New chemical transformation of substituted dinitroacetonitrile in the reaction with isoquinoline in presence of dimethylbut-2-indioate

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The reaction of substituted dinitroacetonitrile with isoquinoline in the presence of dimethylbut-2-indioate results in the formation of 1,3-dipolar cycloaddition products – a mixture of diastereomeric dimethyl-2-dinitromethyl-1,1bH-pyrimido[2,1-a]isoquinoline-3,4-dicarboxylates. The obtained compounds can be considered as promising synthons with potential antituberculosis and fungicidal activity.

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作者简介

A. Tyrkov

Astrakhan Tatishchev State University

编辑信件的主要联系方式.
Email: tyrkov@rambler.ru
俄罗斯联邦, pl. Shaumyana, 1, Astrakhan, 414000

Е. Yurtaeva

Pyatigorsk Medical and Pharmaceutical Institute – branch of Volgograd State Medical University

Email: tyrkov@rambler.ru
俄罗斯联邦, prosp. Kalinina, 11, Pyatigorsk, 357532

参考

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2. Scheme

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3. Figure. Diastereoisomeric forms of compounds 4a–e R = NO2 (a), CO2Et (b), CO2Me (c), Cl (d), F (e)

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4. Figure

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