http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5995289-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-02
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filingDate 1982-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fa60d88d2ba55246568e9dbbf7a4d6a
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publicationDate 1984-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5995289-A
titleOfInvention Triazolopyrimidine derivative, its preparation, and drug containing it as active ingredient
abstract NEW MATERIAL:A compound shown by the formula I [X 1 WX 3 are H, halogen, lower alkyl, lower alkoxy(carbonyl), carboxyl, OH, amino, nitro, or trifluoromethyl; R 1 is H, -CO 2 R 7 (R 7 is 1W6C alkyl); R 2 is -NR 8 R 9 , -NHNR 8 R 9 (R 8 and R 9 are H, 1W6C alkyl, etc.); when R 1 is H, R 3 and R 4 , and R 5 and R 6 are linked to form single bond, respctively; when R 1 is -CO 2 R 7 , R 3 and R 4 , and R 5 and R 6 are linked to form single bond, respectively, or R 3 and R 6 are H, and R 4 and R 5 are linked to form single bond, or R 3 and R 4 are linked to form single bond, and R 5 and R 6 are H]. n EXAMPLE: 7-( o-Chlorophenyl )-6-ethoxylcarbonyl-4, 5, 6, 7-tetrahydro-5-oxo[1, 2, 4] triazolo[1,5-a]pyrimidine. n USE: A remedy for diseases of circulatory organs. n PROCESS: A 5-halotriazolopyrimidine derivative shown by the formula II (Y is halogen) is reacted with an amino compound shown by the formula NR 5 R 9 or a hydrazino compound shown by the formula HNHNR 8 R 9 . n COPYRIGHT: (C)1984,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2623502-A1
priorityDate 1982-11-24-04:00^^<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: 29.