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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1d29f7ac2c7f9be9f7dae1a83bbb5c92
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-20
filingDate 1995-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a7c749a0f39f21276def72ab5a17fcc3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52fe74a969741a4c45d065b6a0c0de6b
publicationDate 1997-03-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0967354-A
titleOfInvention Process for producing thiazole acetic acid derivative containing protected hydroxyl group
abstract (57) Abstract: Under mild conditions, a compound having an amino group and a hydroxyl group in the same molecule is used as a raw material, and the amino group is left as it is, and a thiazole acetic acid derivative in which only the hydroxyl group is selectively protected is highly purified. Obtained in yield. A compound having an amino group and a hydroxyl group, such as ethyl 2- (2-amino-4-thiazolyl) -2-hydroxyiminoacetate, is treated with a halogenated aralkyl or a halogenated aralkyl in the presence of a strong base such as potassium t-butoxide. React with acid halide, for example triphenylmethyl chloride.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2011029596-A1
priorityDate 1995-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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