http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105017284-A

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filingDate 2015-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_467da6bdcfbcf8e6ad7025eab72494c9
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publicationDate 2015-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105017284-A
titleOfInvention The preparation method of ceftizoxime propivoxil and its intermediate and the preparation method of the intermediate
abstract The invention discloses a method for preparing ceftizoxime propivoxil by using a mixed acid anhydride method, an intermediate 3a/3b/3c and a preparation method for the intermediate. React aminothioxime acetates with BOC-alanine by mixed anhydride method in an organic solvent, and then hydrolyze under organic alcohol conditions to generate intermediates 3a/3b/3c, which are carried out with 7-ANCA in an organic solvent Condensation reaction, esterification to obtain BOC-alanyl ceftizoxime acid, react with halogenated pivalate methyl ester in the presence of acid binding agent to prepare BOC-alanyl ceftizoxime valproxil, remove BOC Protecting group, concentrated and crystallized in an organic solvent to obtain the target compound ceftizoxime propivoxil. The invention has the characteristics of cheap and easy-to-obtain raw materials, mild reaction conditions, less by-products, reliable purity, high yield, and easy large-scale industrial production.
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Total number of triples: 33.