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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
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filingDate 1988-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d5a85268b453c3fa0b1bf5566c329a6d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eaf8f7d9ae8a1f635efd624268f5dbf6
publicationDate 1989-07-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H01180876-A
titleOfInvention Pyridine compound
abstract NEW MATERIAL:A pyridine compound of formula I (R 1 , R 2 are H, lower alkyl; R 3 is halogen; R 4 is isopropyl, tert.-butyl). n EXAMPLE: 4-(2-Chloronicotinoyl)-2,6-di-tert.-butylphenol. n USE: An intermediate of pyrazolopyridines having anti-inflammatory, analgesic, antipyretic, antiarthritic, antirheumatic and antiplatelet action. n PREPARATION: For example, a compound of formula II (X is halogen) is allowed to react with a compound of formula III under usual Friedel-Craft reaction conditions, namely in an inert solvent (such as dichloroethane or nitrobenzene) in the presence of a catalyst such as aluminum trichloride at a temperature of ice-cooling to the boiling point of the solvent to give the compound of formula I. n COPYRIGHT: (C)1989,JPO&Japio
priorityDate 1988-01-07-04:00^^<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: 32.