http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S565483-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-12
filingDate 1979-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b13559d7efcfd4e3677ed78a00363682
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publicationDate 1981-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S565483-A
titleOfInvention Purification of cephalosporin compound
abstract PURPOSE: To obtain a purified cephalosporin compound useful as an antimicrobial or feed additive in a continuous process in high yield, by decomposing a crude cephalosporin compound with a salt in the presence of a specific organic solvent, and by oxidizing the freed compound. n CONSTITUTION: A crude cephalosporin compound of the formula (A is pyridyl ring; R is hydroxyl-substituted phenyl group; Het is 1W4C lower alkyl-substituted tetrazole; M is alkali metal, alkaline earth metal or organic amine salt) is decomposed with a slat in an amide solvent to give a crystalline free acid solvate compound. In this reaction, an organic alcohol or/and keton solvent is present in any stage. Methanol may be cited as the alcohol; acetone, as the ketone. n EFFECT: High purity enough to be administrable to a man or animal, and high yield. n COPYRIGHT: (C)1981,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6329372-B1
priorityDate 1979-06-25-04:00^^<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: 23.