http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2020213714-A1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B53-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-42
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filingDate 2020-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_64ae17edc4c65cdc4e9e7e8cf682833e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e6ad4a9e7f1b01295a9d65ab21a89bcf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c2169769dbb899ff646c5268ab261be8
publicationDate 2020-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2020213714-A1
titleOfInvention Method for producing cis-(-)-fluocino piperidol
abstract The present invention provides a method in which when using (+)-dibenzoyl-D-tartaric acid to optically divide (±)-1-methyl-4-(2,4,6-trimethoxyphenyl)-3-piperidinone, an ether-based solvent is added and an extremely high yield of (R)-1-methyl-4-(2,4,6-trimethoxyphenyl)-3-piperidinone (+)-dibenzoyl-D-tartrate is thereby obtained, a slurry thereof is treated with a base, a "three-dimensionally bulky reducing agent" is subsequently used, and cis-(-)-fluocino piperidol is thereby produced with surprisingly high selectivity.
priorityDate 2019-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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