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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-70
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-24
filingDate 2012-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2016-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103827087-B
titleOfInvention For preparing the improved method of 2-[(2E)-2-fluoro-2-(3-piperidylidene) ethyl]-1H-iso-indoles-1,3 (2H)-diketone
abstract The present invention relates to for preparation 2 [(2E) 2 fluorine 2 (3 piperidylidene) ethyl] 1H iso-indoles 1,3 (2H) diketone or a kind of improved method of its salt, this prepared compound is a kind of intermediate in the synthetic route of antibacterium compound 7 [(3E) 3 (2 amino 1 fluorine ethylidene) 1 piperidyl] 1 cyclopropyl 6 fluorine Isosorbide-5-Nitrae dihydro 8 methoxyl group 4 oxo 3 quinoline carboxylic acid.
priorityDate 2011-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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