http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109369681-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-04
filingDate 2018-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2020-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-109369681-B
titleOfInvention Preparation method of cefditoren pivoxil
abstract The invention relates to the technical field of antibiotic preparation, and particularly discloses a preparation method of cefditoren pivoxil, which comprises the steps of taking 7-amino-3-chloromethyl-3-cephem-4-carboxylic acid as an initial raw material, carrying out an aldehyde reaction of iodomethyl pivalate and carboxyl in a structure, carrying out a chloromethyl aldehyde reaction, a Grignard reaction and dehydration to obtain 7-ATCA trimethyl acetoxyl methyl ester, and carrying out amidation on the 7-ATCA trimethyl acetoxyl methyl ester and 2-methoxyimino-2- (2-aminothiazole-4-yl) acetic acid to obtain cefditoren pivoxil. The method has the advantages of high yield, low cost, short time consumption and environmental protection.
priorityDate 2018-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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