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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04
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filingDate 2012-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4d1f91307200957d4c2228571d8251e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fefaa6472d42d66702af592efa42586c
publicationDate 2016-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EA-023617-B1
titleOfInvention IMPROVED METHOD OF OBTAINING 2 - [(2E) -2-Fluoro-2- (3-Piperidinilidene) Etyl] -1h-isoindol-1.3 (2h) -dione
abstract The invention relates to an improved method for producing 2 - [(2E) -2-fluoro-2- (3-piperidinylidene) ethyl] -1H-isoindole-1,3 (2H) -dione (compound (1)) or its salt, which is an intermediate in the chain of synthesis of antibacterial compound - 7 - [(3E) -3- (2-amino-1-fluoroethylidene) -1-piperidinyl] -1-chloropropyl-6-fluoro-1,4-dihydro-8-methoxy -4-oxo-3-quinolinecarboxylic 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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