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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_10e4b1416c6e66e0ade5429212414964
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-56
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-56
filingDate 2003-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dc37fbd13f2a604683843a7e72047272
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_352aec51280e7403f15e8889623d49e6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_72a688dcc4eb8896dfc3680194158510
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f2d49c64d1421d218136e4862c540d2a
publicationDate 2004-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1478642-A1
titleOfInvention Synthesis of gatifloxacin
abstract Provided is a method for making (±)-1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinolenecarboxylic acid, commonly known as gatifloxacin, in very high purity, in a suspension in a dipolar aprotic solvent.
priorityDate 2002-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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