http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7345188-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_07addebfc9446dc5a9a77692ebf4dac1
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C319-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C315-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C319-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C317-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C317-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C315-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C315-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-00
filingDate 2004-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d0c04a9c1985eab4709b541cc677974a
publicationDate 2008-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7345188-B2
titleOfInvention Process for preparing benzhydrylthioacetamide
abstract The present invention is directed to an improved process for preparing modafinil wherein benzhydrylthioacetate is prepared in high yield and purity by the reaction of a haloacetate with the reaction product of thiourea and benzhydrol. The reaction employing the haloacetate is conducted in a solvent comprising an organic solvent such as methanol having dissolved therein an organic base or an inorganic basic salt such as sodium bicarbonate. The resulting benzhydrylthioacetate can be amidated and then oxidized to provide the pharmaceutical grade modafinil in high yield and purity.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2008319227-A1
priorityDate 2003-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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