http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01258671-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_18a7d1606da2ec2ad08ae63822efb00e
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-02
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filingDate 1987-12-01^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_46ba7135935f0f01429ad99df35925c6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_efdeb09ab931fd71e4108f94fce8457b
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publicationDate 1989-10-16^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H01258671-A
titleOfInvention 5-(1h-imidazol-1-yl)-3(2h)-pyridazinone derivative
abstract NEW MATERIAL:A compound shown by formula I [R 1 is H, 1-14C alkyl, (halogen-substituted)benzyl, cinnamyl, naphthoxyethyl or (halogen-substituted) phenoxyethyl; R 2 is H or 1H-imidazolyl-1-yl; R 3 is H or (halogen-substituted) phenyl] or an acid addition salt thereof. n EXAMPLE: 5-(1H-imidazol-1-yl)-6-phenyl-3(2H)-pyridazinone. n USE: A drug useful as antithrombotic drug and antifungal agent having low toxicity and effective as a preventive and remedy of cerebral thrombosis, cerebral embolism, peripheral arterial and venous embolism and mycotic infection. n PREPARATION: For example, a 5-chloro-6-phenyl-3(2H)-pyridazinone derivative shown by formula II (R 4 and R 5 are H or Cl) is reacted with an excess amount of imidazole preferably in a solvent at 50-180°C for 1-8hr to give a compound shown by formula I wherein R 1 is H and R 3 is (halogen-substituted) phenyl. n COPYRIGHT: (C)1989,JPO&Japio
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priorityDate 1987-12-01^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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