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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D261-06
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-04
filingDate 1993-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1994-01-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f973a4207ce94e1de15fa83583d24a18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0c5de1deac8201c4757e6fb663a16030
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_76c0e22fd61c0beef1a1ff9d7ee2a948
publicationDate 1994-01-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5276160-A
titleOfInvention Preparation of 3-carbamoylisoxazole-4-carboxylic esters by selective amidation
abstract Abstract of the Disclosure: 3-Carbamoylisoxazole-4-carboxylic esters of the formula I <IMAGE> I where R1 is hydrogen, alkyl, cycloalkyl, phenyl or a 5- to 6-membered heterocyclic radical, it being possible for the organic radicals to carry substituents which are inert under the reaction conditions; R2 is alkyl, cycloalkyl, benzyl or C1-C3-alkenyl; R3 is hydrogen, alkyl or cycloalkyl and R4 is an aliphatic or cycloaliphatic radical or unsubstituted or substituted phenyl, or R4 together with R3is a 4- to 7-membered alkylene chain which can be interrupted by oxygen, sulfur or N-methyl, are prepared by selective amidation of an isoxazole-3,4-dicarboxylic diester of the formula II <IMAGE> II where R2 has the meanings of R2 and is identical to or different from R2.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9424095-A1
priorityDate 1992-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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