Leflemme_2005_J.Enzyme.Inhib.Med.Chem_20_551

Reference

Title : 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 - Leflemme_2005_J.Enzyme.Inhib.Med.Chem_20_551
Author(s) : Leflemme N , Freret T , Boulouard M , Dallemagne P , Rault S
Ref : J Enzyme Inhib Med Chem , 20 :551 , 2005
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 beta-(6-chloronicotinic)-beta-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.

PubMedSearch : Leflemme_2005_J.Enzyme.Inhib.Med.Chem_20_551
PubMedID: 16408790

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Citations formats

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
J Enzyme Inhib Med Chem 20 :551

Leflemme N, Freret T, Boulouard M, Dallemagne P, Rault S (2005)
J Enzyme Inhib Med Chem 20 :551