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filingDate 1996-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c9b3314ddaf2dfe5bf7b78b62e147ad6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_22ce03fb6d391d670eec0d940f14817e
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publicationDate 1999-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2143433-C1
titleOfInvention Pyrido[3,2-e]pyrazinones, methods of preparation thereof, preparation based on these compounds, and method of their preparation
abstract FIELD: organic synthesis and biologically-active compounds. SUBSTANCE: invention provides new pyrido[3,2-e] pyrazinones of general formula I: (I), wherein X, Y, and Z are nitrogen or group CR 3 , provided that at least one of X, Y, Z is nitrogen; R 1 is optionally aryl- substituted C 1 -C 10 -alkyl; R 2 hydrogen, C 5 -C 7 -cycloalkyl, or C 1 -C 10 -alkyl optionally substituted by radical selected from group including aryl, aryloxy, hydroxyl, sulfonyl, pyridyl, and quinolyl; A is methylene, group NR 3 , or oxygen atom; R 3 hydrogen or C 1 -C 6 -alkyl; or their physiologically tolerable salts exhibiting anti-asthmatic and antiallergenic effects. EFFECT: increased choice of pharmaceutically active compounds. 8 cl, 2 tbl, 53 ex
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