Synthesis of β-Dimethylaminoethyl and α-Hydroxy-β-Dimethylaminoethyl Derivatives from Organolithium Compounds and Tetramethyoxamide
- 1 January 1973
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 3 (5) , 325-332
- https://doi.org/10.1080/00397917308063484
Abstract
The important biological activity of a variety of aromatic and heterocyclic systems having β-dimethylaminoethyl side chains and their α-hydroxy analogs (c.f. bufotenin, N-methylepinephrine, etc.) has focused the attention of the organic chemist on methods of introducing these functions, and a variety of approaches have been developed. A convenient synthesis has recently been reported3, which utilizes the α-hydroxy-β-dimethylaminoethyl function as an intermediate in the preparation of β-dimethylaminoethyl derivatives, thus providing either or both of these pharmacophoric groups.Keywords
This publication has 6 references indexed in Scilit:
- Benzo[b] thiophene derivatives. XIX. The sulfur isosteres of psiloein and related isomersJournal of Heterocyclic Chemistry, 1973
- Synthesis of 1,4 and 1,5 diketones from N,N,N1,N1-tetramethyl diamides and organolithium reagentsThe Journal of Organic Chemistry, 1973
- HANDBOOK OF CHEMISTRY AND PHYSICS, 49th edThe Lancet Healthy Longevity, 1969
- Benzo[b]thiophene derivatives. XII. Synthesis of some 3-benzo[b]thienylalkylamines and comparison of their central nervous system activity with tryptamine isosteresJournal of Medicinal Chemistry, 1968
- Dimethylamides from Alkali Carboxylates and Dimethylcarbamoyl ChlorideThe Journal of Organic Chemistry, 1963
- Substances curarisantes dérivées de la cholineBulletin des Sociétés Chimiques Belges, 1952