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  • Copper-catalyzed [5+1] annulation of 2-ethynylanilines with an N,O-acetal leading to construction of quinoline derivatives.

Copper-catalyzed [5+1] annulation of 2-ethynylanilines with an N,O-acetal leading to construction of quinoline derivatives.

Organic letters (2012-01-27)
Norio Sakai, Kosuke Tamura, Kazuyori Shimamura, Reiko Ikeda, Takeo Konakahara
ABSTRACT

A novel copper-catalyzed [5 + 1] annulation of 2-ethynylanilines with an N,O-acetal, which functioned as a C1 part, leading to the preparation of quinoline derivatives with an ester substituent on the 2-position is described. A combination of CuBr(2) and trifluoroacetic acid (TFA) promoting [5 + 1] annulation of the 2-ethynylaniline with ethyl glyoxylate is also demonstrated.

MATERIALS
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Product Description

Sigma-Aldrich
Glyoxylic acid solution, 50 wt. % in H2O