Solvent-Free reaction of 3,6-Diaryl-1,2,4-Triazine-5-Carbonitriles with 2-Amino-4-aryloxazoles

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Solvent-free reaction of 3,6-diaryl-1,2,4-triazine-5-carbonitriles with 2-amino-4-aryloxazoles was studied. In this case, the formation of 3- and 4-aryl-substituted pyridines (two isomeric products) in yields up to 20 and 27%, respectively, was found. This result is different from that for the reaction of 3-(2-pyridyl)-1,2,4-triazine-5-carbonitriles with these substrates. Thus, in this case, 2-amino-4-aryloxazoles act as synthetic analogues of arylacetylenes.

作者简介

A. Rammohan

Ural Federal University

Email: gvzyryanov@gmail.com

Ya. Shtaitz

Ural Federal University

Email: gvzyryanov@gmail.com

E. Ladin

Ural Federal University

Email: gvzyryanov@gmail.com

A. Krinochkin

Ural Federal University;I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences

Email: gvzyryanov@gmail.com

P. Slepukhin

Ural Federal University;I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences

Email: gvzyryanov@gmail.com

V. Sharutin

South Ural State University

Email: gvzyryanov@gmail.com

E. Sharafieva

Ural Federal University;Ural State Medical University of the Ministry of Health of Russia

Email: gvzyryanov@gmail.com

T. Pospelova

Ural Federal University

Email: gvzyryanov@gmail.com

D. Kopchuk

Ural Federal University;I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences

Email: gvzyryanov@gmail.com

G. Zyryanov

Ural Federal University;I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences

Email: gvzyryanov@gmail.com

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