http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H03176490-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/C07D463-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D463-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D463-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-435
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04
filingDate 1990-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4cb23477dc6b6abcc8592b812e23319c
publicationDate 1991-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H03176490-A
titleOfInvention (1-alkyl substituted) and (1,1-dialkyl substituted) carbacephalosporins
abstract NEW MATERIAL: A compound (salt) of formula I [A is H, an amino-protecting group, acyl, etc.; R 1 and R 2 are each H, a C 1-4 alkyl, etc.; R 3 is H a halogen, C 1-6 alkyl, (substd.) phenyl, etc.; R 4 is H, a carboxyl-protecting group, etc.; R 5 is H, a C 1-4 alkoxy, etc.]. n EXAMPLE: 5,5-Dimethyl-3-[(methylsulfonyl)oxy]-8-oxo-7-[(phenoxyacetyl)amino]-1 azabicyclo[4.2.0]octa-2-ene-carboxylic acid. n USE: Antibacterial agents effective against resistant microorganisms. n PROCESS: For example, 2,2-dimethyl-4-pentenal is reacted with benzylamine and then with 2-oxo-4-phenyl-3-oxazolidone acetyl chloride to give a compound of formula II. The product is hydrolysed to give an azetidinone compound of formula III, and the amino group in the product is protected. The protected product is oxidized, reacted with Masamune reagent and subjected to ring closure to give the compound of formula I. n COPYRIGHT: (C)1991,JPO
priorityDate 1989-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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