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
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
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.