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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D499-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-897
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-87
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-00
filingDate 1991-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1994-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2465283daba12393cf1aea35ed16d82c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_990fc94caee86792fe9a0baa7a423df5
publicationDate 1994-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0524959-B1
titleOfInvention Process for sultamicillin intermediate
abstract PCT No. PCT/US91/01765 Sec. 371 Date Sep. 28, 1992 Sec. 102(e) Date Sep. 28, 1992 PCT Filed Mar. 15, 1991.A simplified method for making the chloromethyl ester of sulbactam in which the tetraalkylammonium sulbactam salt is not dried and isolated prior to alkylation. The method comprises reacting a tetraalkylammonium salt and a sulbactam salt in an aqueous solution to form an aqueous solution of tetraalkylammonium sulbactam. The tetraalkylammonium sulbactam is extracted into bromochloromethane or iodochloromethane, and water is removed from the organic layer to enhance the formation of the chloromethyl ester of sulbactam. The tetraalkylammonium sulbactam is reacted with bromochloromethane or iodochloromethane in the organic layer to form the chloromethyl ester of sulbactam.
priorityDate 1990-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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