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Mendeleev Communications, 2021, Volume 31, Issue 2, Pages 210–212
DOI: https://doi.org/10.1016/j.mencom.2021.03.021
(Mi mendc881)
 

This article is cited in 13 scientific papers (total in 13 papers)

Communications

Renaissance of 4-(5-nitrofuran-2-yl)-5-arylamino substituted pyrimidines: microwave-assisted synthesis and antitubercular activity

E. V. Verbitskiyab, S. A. Baskakovaa, D. V. Belyaevac, D. V. Vakhrushevac, N. I. Eremeevac, G. L. Rusinovab, V. N. Charushinab

a I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
b Institute of Chemical Engineering, Ural Federal University, Ekaterinburg, Russian Federation
c Ural Research Institute for Phthisiopulmonology, Ekaterinburg, Russian Federation
Abstract: The Buchwald–Hartwig cross-coupling of 5-bromo-4-(furan-2-yl)pyrimidine with various anilines afforded the corresponding new 5-(arylamino)pyrimidines, the reaction being accelerated by microwave irradiation. Most of the obtained compounds proved to possess a high bacteriostatic in vitro effect against Mycobacterium tuberculosis H37Rv, Neisseria gonorrhoeae, and Staphylococcus aureus including Methicillin-resistant strain, which is stronger than that of the commercial drug Spectinomycin.
Keywords: pyrimidines, nitrofurans, anti-mycobacterial activity, Buchwald–Hartwig amination, cross-coupling reactions.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.3 Mb)


Citation: E. V. Verbitskiy, S. A. Baskakova, D. V. Belyaev, D. V. Vakhrusheva, N. I. Eremeeva, G. L. Rusinov, V. N. Charushin, “Renaissance of 4-(5-nitrofuran-2-yl)-5-arylamino substituted pyrimidines: microwave-assisted synthesis and antitubercular activity”, Mendeleev Commun., 31:2 (2021), 210–212
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  • This publication is cited in the following 13 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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