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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C323-20
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-20
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filingDate 2002-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc27c1d05730c78c82f1fb4584cbb88e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ccd73e22b8ceb2c57be31a952d5ec640
publicationDate 2003-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20030086373-A
titleOfInvention Process for preparing thiazol derivative and the intermediate compounds for preparing the same
abstract The present invention is directed to 2- {2-methyl-4-[({4- Provided is a method for preparing methyl-2- [4- (trifluoromethyl) phenyl] -1,3-thiazol-5-yl} methyl) sulfanyl] phenoxy} acetic acid according to the following scheme.n n n n n n n n [Wherein, R 1 is an alkyl group having 1 to 4 carbon atoms, an alkyl or aralkylsilyl phenol protecting group, R 2 is a hydrogen atom and a methyl group, R 3 is a carboxylic acid protecting group having an alkyl group having 1 to 4 carbon atoms, X 1 Is a halogen atom, a hydrogen atom, X 2 is a halogen atom and a leaving group which is highly reactive to the electron affinity reaction, and M is lithium and magnesium ions.]n n n The present invention also provides the general formulas (III) and (VII), which are intermediates for the preparation of compound (X).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100753860-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101146784-B
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priorityDate 2002-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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