SYNTHESIS OF PSILOCIN LABELED WITH C-14 AND H-3

被引:6
作者
POON, G [1 ]
CHUI, YC [1 ]
LAW, FCP [1 ]
机构
[1] SIMON FRASER UNIV, DEPT BIOL SCI, ENVIRONM TOXICOL PROGRAM, BURNABY V5A 1S6, BC, CANADA
关键词
D O I
10.1002/jlcr.2580230207
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
14C- and 3H-labelled psilocin (4-hydroxy-N,N-dimethyl-tryptamine), the principal, active agent of hallucinogenic mushrooms, was synthesized from 2-methyl-3-nitrophenol via 4-benzyloxyindole. 14C-Labelled potassium cyanide was reacted with 4-benzyloxygramine (obtained from 4-benzyloxyindole) to give 14C-4-benzyloxy-3-indole acetic acid, an intermediate for 14C-psilocin synthesis. 3H-Labelled lithium aluminium hydride was used to react with 4-benzyloxy-3-indole-N,N-dimethyl-glyoxylamide (obtained from 4-benzyloxyindole) to give 3H-4-benzyloxy-psilocin which was debenzylated to form 3H-psilocin.
引用
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页码:167 / 174
页数:8
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