http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5639878-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D205-08
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B53-00
filingDate 1995-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_37a94f5ab44a9c027ddb1e4a5c5351b9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d55f70d834d35d07fe73e38e3cdbe423
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_06f2a240d2b60b7408689da7840685d3
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e3c06a4e7f16279e257c36d8ef155c06
publicationDate 1997-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5639878-A
titleOfInvention Acyloxylation process for preparing 4-acyloxy-2-azetidinone derivatives
abstract The present invention relates to a novel and improved process for preparing 4-acyloxy-2-azetidinone derivatives having the following formula (I) which are useful as an intermediate for synthesis of penem or carbapenem compounds: ##STR1## in which R 1 represents a hydroxy-protecting group; and R 3 represents an acyl group, which comprises reacting an azetidinone derivative having the following formula (II): ##STR2## wherein R 1 is defined as above and R 2 represents an alkyl group or an aryl group, with a N-haloacylimide in the presence of an organic carboxylic acid or a salt of an organic carboxylic acid. n The present invention uses the organic compound, N-haloacylimide, as the reactant rather than the heavy metal reactant used in the prior art, and thus provides an economical advantage and does not cause any problem related to safety and waste disposal after the reaction.
priorityDate 1994-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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