http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-198701-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D513-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-64
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D513-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-64
filingDate 1988-09-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_23f90f494a78f4dbd00650de98d5e7d6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cbd86f93b01ec295f80105a0d32d69cc
publicationDate 1989-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-198701-B
titleOfInvention New process for producing halogeno-alkyl-thiazols condenzed with rings of benzene or pyridine
abstract A process for the preparation of a compound of the formulan wherein R¹ is hydrogen or (C₁-C₄)alkyl, X is chloro or bromo and A represents a 6 membered carbocylic aromatic or a 5 or 6 membered heterocyclic ring which is optionally substituted by one of iodo or trifluoro­methylthio, or one or two of fluoro, chloro, bromo, (C₁-C₄)alkyl, (C₁-C₄)alkoxy, (C₁-C₄)alkylthio, (C₁-C₄)alkylsulfinyl, (C₁-C₄)alkylsulfonyl, or trifluoromethyl, comprising reacting haloacetonitrile with a compound of the formula wherein A is as defined above or a hydrohalide salt thereof. n The compounds of the formula (I) are useful intermediates in the preparation of heterocyclic oxophthalazinyl acetic acids having aldose reductase inhibitory activity. Some of the compounds of the formula (I) are novel, and these also form a part of the invention.
priorityDate 1987-09-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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