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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_da54f7ebbd2d9d8a82f92aca4d1b4e48
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D285-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-06
filingDate 1979-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1982-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_65b67e47a5a01d91a22e2f5af738ea59
publicationDate 1982-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1137495-A
titleOfInvention Process for the manufacture of 5-mercapto- 1,2,3-triazoles
abstract ABSTRACT Process for the manufacture of 5-mercapto-1, 2, 3-triazoles 5-Mercapto-1,2,3-triazoles of the formula I (I) (in which R1 represents H or optionally substituted C1-C4-alkyl), suitable as starting materials for the production of antibiotics, preferably cephalosporin derivatives, are prepared by reacting a 1,2,3-thiadiazole-4-R1-5-carboxylic acid azide with an alcohol or phenol to form a (1,2,3-thiadiazol-4-R1-5-yl)-carbamic acid ester, hydrolysing the carbamic acid ester in the presence of an acid or base to form a 5-amino-4-R1-1,2,3-thiadiazole and rearranging the 5-amino-4-R1-1,2,3-thiadiazole in the presence of a base.
priorityDate 1978-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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