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filingDate 1996-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_58a241064ef6361cf4d267cfe02b5e17
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a18897bcc0bcb3907cf767cbb46fda9
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publicationDate 1999-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CZ-285878-B6
titleOfInvention 7 - ([1α, 5α, 6α] -6-amino-3-azabicyclo [3.1.0] hex-3-yl) -6-fluoro-1- (2,4-difluorophenyl) -1,4-dihydro salt -4-oxo-1,8-naphthyridine-3-carboxylic acid and methanesulfonic acid, process for its preparation and pharmaceutical compositions based thereon
abstract 7 - [[1.alpha., 5.alpha., 6.alpha.] - 6-amino-3-azabicyclo [3.1.0] -hex-3-yl] -6-fluoro-1- (2) salt, 4-difluorophenyl / -1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid and methanesulfonic acid, which contains the following major peaks in the X-ray powder diffraction pattern: peak 1: 2 theta /.degree C / Cu 4.5, distance d 19.5; peak # 2: 2 theta /.degree.C/ Cu 7.7, distance d 11.5; peak # 3: 2 theta /.degree.C/ Cu 9.1, distance d 9.7; peak # 4: 2 theta /.degree.C/ Cu 13.6, distance d 6.5; peak # 5: 2 theta /.degree.C/ Cu 15.0, distance d 5.9; peak # 6: 2 theta /.degree.C/ Cu 18.2, distance d 4.9; peak # 7: 2 theta /.degree.C/ Cu 18.6, distance d 4.8; peak # 8: 2 theta / Congestion Cu / Cu 22.8, distance d 3.9 exhibits advantageous stability so that it is suitable for the manufacture of antibacterial pharmaceutical compositions. This salt is produced from the corresponding salt, which does not exhibit the above characteristics , or a monohydrate thereof, by heating in the presence of an alcohol or a mixture thereof with an aprotic corrosion
priorityDate 1995-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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