Solvent-free reaction of 3-aryl-6-(3-nitrophenyl)-1,2,4-triazines with 4-(cyclohex-1-en-1-yl)morpholine


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Abstract

The aza-Diels–Alder reaction of 3-aryl-6-(3-nitrophenyl)-1,2,4-triazines with 4-(cyclohex-1-en-1-yl)morpholine as dienophile was accompanied by reduction of the nitro group to amino. In the reaction of 3-(4-methoxyphenyl)-6-(3-nitrophenyl)-1,2,4-triazine with 4-(cyclohex-1-en-1-yl)morpholine, 3-[3-(4-methoxyphenyl)-1,2,4-triazin-6-yl)aniline was formed together with the cycloaddition product.

About the authors

D. S. Kopchuk

Ural Federal University; Postovskii Institute of Organic Synthesis, Ural Branch

Email: gvzyryanov@gmail.com
Russian Federation, ul. Mira 19, Yekaterinburg, 620002; ul. S. Kovalevskoi/Akademicheskaya 22/20, Yekaterinburg, 620990

A. F. Khasanov

Ural Federal University

Email: gvzyryanov@gmail.com
Russian Federation, ul. Mira 19, Yekaterinburg, 620002

A. P. Krinochkin

Ural Federal University

Email: gvzyryanov@gmail.com
Russian Federation, ul. Mira 19, Yekaterinburg, 620002

I. S. Kovalev

Ural Federal University

Email: gvzyryanov@gmail.com
Russian Federation, ul. Mira 19, Yekaterinburg, 620002

G. V. Zyryanov

Ural Federal University; Postovskii Institute of Organic Synthesis, Ural Branch

Author for correspondence.
Email: gvzyryanov@gmail.com
Russian Federation, ul. Mira 19, Yekaterinburg, 620002; ul. S. Kovalevskoi/Akademicheskaya 22/20, Yekaterinburg, 620990

V. L. Rusinov

Ural Federal University; Postovskii Institute of Organic Synthesis, Ural Branch

Email: gvzyryanov@gmail.com
Russian Federation, ul. Mira 19, Yekaterinburg, 620002; ul. S. Kovalevskoi/Akademicheskaya 22/20, Yekaterinburg, 620990

O. N. Chupakhin

Ural Federal University; Postovskii Institute of Organic Synthesis, Ural Branch

Email: gvzyryanov@gmail.com
Russian Federation, ul. Mira 19, Yekaterinburg, 620002; ul. S. Kovalevskoi/Akademicheskaya 22/20, Yekaterinburg, 620990

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