http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2116304-C1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-08
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filingDate 1993-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_541f1b83fee61bd299653bf4b05a4372
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d19a73655325d2e1df4c4a2e06fec6d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f65f96910a6f7a4df55e4be151e605d1
publicationDate 1998-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2116304-C1
titleOfInvention Derivatives of azole, method of their synthesis, pharmaceutical composition
abstract FIELD: organic chemistry, heterocyclic compounds. SUBSTANCE: invention relates to the new derivatives of azole of the general formula (I): where Ar -halide; R 1 - - hydrogen or lower alkyl; R 3 - - lower alkyl possibly substituted with lower alkyl, halide, trifluoromethyl, lower alkoxy, halide (lower)-alkoxy, piperazinyl, benzylpiperazinyl, lower acylpiperazinyl, lower alkoxyphenylpiperazinyl being alkyl moiety of that can be substituted with halide, and Y and Z are independently nitrogen atom or methyne-group that can be optionally substituted additionally with lower alkyl-group, or its acid-additive salts exhibiting antifungal activity, and pharmaceutical composition based on thereof. The indicated compounds are synthesized by interaction of compounds of the formula (II) and (III) . The synthesized compounds can be used in medicine. EFFECT: improved method of synthesis, enhanced effectiveness of compounds synthesized. 29 cl, 34 tbl, 75 ex
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2460724-C2
priorityDate 1992-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 490.