Synthesis of New Purine Derivatives Containing α- and ω-Amino Acid Fragments


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Abstract

New conjugates of purine and 2-aminopurine with several α- and ω-amino acids have been synthesized following two approaches based on the condensation and nucleophilic substitution reactions. The enantiomeric purity of the isolated compounds has been confirmed by reversed-phase HPLC using a chiral stationary phase to demonstrate the absence of racemization during the synthesis. The conjugates are inactive against Mycobacterium tuberculosis H37Rv.

About the authors

V. V. Musiyak

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
Russian Federation, Yekaterinburg

I. A. Nizova

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
Russian Federation, Yekaterinburg

T. V. Matveeva

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
Russian Federation, Yekaterinburg

G. L. Levit

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
Russian Federation, Yekaterinburg

V. P. Krasnov

Postovskii Institute of Organic Synthesis, Ural Branch

Author for correspondence.
Email: ca@ios.uran.ru
Russian Federation, Yekaterinburg

V. N. Charushin

Postovskii Institute of Organic Synthesis, Ural Branch

Email: ca@ios.uran.ru
Russian Federation, Yekaterinburg

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