http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107033010-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_67068c0d95f977412b821eb313b7f70f
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C213-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F3-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-70
filingDate 2017-05-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd631260fb96ea5293bab347508f70d4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ab2a9a53935f7b76c9af63e636a9edab
publicationDate 2017-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-107033010-A
titleOfInvention A kind of method of asymmetric syntheses anti-AIDS drug efavirenz key intermediate
abstract The invention discloses a kind of method of asymmetric syntheses anti-AIDS drug efavirenz key intermediate, belong to medical synthesis technical field.Including 2 methyltetrahydrofurans, alkaline reagent, alcohol compound, chiral aminoalcohol solution, cyclopropyl acethlene are reacted, after add the amino trifluoro-benzene ketone of 5 chlorine 2 occur addition reaction, again by terminating reaction liquid terminating reaction, the chlorine a cyclopropyl acethlene a trifluoromethyl benzyl alcohols of key intermediate (S) 2 amino 5 of efavirenz are obtained.Avoiding needs the operating process of the lithium salts, sodium salt or its RMgBr that first prepare cyclopropyl acethlene in industrial production, significantly reduce the operation difficulty and cost of reaction, is adapted to industrialized production.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113880693-B
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priorityDate 2017-05-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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