Psilocin analogs II. Synthesis of 3‐[2‐(dialkylamino)ethyl]‐, 3‐[2‐(N‐methyl‐N‐alkylamino)ethyl]‐, and 3‐[2‐(cycloalkylamino)ethyl]indol‐4‐ols
Document Type
Article
Publication Date
1-1-1981
Department
Department of Chemistry; Department of Chemical Engineering
Abstract
Structural alteration of the Nb‐substituents of psilocin (3‐[2‐dimethylamino)ethyl]indol‐4‐ol) (12a) has led to a number of compounds containing known pharmacophoric groups. Further, it is hoped that the subtle changes in the nature of these substituents may lead to a clearer understanding of the structure‐activity relationships of the 4‐hydroxytryptamine hallucinogens.
Publication Title
Journal of Heterocyclic Chemistry
Recommended Citation
Repke, D.,
Ferguson, W.,
&
Bates, D.
(1981).
Psilocin analogs II. Synthesis of 3‐[2‐(dialkylamino)ethyl]‐, 3‐[2‐(N‐methyl‐N‐alkylamino)ethyl]‐, and 3‐[2‐(cycloalkylamino)ethyl]indol‐4‐ols.
Journal of Heterocyclic Chemistry,
18(1), 175-179.
http://doi.org/10.1002/jhet.5570180131
Retrieved from: https://digitalcommons.mtu.edu/michigantech-p/3744
Publisher's Statement
Copyright © 1981 Journal of Heterocyclic Chemistry. Publisher’s version of record: https://doi.org/10.1002/jhet.5570180131