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Total synthesis of sufentanil

Authors
Shin, DYRyu, JSHyun, SSPark, HJJeon, ROSuh, YG
Issue Date
Aug-1999
Publisher
PHARMACEUTICAL SOC KOREA
Keywords
total synthesis; sufentanil; analgesics; piperidine; oxirane
Citation
ARCHIVES OF PHARMACAL RESEARCH, v.22, no.4, pp 398 - 400
Pages
3
Journal Title
ARCHIVES OF PHARMACAL RESEARCH
Volume
22
Number
4
Start Page
398
End Page
400
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/150171
DOI
10.1007/BF02979064
ISSN
0253-6269
1976-3786
Abstract
Sufentanil, a potent anilidopiperidine analgesic, was synthesized from a simple thiophenylethylamine via six step sequence. The key parts of this synthesis involved an efficient construction of thiophenylethylpiperidone by aminomethano desilylation-cyclization followed by Swern oxidation and a direct regioselective N-nucleophilic spiral epoxide cleavage with aniline promoted by Lewis acids.
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