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filingDate 2006-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_16a89a2476ae00f34f0dd6ff70ea1000
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_53e11f07e4c5e20df5d553a120e19d63
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publicationDate 2007-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2007072868-A1
titleOfInvention Novel synthesis of gatifloxacin
abstract Provided are 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 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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