http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7507812-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-24
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-24
filingDate 2004-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_713f0bd48ac9d73ccdd9665dd6b06077
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_967ee82a8a8242e2a7e5946e1dc1be39
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d067848e57b63c33c113db34a0cb6f41
publicationDate 2009-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7507812-B2
titleOfInvention Process for producing 3-chloromethyl-3-cephem derivatives
abstract An industrially advantageous process for producing 3-chloromethyl-3-cephem derivative crystals. The process for 3-chloromethyl-3-cephem derivative production comprises: a first step in which a thiazolineazetidinone derivative (1) is reacted with a sulfonyl halide (2) in the presence of an acid in a solvent to obtain an azetidinone derivative (3); a second step in which the azetidinone derivative (3) is reacted with a chlorinating agent in an organic solvent to obtain a chlorinated azetidinone derivative (4); and a third step in which the chlorinated azetidinone derivative (4) is reacted with an alcoholate (5) at a pH of 8 or lower in a solvent comprising an alcohol and an ether and a 3-chloromethyl-3-cephem derivative (6) is recovered in the form of crystals.
priorityDate 2003-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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