Synthesis of Substituted Aminopyrimidines as Novel Promising Tyrosine Kinase Inhibitors


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A procedure has been proposed for the synthesis of a series of substituted N-(1,3-thiazol-2-yl)-pyrimidin-2-amines and N-(pyrimidin-2-yl)thioureas by reactions of diethyl 2-(ethoxymethylidene)malonate and ethyl 2-(ethyoxymethylidene)-3-oxobutanoate with 1,3-thiazol-2-ylguanidines and amidinothiourea, respectively. Preliminary screening has revealed high inhibitory activity of ethyl 2-(carbamothioylamino)-4-methylpyrimidine-5-carboxylate and ethyl 2-(carbamothioylamino)-6-oxo-1,6-dihydropyrimidine-5-carbox-ylate toward several protein kinases.

作者简介

N. Stolpovskaya

Voronezh State University

编辑信件的主要联系方式.
Email: stolpovskaya@chem.vsu.ru
俄罗斯联邦, Voronezh

A. Kruzhilin

Voronezh State University

Email: stolpovskaya@chem.vsu.ru
俄罗斯联邦, Voronezh

A. Zorina

Voronezh State University

Email: stolpovskaya@chem.vsu.ru
俄罗斯联邦, Voronezh

Kh. Shikhaliev

Voronezh State University

Email: stolpovskaya@chem.vsu.ru
俄罗斯联邦, Voronezh

I. Ledeneva

Voronezh State University

Email: stolpovskaya@chem.vsu.ru
俄罗斯联邦, Voronezh

E. Kosheleva

Voronezh State University

Email: stolpovskaya@chem.vsu.ru
俄罗斯联邦, Voronezh

D. Vandyshev

Voronezh State University

Email: stolpovskaya@chem.vsu.ru
俄罗斯联邦, Voronezh

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