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Outgoing Links

Predicate Object
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D499-87
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-87
filingDate 1997-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1998-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-19980077878-A
titleOfInvention 2-beta-imine-phenam derivatives and methods for their preparation
abstract Condensation reaction of the aldehyde represented by the general formula (IV) and the amine compound represented by the general formula (III) in the presence of a solvent to prepare an imine compound of the general formula (V) as an intermediate, and the imine represented by the general formula (V) The 2-beta-imine-phenam derivative represented by the novel general formula (I) is prepared by removing R 3 , which is a protecting group at the C-3 position of the compound, wherein the general formula (I) includes an isomer. Compound of formula (I) is a beta lactamase decontamination agent and is a useful compound that enhances antimicrobial activity when used in combination with an existing antibiotic in a certain ratio.n n n n n n n n In the formulas above, Q is hydrogen, methyl, cyanomethyl, carboxymethyl, alkoxycarbonylmethyl, dihydroxybenzyl derivative, allyl, acetyl derivative, amidoalkoxymethyl, 2-carboxyethoxy derivative, fluoroalkoxy Derivative, a pyridium acetyl derivative, R 3 is hydrogen, a carboxylate, a carboxy protecting group as a penicillin or cephalosporin compound such as 4-methoxybenzyl, diphenylmethyl, 4-nitrobenzyl and allyl. It is useful as a protecting group, n is an integer of 0-2.
priorityDate 1997-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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