Abstract:Modification of biologically active cycloalkaneindoles by incorporation of a 2-trifluoromethylimidazo[1,2-а]pyridin-6-yl fragment has been proposed and performed via the interaction with 3-fluoro-2trifluoromethylimidazo[1,2-а]pyridines in the presence of potassium hydroxide. The action of the prepared compounds on neuronal NMDA receptors has been studied by means of radioligand binding.
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