http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110128449-B

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P17-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P17-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-22
filingDate 2019-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-110128449-B
titleOfInvention 7-Phenylacetamido-3-deacetoxycephalosporanate and its preparation method and application
abstract The present invention relates to 7-phenylacetamido-3-deacetoxy cephalosporanate and its preparation method and application. Described 7-phenylacetamido-3-deacetoxy cephalosporanate, its structural formula is as follows: wherein M + is selected from metal ions or ammonium ions. A method for preparing 7-phenylacetamido-3-deacetoxy cephalosporanic acid salt, comprising the steps of: reacting 7-phenylacetamido-3-deacetoxy cephalosporanic acid with an alkaline salt-forming agent to obtain; Or by reacting 7-phenylacetamido-3-deacetoxy cephalosporanic acid trimethylsilyl ester with an alkaline salt-forming agent. 7-ADCA can be prepared from 7-phenylacetamido-3-deacetoxycephalosporanate, and the content of the obtained 7-ADCA product is very high, especially the content of the isomer △2-7-ADCA Below 0.5%, it is more suitable for synthesizing high-quality cephalosporin APIs such as cephalexin, cefradine, cefadroxil, and ceftazime pivoxil.
priorityDate 2019-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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