http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PL-416802-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b49b25798cc9813e3f4a0fbe099b95ab
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D221-22
filingDate 2016-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4317b526075cec66304dc794a4886449
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bcc904fe53a98bbb015dd654ff2249d4
publicationDate 2017-01-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PL-416802-A1
titleOfInvention Chiral sulfinamides (1S, 4S, 5R) -2 - [(S) -1-phenylethyl] -4-amino-2-azabicyclo [3.2.1] octane derivatives and the method of obtaining them
abstract The subject of the application are chiral sulfinamides (1S, 4S, 5R) -2 - [(S) -1-phenylethyl] -4-amino-2-azabicyclo [3.2.1] octane derivatives which are used in asymmetric synthesis as chiral auxiliaries and organocatalysts and in the synthesis of compounds of biological importance. The method of obtaining sulfinamides of (1S, 4S, 5R) -2 - [(S) -1-phenylethyl] -4-amino-2-azabicyclo [3.2.1] octane derivatives of formula 1 consists in the reaction of at least one molar part ( 1S, 4S, 5R) -2 - [(S) -1-phenylethyl] -4-amino-2-azabicyclo [3.2.1] octane with at least one molar part of 4-methylphenylsulfonyl chloride in the presence of at least one molar part of triphenylphosphine and at least one molar part of a base selected from the group: KOH, Et3N, pyridine, wherein the reactions are carried out in a solvent in the temperature range 250 - 320 K.
priorityDate 2016-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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