http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5679667-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a2fb784feb0deee31fdf1cd0665485b8
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-14
filingDate 1979-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b50adb15bcb69ba3c37be6bfced02292
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6092e96e3cbeee49d30a34dc3d7f6d11
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publicationDate 1981-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5679667-A
titleOfInvention Preparation of erythro 2- 4-benzylpiperidino -1- 4- hydroxyphenyl propanol
abstract PURPOSE: To obtain the titled compound simply and in high yield, by reducing 4'- benzyloxy-2(4-benzylpiperidino)propiophenone in the form of a salt or in the presence of an acidic substance with sodium boron hydride, followed by debenzylation. n CONSTITUTION: 4'-Benxyloxy-2-(4-benzylipiperidino)propiophenone shown by the formula II is reduced with sodium boron hydride in the state of a salt of the compound or in the presence of an acidic substance (e.g., hydrochloric acid, acetic acid, etc.), to give an alcohol derivative shown by the formula II, which is debenzylated to give erythro 2-(4-benzylpiperidiono)-1-(4-hydroxyphenyl)propanol shown by the formula I. The reduction with sodium boron hydride in the state of a salt of the propiophenone shown by the formula III or in the presence of the acidic substance provids the erythro derivatice shown by the formula II in high selectivity. n USE: An improving agent for cerebrovascular stream and remedy for sequela of cerabral infract. n COPYRIGHT: (C)1981,JPO&Japio
priorityDate 1979-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 21.