Organometal-Free Arylation and Arylation/Trifluoroacetylation of Quinolines by Their Reaction with CF<sub>3</sub>-ynones and Base-Induced Rearrangement
Vasiliy M. Muzalevskiy, Kseniya V. Belyaeva, Б. А. Трофимов, Valentine G. Nenajdenko
Abstract
-ynones resulted in the formation of 1,3-oxazinoquinolines. Subsequent treatment of the reaction mixture with a base initiated deep structural transformation of primary products. Both steps proceed in very high yield. As a result, unusual rearrangement of 1,3-oxazinoquinolines to form either 2-arylquinolines or 2-aryl-3-trifluoroacetylquinolines was discovered. The decisive role of the base in the reaction direction was shown. Using these reactions, highly efficient pathways to 2-arylquinolines and 2-aryl-3-trifluoroacetylquinolines were elaborated to provide the corresponding compounds in high yields using a simple one-pot procedure. The possible mechanism of rearrangement is discussed.