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Synthesis of chimeric amides of 2-arilaminopyrimidine series

https://doi.org/10.29235/1561-8331-2020-56-2-38-166-180

Abstract

Methodological approaches to the synthesis of 2-arylpyrimidine amides with predicted antitumor activity using the design of chimeric molecules by combining pharmacophore fragments of known antitumor drugs are considered. The results of the synthesis of chimeric amides containing, along with the 2-amino-pyrimidine fragment, fragments of other nitrogen and oxygen-containing heterocycles (piperazine, morpholine, isoxazole, etc.), aromatic cycles (benzene, methylnitroaniline, phenylenediamine) and functional (methyl-, amino-, carboxy-, etc.) groups in different positions of the molecule, are presented.

About the Author

Zh. V. Ignatovich
Institute of Chemistry of New Materials of the National Academy of Sciences of Belarus
Belarus

Zhanna V. Ignatovich – Ph. D. (Chemistry), Head of the Laboratory

36, F. Skorina Str., 220141, Minsk



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ISSN 1561-8331 (Print)
ISSN 2524-2342 (Online)