http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H02129181-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-50
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-02
filingDate 1988-11-04^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6530795c59f117490f62a4a12d9ccb55
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_18719d12cf8dffd0b16a848d8289e30a
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publicationDate 1990-05-17^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H02129181-A
titleOfInvention 1-aryl-4-(1h-imidazol-1-yl)phthalazine derivative
abstract NEW MATERIAL:1-Aryl-4-(1H-imidazol-1-yl)phthalazine derivative or formula I (R is lower alkoxyphenyl, allyloxyphenyl, pyridylmethyloxyphenyl, benzyloxyphenyl, furil which may have substituent, thienyl or naphthyl). n EXAMPLE: 1-(1H-imidazol-1-yl)-4-(4-ethoxyphenyl)phthalazine. n USE: Useful as a platelet aggregation inhibitor with high safety excellent in effect and capable of oral and parenteral administrations. n PREPARATION: For example various alkyl halide derivatives are reacted with a compound of formula II i n an amount of equimolar-two time moles of that of the compound using a basic compound as a dehalogenation agent at room temperature - 50°C as shown by the reaction formula to obtain the objective compound of formula I. n COPYRIGHT: (C)1990,JPO&Japio
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priorityDate 1988-11-04^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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