http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102605033-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_10b468b0922705a884eb13e179dec4de
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P35-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P35-06
filingDate 2012-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7efc89f3f66680b870454a6816f8d05
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_579b22ffe216b9af183001ca574beb20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e562099b035d7208e2c1c94f60eb1f1f
publicationDate 2013-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102605033-B
titleOfInvention Method for preparing cefazolin intermediate TDA
abstract The invention provides a method for preparing intermediate cefazolin TDA (7-amino-3-[(5-methyl-1,3,4-thiadiazol-2yl)thiomethyl]-3-cephalosporanicacid). The method comprises the following steps of: oxidizing cephalosporin C to be GL-7-ACA (glutaryl-7-aminocephalosporanic acid) by using D-amino acid oxidase; reacting with 2-methyl-5-sulfydryl-1,3,4-thiadiazole; removing glutaryl by using GL-7-ACA acylase to finally obtain TDA. The method provided by the invention improves a TDA synthetic route. By using reaction and synthesis based on the biological enzyme method, the method is green and environment-friendly and has no pollution. The problems in chemical production, such as large organic solvent using amount and long synthetic route, can be solved. Furthermore, thiadiazole can be recycled, so that the product quality is improved, the using amount of side chain is reduced, and the method is applicable to the industrial production.
priorityDate 2012-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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