Abstract
Condensing substituted l-aryl-5-hydroxyindoles with bisdimethylaminomethane, or sodium-alcohol reduction of l-aryl-2-methyl-3-acetyl-5-methoxyindoles gives 4-dimethylaminomethyl and 3-alkylamino derivatives of 1-aryl-5-hydroxy (methoxy) indole, isolated as the hydrochlorides.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
References
U. S. Patent no. 2 852 527, 1959; C. A., 53, 816, 1959.
A. N. Grinev, N. K. Kul'bovskaya, and A. P. Terent'ev, ZhOKh, 25, 1355, 1955.
A. N. Grinev, V. N. Ermakova, and A. P. Terent'ev, DAN, 121, 862, 1958.
A. N. Grinev, Hun Shih-chün, and A. P. Terent'ev, ZhOKh, 31, 1902, 1961.
A. N. Grinev and N. V. Venevtseva, ZhOKh, 33, 820, 1963.
A. N. Grinev, V. I. Shvedov, and E. K. Panisheva, ZhOrKh, 1, 2051, 1965.
A. N. Grinev, V. I. Shvedov, and I. P. Sugrobova, ZhOKh, 31, 2298, 1961.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Grinev, A.N., Shvedov, V.I. & Panisheva, E.K. Synthesis of alkylamine derivatives of 1-aryl-5-hydroxyindole. Chem Heterocycl Compd 2, 287–288 (1967). https://doi.org/10.1007/BF00742369
Issue Date:
DOI: https://doi.org/10.1007/BF00742369