB
United Kingdom
Prior art keywords
lower alkyl
piperazinyl
pyrrolidinyl
compound
formula
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB613067A
Inventor
William Wrights Jr
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB1172426A publication Critical patent/GB1172426A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

1,172,426. Imidazo - (1,5-a) - quinoline derivatives. AMERICAN CYANAMID CO. 8 Feb., 1967 [18 Feb., 1966], No. 6130/67. Heading C2C. Novel compounds of Formula I or a pharmaceutically acceptable acid addition salt thereof; wherein R and R 1 are hydrogen, halogen, lower alkyl, lower alkoxy or trifluoromethyl; R 2 is hydrogen, lower alkyl or halogen, Y is oxygen or sulphur; n is an integer from 1 to 4; and R 3 and R 4 are hydrogen, lower alkyl, lower alkenyl, cycloalkyl, aralkyl, or lower (cycloalkyl) methyl, or -NR 3 R 4 , when taken together, is 1-pyrrolidinyl, lower alkyl-1-pyrrolidinyl, piperidino, lower alkylpiperidino, morpholino, lower alkylmorpholino, hexamethyleneimino, 1-piperazinyl, 1 -(lower alkyl) -4-piperazinyl, 1 -(hydroxy lower alkyl)-4-piperazinyl, 1 - (lower alkanoyloxyalkyl) - 4 - piperazinyl- 1 - phenyl - 4 - piperazinyl, 1 - (lower alkoxyphenyl) - 4 - piperazinyl, 1 - trifluoromethyl, phenyl - 4 - piperazinyl, 1 - (lower alkylphenyl)- 4 - piperazinyl, 1 - halophenyl - 4 - piperazinyl, 4 - phenyl - 1,2,4,5 - tetrahydro - 1 - pyridinyl, 4 - alkylphenyl - 1,2,5,6 - tetrahydro - 1- pyridinyl, 4 - halophenyl - 1,2,5,6 - tetrahydro- 1 - pyridinyl, 4 - lower alkoxyphenyl - 1,2,5,6- tetrahydro - 1 - pyridinyl, 4 - trifluoromethylphenyl - 1,2,5,6 - tetrahydro - 1 - pyridinyl or azabicyclo - [3.2.2] - nonan - 3 - yl; or -C n H 2n - NR 3 R 4 , when taken together, is (2-pyrrolidinyl)- lower alkyl, (3-pyrrolidinyl) lower alkyl, (1- lower alkylpyrrolidinyl) lower alkyl, (1-benzylpyrrolidinyl) - lower alkyl, [1 - (halobenzyl)- pyrrolidinyl - lower alkyl, (1 - lower alkylpyrrolidinyl) - lower alkyl, (1 - benzylpyrrolidinyl) - lower alkyl, [1 - (halobenzyl) - pyrrolidinyl] - lower alkyl, [1 - (lower alkoxybenzyl)- pyrrolidinyl] - lower alkyl, [1 - (lower alkylbenzyl) - pyrrolidinyl] - lower alkyl, piperidinyl lower alkyl, (1-lower alkyl piperdinyl)- lower alkyl, (1 -benzylpiperidinyl)-lower alkyl, [1 - (halobenzyl) - piperidinyl] - lower alkyl, [1 - (lower alkoxybenzyl) - piperidinyl] - lower alkyl, or [1 - (lower alkylbenzyl) - piperidinyl]- lower alkyl and radicals qualified by the term " lower " contain up to 4 carbon atoms are prepared either (a) by heating a compound of Formula II wherein Z is H or -C n H 2n X wher X is halogen, (C 1 -C 4 ) alkylsulphonyloxy or arylsulphonyloxy, (1) when Z is H, with a compound of formula X-C n H 2n NR 3 R 4 or (2) when Z is C n H 2n X 1 with a compound of formula H-NR 3 - R 4 , in both eases optionally followed by reacting the product with P 2 S 5 and/or salt formation and/or removal of a group R 3 is benzyl by hydrogenolysis or (b) reacting a compound of formula with a cyclizing agent providing a carbonyl or thioketone group such as phosgene, thiophosgene, ethyl chloroformate or N,N<SP>1</SP>-carbonyl diimidazole or (c) where n is 1 by reaction of a compound of Formula II above with formaldehyde/formic acid and a compound of formula HNR 3 R 4 . 2 - (3 - Bromopropyl) - 3,3a,4,5 - tetrahydroimidazo - [1,5-a] - quinolin - 1 - (2H) - one is prepared by reaction of 1,3-dibromopropane and the 2-unsubstituted compound. Pharmaceutical compositions in conventional forms for oral administration and having tranquilizing activity comprise an above novel compound or salt and a carrier therefor.
GB613067A 1966-02-18 1967-02-08 Imidazo-(1,5-a)-quinoline Derivatives Expired GB1172426A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US52835466A 1966-02-18 1966-02-18

Publications (1)

Publication Number Publication Date
GB1172426A true GB1172426A (en) 1969-11-26

Family

ID=24105342

Family Applications (1)

Application Number Title Priority Date Filing Date
GB613067A Expired GB1172426A (en) 1966-02-18 1967-02-08 Imidazo-(1,5-a)-quinoline Derivatives

Country Status (9)

Country Link
BE (1) BE694205A (en)
CH (1) CH521366A (en)
DE (1) DE1645955A1 (en)
ES (1) ES336999A1 (en)
FR (2) FR1511914A (en)
GB (1) GB1172426A (en)
IL (1) IL27396A (en)
NL (1) NL6702347A (en)
SE (1) SE335345B (en)

Also Published As

Publication number Publication date
BE694205A (en) 1967-08-17
SE335345B (en) 1971-05-24
DE1645955A1 (en) 1970-07-16
FR1511914A (en) 1968-02-02
IL27396A (en) 1971-03-24
ES336999A1 (en) 1968-06-01
NL6702347A (en) 1967-08-21
FR6101M (en) 1968-06-10
CH521366A (en) 1972-04-15

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Legal Events

Date Code Title Description
PS Patent sealed
PLNP Patent lapsed through nonpayment of renewal fees