http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H0625255-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2ca2e4410855da087e11bf3eea8933fa
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-59
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D501-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-59
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-00
filingDate 1993-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a15e3743ba6d24d5202b089a42f280d0
publicationDate 1994-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0625255-A
titleOfInvention Process for the preparation of 7-substituted amino-3-hydroxy-3-cephem-4-protected carboxy-sulfoxide ester
abstract (57) [Summary] [Objective] 3-exomethylenecepham-4-carboxy-sulfoxide ester, which is used for the purpose of streamlining the production of cephalosporin antibiotics such as cefachlor, was not isolated, and the intermediate complex was used as acetic acid. The feature is that it can be ozonized in ethyl or methylene chloride. The intermediate, which is a complex of 7-substituted amino-3-exomethylenecepham-4-carboxy-sulfoxide ester and a tin-containing Lewis acid-type Friedel-Crafts catalyst, is reacted with ozone under substantially anhydrous conditions. To provide a corresponding 3-hydroxy-3-cephem-4-carboxysulfoxide ester. Since the complex of this reaction is also formed in the synthetic reaction in which 3-chlorosulfinylazetidinone is ring-closed with a tin-containing Lewis acid type Friedel-Crafts catalyst, the above-mentioned reaction can be continuously carried out.
priorityDate 1992-04-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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