http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2120941-C1

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filingDate 1994-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_939cb87cf101c34005ab566293a23440
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publicationDate 1998-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2120941-C1
titleOfInvention Derivatives of quinolone carboxylic acid or their pharmaceutically acceptable salt
abstract FIELD: organic chemistry, chemical technology. SUBSTANCE: invention relates to new derivatives of quinolone carboxylic acid of the formula (I) , their pharmaceutically acceptable salts and hydrates where X means hydrocarbon group, fluorocarbon group or nitrogen atom; Y means hydrogen atom or methyl group; R 1 means hydrogen atom or C 1 -C 5 -alkyl group; R 2 means a group of the formula (a) where A and B mean fluorocarbon group or nitrogen atom at condition that when A is CF then B is N and when A is N then B is CF; R 3 means a group of the formula (b) where substitute R 4 means amino-group with racemate or (S)-enantiomer formation, or a group of the formula (c) where substituents R 5 , R 6 and R 7 mean hydrogen atom or C 1 -C 3 -alkyl group. Derivative of quinolone carboxylic acid of the formula (I) is synthesized by condensation of compound of the formula (II) and compound of the formula HR 3 in solvent in the presence of acid acceptor and excess of compound of the formula HR 3 that is one of reagents. Solvent is taken from a group involving pyridine, acetonitrile, N,N-dimethylformamide. In compound of the formula (II) and compound of the formula HR 3 substituents X, Y, Z, R 1 , R 2 and R 3 mean values indicated above. EFFECT: improved method of synthesis. 11 cl, 6 tbl, 29 ex
priorityDate 1993-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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