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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-10
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C-
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D-
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-00
filingDate 1975-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1979-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84bff0dd1edb52f8141360c1d2b080fe
publicationDate 1979-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1056816-A
titleOfInvention Process for the conversion of 6-aminopenicillanic acid (6-apa) in 7-aminodesacetoxycephalosporanic acid (7-adca)
abstract ABSTRACT OF THE DISCLOSURE The present invention relates to a process for the conversion of 6-aminopenicillanic acid (6-APA) to 7-aminodesacetoxycephalosporanic acid (7-ACDA), the improvement comprises reacting one mole of a compound selected from the group consisting of alpha-chloro- and alpha-bromobenzyl penicillin-(s)-sulphoxide with from two to four moles of 3-trimethylsilyl-2-oxazolidinone (TMSO) at a temperature of between 60° and 120°C in an inert non-hydroxylic solvent and in the presence of thiourea and a compound selected from the group consisting of triethylamine, dimethylaniline, quinoline and picoline p-toluene sulfonate to obtain a solution, thereafter removing the solvent by evaporation, diluting the residue with water, adjusting the pH to 4.2, and isolating 7-amido-desacetoxycephalosporanic acid (7-ADCA).
priorityDate 1974-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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