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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P3-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
filingDate 1994-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1999-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a6094e396359889fd83bbf43c9135fa
publicationDate 1999-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2126408-C1
titleOfInvention Triazolopyrimidine derivatives, a method of their synthesis, a fungicide composition, a method of struggle against fungi
abstract FIELD: organic chemistry, fungicides. SUBSTANCE: invention relates to derivatives of triazolopyrimidine of the general formula (I) where R 1 is possibly substituted alkyl, cycloalkyl or bicycloalkyl; R 2 is hydrogen atom; R 3 is a 3-4-membered heterocycle containing one S-atom; R 4 is halogen atom. Compounds are synthesized by interaction of a compound of the formula (II) where Hal - chlorine or bromine with a compound of the formula HN-R 1 R 2 and a compound of the formula (I) is synthesized where R 4 - chlorine or bromine atom followed by optionally reaction of the obtained compound (I) with fluorinated agent and producing a compound (I) where R 4 is fluorine atom. Compounds of the formula (I) exhibit activity against fungi of class ascomycetes, for example, Venturia inaequalis, Botrytis cinerea and Alternaria solani. EFFECT: improved method of synthesis, enhanced effectiveness of compounds. 11 cl, 2 tbl, 12 ex
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2524266-C1
priorityDate 1993-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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