http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H0331288-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D513-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-535
filingDate 1989-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_46675a6e36606026dc3d89ac8898923d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c6c6271aa7a69f61a193ad6881902d28
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publicationDate 1991-02-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0331288-A
titleOfInvention Production of 9,1-epoxymethano-7-fluoro-8-(4-methyl-1-piperazinyl)-5-oxo-5h-thiazolo(3,2-a)quinoline-4-carboxylic acid-hydrochloride in specific crystal form
abstract PURPOSE: To readily and surely obtain the subjective hydrochloride useful as an antibacterial agent without containing a compound of other crystal forms by treating a specific carboxylic acid with hydrochloric acid and heating the resultant hydrochloride together with ethanol under specific conditions. n CONSTITUTION: 9,1-Epoxymethano-7-fluoro-8-(4-methyl-1-piperazinyl)-5-oxo-5H- triazolo[3,2-a]quinoline-4-carboxylic acid is treated with hydrochloric acid to form a hydrochloride and 1 pt.wt. of the hydrochloride together with 1-40 pts.wt. of ethanol, is heated at 40°C to the boiling point of ethanol to afford the objective hydrochloride having at least six diffraction lines of 6.7±0.2, 10.3±0.2, 10.5±0.2, 16.1±0.2, 20.7±0.2 and 21.1±0.2 between 5-22 degree of diffraction angle 2θ in a X-ray diffraction spectrum with a reflective powder method using Cu-Kα radiation. n COPYRIGHT: (C)1991,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011031745-A1
priorityDate 1989-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 22.