http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CS-239416-B1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9911f6de192c2b863a595ef9ae4b1723
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_190c620efffc60d8c098b4ec585ed1bb
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/F16C2300-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-34
filingDate 1984-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_56214ca34ca90fa4a33cde242c071401
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0a2b0ed9265d10366a4d881878067146
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e85a7d5dba931b61724030a6e48a473e
publicationDate 1986-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CS-239416-B1
titleOfInvention Process for the preparation of 7- (1H-tatrazol-1-yl) acetamidocalosporanic acid
abstract The present invention relates to a process for preparing 7-n- [1H-Tetrazol-1-yl] -acetamidocfaloaperanenacids of formula I and their saltsnβ organic bases and alkali metals.nN = NnN = CHnn-ch 2 -CO-NHnEnJ-CH2OCOCH3nČOOHnThe compound of formula I, in its formnsalts are used as an intermediate in productionnpolesynthotic antibiotics Cefazoline.nwhich has a broad spectrum of actionnagainst Oram-nogative and Oram-pazitivenbacteria.nA compound of formula I of the inventionnprepares 7-aminocephalospherate by acylation of saltsnof new acid with mixed acid anhydriden1H-tetrazal-1-yl-acetic acid and suitable tertiarynacid: [ce ^ -ΖΟΗ ^ / ^ Ι ^ Ο-ΟΟΟΗ, venwherein n is 0-16, in an organic solventnand an organic salt of the compoundnof formula I is isolated by addition of an organic onena solvent in which this is minimalnsoluble.
priorityDate 1984-03-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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