http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2915805-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-08
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-08
filingDate 2013-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f187e44aa689acb025d9665c0bf9a7d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a85035d966e8d547f289a6408d359bdb
publicationDate 2015-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2915805-A1
titleOfInvention Method for producing optically active bicyclic urea compound
abstract A problem to be solved by the present invention is to provide a process for producing an optically active bicyclic urea compound useful as an intermediate for ²-lactamase inhibitor, in a simple and easy manner with high efficiency. The present invention includes reacting a specific ester compound with a specific amine in the presence of a metal alkoxide and/or an alkaline earth metal salt to produce the corresponding amide compound, which is then reacted with phosgene or a phosgene equivalent, followed by, if necessary, treatment with an acid or a base, to produce an optically active bicyclic urea compound. This makes it possible to produce an optically active bicyclic urea compound in a simple and easy manner with high efficiency and in high optical purity, without using expensive reagents such as catalysts and condensation agents, and without passing through protection and deprotection steps.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109689611-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3489215-A4
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109689611-A
priorityDate 2012-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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