http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2016102261-A4

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_317f207d800e7d0d06f670d94cc9c126
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-35
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-00
filingDate 2016-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4a18cc5cc94a7dbef071858a27623e8d
publicationDate 2017-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AU-2016102261-A4
titleOfInvention Pyrimethamine drug intermediates chloro benzonitrile synthesis method
abstract Pyrimethamine drug intermediates chloro benzonitrile synthesis method , comprising the following steps: equipped with a stirrer, a thermometer, a reflux condenser and a dropping funnel, the reaction vessel was added 1.3mol p-chlorobenzyl (2), 0.56 mol stannous chloride, controlling the stirring speed 130-160rpm, elevated solution temperature to 90-95 C, slowly added 1.5-1.7mol cyanamide (3), controlled dropping time in 1-2 h, continued the stirring 4-5h, reducing the temperature of the solution to 10 - 15 C, adding 230ml sodium chloride solution, separated the water layer, the oil layer was washed with brine solution, washed with acetonitrile solution, vacuum distillation, fraction is recrystallized from ethyl acetate solution, got chloro benzonitrile .
priorityDate 2015-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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