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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 2013-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e38d4a4459bab50180191a4f7cc3532f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_123e512476d993e10bc4b56aaee958be
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_51b81a8a7f4f06f34161c97ece2aaa2b
publicationDate 2016-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-9388178-B2
titleOfInvention Process for the preparation of moxifloxacin hydrochloride
abstract The present invention relates to an improved and industriously advantageous process by means of providing coupling/condensing of wet mass of (1-cyclopropyl-6,7-difluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinoline carboxylic acid-O 3 ,O 4 )bis(acyloxy-O)borate with (S,S)-2,8-diazabicyclo[4.3.0]nonane to give 1-cyclopropyl-7-[S,S]-2,8-diazabicyclo-[4.3.0]non-8-yl)-6-fluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinoline carboxylic acid hydrochloride (Moxifloxacin hydrochloride) of Formula-I with high purity.
priorityDate 2012-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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