Synthesis of acetylcholinesterase inhibitors on the basis of 9-isothiocyanato-1,2,3,4-tetrahydroacridine: 2-[1,2,3,4-tetrahydroacridin-9-yl)imino]-3-substituted 1,3-thiazolidin-4-ones

Citation
P. Kristian et al., Synthesis of acetylcholinesterase inhibitors on the basis of 9-isothiocyanato-1,2,3,4-tetrahydroacridine: 2-[1,2,3,4-tetrahydroacridin-9-yl)imino]-3-substituted 1,3-thiazolidin-4-ones, HETEROCYCLE, 49, 1998, pp. 197-204
Citations number
10
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
HETEROCYCLES
ISSN journal
03855414 → ACNP
Volume
49
Year of publication
1998
Pages
197 - 204
Database
ISI
SICI code
0385-5414(199812)49:<197:SOAIOT>2.0.ZU;2-H
Abstract
The synthesis of 2-[(1,2,3,4-tetrahydroacridin-9-yl)imino]-3-substituted 1, 3-thiazolidin-4-ones (5a-e) via cyclization of N-(1,2,3,4-tetrahydroacridin -9-yl)-S-methoxycarbonylmethyl-N'-substituted isothiourea hydrobromides was elaborated. As a synthon, 9-isothiocyanato-1,2,3,4-tetrahydroacridine, an analogue of tacrine, was used. The reaction represents a simple way for the preparation of new cholinergic compounds.