http://rdf.ncbi.nlm.nih.gov/pubchem/patent/IE-823036-L
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5929f2d6f4dba84be8dd3a8ba633db12 |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-395 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D205-085 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D205-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-397 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-425 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C- |
filingDate | 1982-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1983-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | IE-823036-L |
titleOfInvention | Azetidinones. |
abstract | NEW MATERIAL:The 4-cyano-2-azetidinone derivative of formulaI(R<1> is amino which may be acylated or protected; X is H or methoxy; W is H or sulfo). EXAMPLE:(3S, 4RS)-4-Cyano-3-tritylamino-2-azetidinone. USE:An intermediate of 4-substituted-2-azetidinone derivative, an antibacterial agent and a beta-lactamase-inhibiting agent. PROCESS:The compound of formulaIis prepared by reacting the compound of formula II[R<2> is same as R<1>; X is H or methody; W is H or sulfo; Y is halogen, group of formula -OCOR<3> (R<3> is hydrocarbon group), -SCOR<3>, or formula III (n is 1 or 2)]with a cyano compound, and if necessary, eliminating the protecting group from the product.n[JP58110563A] |
priorityDate | 1981-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 28.