http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PT-88504-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_05a203d85ee01909eaf728dc16f0f6cb
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D513-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D513-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-06
filingDate 1988-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8101e46de1b76a9b6281859d68f71a6c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_02f1f4f9d4d095893f388b69c4bbc5f4
publicationDate 1992-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PT-88504-B
titleOfInvention PROCESS FOR THE PREPARATION OF HALOALQUIL-TIAZOLES
abstract A process for the preparation of a compound of the formula <CHEM> wherein R<1> 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 <CHEM> wherein A is as defined above or a hydrohalide salt thereof. 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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