Synthesis of new 3H-pyrrole derivatives from 3-aryl-2-oxa-7-azaspiro[4.4]nona-3,6,8-trienes


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Abstract

8-Amino-3-aryl-1-imino-4-methyl-6-(morpholin-4-yl)-2-oxa-7-azaspiro[4.4]nona-3,6,8-triene-9-carbonitriles reacted with acetic anhydride to give different products, depending on the solvent. The reaction in tetrahydrofuran gave the corresponding N-acyl derivatives at the imino group, whereas in pyridine 5-amino-2-morpholin-4-yl-3-(1-aryl-1-oxopropan-2-yl)-3H-pyrrole-3,4-dicarbonitriles were formed as a result of opening of the furan ring.

About the authors

M. Yu. Belikov

I.N. Ul’yanov Chuvash State University

Author for correspondence.
Email: belikovmil@mail.ru
Russian Federation, Moskovskii pr. 15, Cheboksary, 428015

I. V. Belikova

I.N. Ul’yanov Chuvash State University

Email: belikovmil@mail.ru
Russian Federation, Moskovskii pr. 15, Cheboksary, 428015

O. V. Ershov

I.N. Ul’yanov Chuvash State University

Email: belikovmil@mail.ru
Russian Federation, Moskovskii pr. 15, Cheboksary, 428015

S. V. Fedoseev

I.N. Ul’yanov Chuvash State University

Email: belikovmil@mail.ru
Russian Federation, Moskovskii pr. 15, Cheboksary, 428015

O. E. Nasakin

I.N. Ul’yanov Chuvash State University

Email: belikovmil@mail.ru
Russian Federation, Moskovskii pr. 15, Cheboksary, 428015

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