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Heteroarylation of acetonitriles. 3. Heteroarylation of pyridin-2-yl and quinolin-2-ylacetonitriles by chloroquinoxalines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

It has been shown that α-chloroquinoxalines heteroarylate pyridin-2-yl and quinolin2-ylacetonitriles primarily at the methylene group. A method has been developed for synthesizing 1-R-2-amino-3-heteroarylpyrrolo[2,3-b]quinoxalines permitting the preparation of compounds containing the pyridine and quinoline nuclei.

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For Communication 2, see [1].

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 85–87, January, 1990.

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Kozynchenko, A.P., Volovenko, Y.M., Babichev, F.S. et al. Heteroarylation of acetonitriles. 3. Heteroarylation of pyridin-2-yl and quinolin-2-ylacetonitriles by chloroquinoxalines. Chem Heterocycl Compd 26, 73–75 (1990). https://doi.org/10.1007/BF00506853

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  • DOI: https://doi.org/10.1007/BF00506853

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