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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D281-16
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D281-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-554
filingDate 2003-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_628b4ef5d96385e6fa1adc454efe59c7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f2e75662177fc56a91a5a9415b6b8f81
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_848ed3c885da32c946332eaa52297fdf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ab76de393e49dd009f2e8173522c147
publicationDate 2007-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2007066589-A1
titleOfInvention Method of preparing 10th-dibenzo[b,f][11,4]thiazepin-11-one
abstract Disclosed is a method of preparing 10H-dibenzo[b,f][1,4]thiazepin-11-one, including reacting dithiosalicylic acid with 1-chloro-2-nitrobenzene in a basic aqueous solution in the presence or absence of a reducing agent, to prepare 2-(2-nitrophenylsulfuryl)benzoic acid; subjecting the 2-(2-nitrophenylsulfuryl)benzoic acid to nitro group reduction in the presence of hydrogen, a solvent and a heterogeneous metal catalyst, to prepare 2-(2-aminophenylsulfuryl)benzoic acid; and directly cyclizing the 2-(2-aminophenylsulfuryl)benzoic acid in an organic solvent in the presence or absence of an acid catalyst. The method according to the present invention is economical due to the use of the inexpensive starting material, and also environmentally friendly and efficient by minimizing the use of the organic solvent and performing direct cyclization without the activation of carboxylic acid.
priorityDate 2002-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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