http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2000355592-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D205-04
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filingDate 1999-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_26ddddbdef0bdb8f3f5b981eb2143b8a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8ab3b7e4079b3855301d0667620af5f3
publicationDate 2000-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2000355592-A
titleOfInvention Method for producing 3-mercapto-1- (1,3-thiazolin-2-yl) azetidine
abstract PROBLEM TO BE SOLVED: To provide a simple industrially applicable 3-mercapto-1- (1,3-thiazolin-2-yl) azetidine used as a side chain at the 2-position of a carbapenem antibiotic. Providing a unique manufacturing method. SOLUTION: The following formula (II): (In the formula, Bzl represents a benzyl group.) Benzyl-3-hydroxyazetidine is used as a starting compound, which is reacted with a sulfonic acid halide derivative in the presence of a base, the benzyl group of the obtained compound is removed, reaction with sodium thiosulfate, 2-alkylthio-1,2 The compound obtained through a reaction with a 3-thiazoline derivative is further treated with an acid or with a thiol compound. A method for producing 3-mercapto-1- (1,3-thiazolin-2-yl) azetidine represented by the formula:
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100441406-B1
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type http://data.epo.org/linked-data/def/patent/Publication

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