http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2413015-T3

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_981a37900e6991fb373304ed2ba5a703
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-38
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-38
filingDate 2005-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_246fff439e17661c0be8d156ab7ff9a5
publicationDate 2013-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2413015-T3
titleOfInvention Procedure for the preparation of substituted 2-alkoxycarbonyl-3-aminothiophenes
abstract Process for the preparation of 4-alkoxycarbonyl-3-aminothiophenes of general formula (I) ** Formula ** and / or its hydrochlorides of formula (I) '** Formula ** and / or its mono- or bis-acetylated form or mono- or bis-formylated of formulas (I) "** Formula ** in which R1 represents alkoxy with 1 to 6 carbon atoms optionally substituted with halogen or C1-C4 alkoxy, R2 represents alkyl with 1 to 6 carbon atoms optionally substituted with halogen or C1-C4 alkoxy or represents aryl or arylalkyl with respectively 6 or 10 carbon atoms in the aryl group and optionally 1 to 4 carbon atoms in the alkyl part respectively if applicable substituted with halogen, C1-C4 alkyl or C1-C4 alkoxy, and R3 represents an acyl or formyl substituent, characterized in that enamines of formula (II) are reacted ** Formula **
priorityDate 2004-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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