Abstract
A revisited synthesis of 2-aryl-6-methyl-1,2-dihydro-1H-pyridin-4-ones and their saturated analogues 2-aryl-6-methylpiperidin-4-ols is described. A five steps procedure, using the sulfinimine chemistry, to prepare a key intermediate β-(6-chloronicotinic)-β-amino ester is also reported. In vivo spontaneous working memory activity of these compounds has been investigated in the mouse. Results obtained with 2-(3-chlorophenyl)-6-methyl-1,2-dihydro-1H-pyridin-4-one 9b, the most effective derivative in this model, have been reported. © 2005 Taylor & Francis.
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Leflemme, N., Freret, T., Boulouard, M., Dallemagne, P., & Rault, S. (2005). Synthesis and preliminary in vivo evaluation of new 2-Aryl-6-methyl-1,2-dihydro-1H-pyridin-4-ones and 2-Aryl-6-methylpiperidin-4-ols, as potential anti-amnesiant agents. Journal of Enzyme Inhibition and Medicinal Chemistry, 20(6), 551–556. https://doi.org/10.1080/14756360500212266
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