http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2005010002-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4745
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 2004-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_80462ed4515bb1b382798f715c8c0660
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_506d5ccda3a0508139cba8f9ba4c920f
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publicationDate 2005-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2005010002-A1
titleOfInvention Process for the synthesis of zolpidem
abstract The present invention relates to processes for the preparation of zolpidem of Formula V as shown in the accompanying drawings or pharmaceutically acceptable salts thereof from N, N-dimethyl-3-(4-methyl) benzoyl propionamide of Formula II. The process includes (a) reacting N,N-dimethyl-3-(4-methyl) benzoyl propionamide of Formula II with bromine to get the bromo amide of Formula III; (b) condensing the bromo amide of Formula III with 2-amino-5-methylpyridine of Formula IV to get the zolpidem base of Formula V; and (c) converting zolpidem base of Formula V to its hemitartarate salt of Formula VII.
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priorityDate 2003-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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