http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007032647-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D223-28
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D223-18
filingDate 2004-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_489f776446d234d02e65cfeb357eb83d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d6210f91359c2d3abefa9e3dc1ff8dc
publicationDate 2007-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2007032647-A1
titleOfInvention Novel process for preparation of 10-oxo-10, 11-dihydro-5h-dibenz [b,f] azepine-5-carbox- amide (oxcarbazepine) via intermediate, 10-methoxy-5h-debenz[b,f] azepine-5-carbonyl- chloride
abstract A process for preparation of 10-oxo-10,11-dihydro-5H-dibenz[b,f]azepine-5-carboxamide (oxcarbazepine) via intermediate 10-methoxy-5H-dibenz[b,f]azepine-5-carbonyl chloride, comprising the steps: a) Preparation of an intermediate 10-methoxy-5H-dibenz[b,f]azepine-5 carbonyl, chloride from 10-methoxyiminostillbene using bis (trichloromethyl) carbonate (BTC) with organic base such as aliphatic or aromatic tertiary amines in organic solvent; b) Conversion of the intermediate to 10-methoxy-5H-dibenz[b,f]azepine-5-carboxamide using ammonia in organic solvent; c) Formation of oxcarbazepine from step (b) using Bronsted acid in an organic solvent at a temperature between 25° C.-80° C., preferably at 50° C. to 70° C.; and d) Isolation of oxcarbazepine.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2011065917-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007254033-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7858779-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007149507-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8530647-B2
priorityDate 2004-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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