http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7772406-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d24321bed2edef57b40e064ce34f0a6e
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D207-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-40
filingDate 2006-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2010-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dbb1dd57a44e3bcbd8894492ef43c2a9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa8ebb581d3899424f11f44cb2f62026
publicationDate 2010-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7772406-B2
titleOfInvention Process for production of benzyloxypyrrolidine derivative, and process for production of hydrochloride salt powder of optically active benzyloxypyrrolidine derivative
abstract Provided are: a process for production of a benzyloxypyrrolidine derivative in high yield and safety, and a process for production of a hydrochloride powder of a benzyloxypyrrolidine derivative in high yield and safety; the process for production of a benzyloxypyrrolidine derivative expressed by the general formula (2) [Chemical formula 2], in reacting a pyrrolidinol derivative represented by the general formula (1) [Chemical formula 1] with a benzyl halide derivative in the presence of an alkali metal hydroxide, wherein the reaction is carried out in either of the following conditions A or B; condition A: an aprotic polar solvent, and condition B: an aliphatic ether solvent containing a phase transfer catalyst:
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priorityDate 2005-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 388.