http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102977089-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c9d77c2320308698bbf72fdec0ed40d4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9ea6af237c451ba39f93109f83a3c4d8
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12
filingDate 2012-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc45545f0193b54aab24d76427bc8f5e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8a129620563192d4b83beea4382b1eb1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b82fd229a2fce66081dbcf653af2c14e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b501874e70e6a632207a173934a09ff0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_224f9670975c166a17491d66709197af
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_66f017af3de2dd84cbea89c142d9be88
publicationDate 2015-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102977089-B
titleOfInvention Method for preparing high-purity cefdinir antibiotic 7-side chain synthesis critical material
abstract The invention discloses a method for preparing a high-purity cefdinir antibiotic 7-side chain synthesis critical material. The method comprises the following steps of: by taking demethylated ethyl 2--2-methoxyiminoacetate and triphenylcarbinol as raw materials, taking a carbonic ester solvent as a solvent, taking a dimethyl carbonate boron trifluoride solid complex as a catalyst, preparing (Z)-2-(2-amino-4-thiazolyl)-2-benzyltrimethylimineethyl acetate; adding an inorganic alkali solution into an alcohol solvent to carry out a hydrolysis reaction, acidizing the solution by utilizing inorganic acid after the hydrolysis reaction is finished, and preparing (Z)-2-(2-amino-4-thiazolyl)-2-benzyltrimethylimineacetic acid; by taking the (Z)-2-(2-amino-4-thiazolyl)-2-benzyltrimethylimineacetic acid and DM as raw materials and a pyridines compound as a catalyst in a halogenated alkane solvent, dripping mixed solution of triethyl phosphate and triethylamine, and preparing the MEAT. The reaction process is easy to operate, and the used solvent is low in toxicity, environment-friendly, easy to recycle, high in yield, low in cost and suitable for industrialization.
priorityDate 2012-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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