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filingDate 1987-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82d47e3851d9c6915e766c54b97af0e4
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publicationDate 1987-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0233800-A1
titleOfInvention Imidazo[1,2-a]quinoline derivatives, their preparation and therapeutical use thereof
abstract X représente l'hydrogène, un halogène ou un groupe (C 1 - 4 )alkyle, (C 1-4 )alcoxy, (C 1 4 )alkylthio, méthylsulfonyle, amino, (C 1-4 )alkylamino, di-(C 1-4 )alkylamino, nitro ou trifluoroalkyle, Y représente l'hydrogène, un halogène ou un groupe méthyle en position 6, 7 ou 8 et, R1 et R2 pris séparément, représentent chacun l'hydrogène ou un groupe (C 1-6 )alkyle, ou bien R1 et R2 forment ensemble und chaîne tétraméthylène, pentaméthylène, méthyl-3 aza-3 pentaméthylène ou oxa-3 p e ntaméth y lè ne, nainsi que leurs sels d'addition acceptables en pharmacologie.Compounds corresponding to the general formula (I) in which X represents hydrogen, a halogen or a (C 1 - 4 ) alkyl, (C 1-4 ) alkoxy, (C 1 4 ) alkylthio, methylsulfonyl, amino, (C 1-4 ) alkylamino, di- (C 1-4 ) alkylamino, nitro or trifluoroalkyl, Y represents hydrogen, a halogen or a methyl group in position 6, 7 or 8 and, R1 and R2 taken separately, each represent hydrogen or a (C 1-6 ) alkyl group, or else R1 and R2 together form a tetramethylene, pentamethylene, 3-methyl-3-aza-3 pentamethylene or oxa-3 p e ntameth y lene chain , as well as their addition salts acceptable in pharmacology.n n n Application in therapy.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2759700-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9700074-A1
priorityDate 1986-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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