http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009256337-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-56
filingDate 2009-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_19f50c47b30b7f11992af6e6cd765286
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e9f1b45e6cc764c196a54601c63cea18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_09c25c87efa8118876c9dc04af426a7c
publicationDate 2009-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2009256337-A
titleOfInvention Process for producing piperidin-3-ylcarbamate compound
abstract A method for producing a piperidin-3-ylcarbamate compound is provided. In the presence of a palladium catalyst, the formula (1) (In the formula, R represents a benzyl group or an alkyl group having 1 to 8 carbon atoms.) Formula (2) in which a pyridin-3-ylcarbamate compound represented by formula (2) is brought into contact with hydrogen (In the formula, R represents the same meaning as described above.) The manufacturing method of the piperidin-3-yl carbamate compound shown by these. The obtained piperidin-3-ylcarbamate compound represented by the formula (2) can be optically resolved using optically active tartaric acid or optically active mandelic acid. [Selection figure] None
priorityDate 2008-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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