http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H08325261-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-06
filingDate 1995-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_433a2bbdd09865f7fcc451503d66f652
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9b35d424955a3c1b6170bfa6b1010ed6
publicationDate 1996-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H08325261-A
titleOfInvention Method for producing azetidinone compound
abstract (57) [Summary] [Structure] Formula [I] (In the formula, R 1 represents a lower alkyl group which may be substituted with an optionally protected hydroxyl group, R 2 represents a hydrogen atom, an easily removable amino protecting group, an alkoxycarbonylmethyl group or a phenoxycarbonylmethyl group. , R 3 represents a hydrogen atom, or an optionally substituted lower alkyl group.), An azetidinone compound represented by the formula [II] embedded image (In the formula, R 1 , R 2 and R 3 have the same meanings as described above.) The manufacturing method of the compound represented by. [Effect] In the production according to the present invention, by using phosgene as an intermediate of a carbapenem compound useful as an antibacterial agent, which is industrially inexpensive and easy to use, the wastewater in the post-treatment is compared with other "carboxylic acid activators". It can be manufactured and supplied industrially advantageously at low cost without increasing the load and complicating the operation.
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priorityDate 1995-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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