http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2284999-C1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-68
filingDate 2005-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_57f3eacdf9aa28fe433e8af7c5b7110c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_36e287ad20071ca751d18b44af91a073
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publicationDate 2006-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2284999-C1
titleOfInvention Method for preparing 2-cyano-6-methoxybenzthiazole
abstract FIELD: organic chemistry, chemical technology. n SUBSTANCE: invention relates to the improved method for synthesis of 2-cyano-6-methoxybenthiazole that is a key intermediate compound used in synthesis of luminescent biological systems, in particular, lupiferin. Method involves cyaniding reaction of 2-chloro-6-methoxybenzthiazole wherein acetonecyanohydrine is used as a cyaniding agent that is treated with alkaline metal alcoholate alcoholic solution, benzene is added and azeotropic mixture alcohol-benzene is distilled off followed by addition of dimethylsulfoxide and 2-chloro-6-methoxybenzthiazole. Method allows avoiding contact of workers with highly toxic cyanides and to obtain 2-cyano-6-methoxybenzthiazole with higher yield 50-50.8% as compared with the prototype (40%). n EFFECT: improved method of synthesis. n 3 ex
priorityDate 2005-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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