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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2021 Volume 31, Issue 1, Pages 42–45 (Mi mendc828)

This article is cited in 16 papers

Communications

Design and synthesis of pyrazolo[3,4-d]pyridazine 5,6-dioxides as novel NO-donors

A. S. Kulikova, M. A. Epishinaa, E. S. Zhilina, A. D. Shuvaevab, L. L. Fershtata, N. N. Makhovaa

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation

Abstract: A simple and effective protocol for the synthesis of 2H-pyrazolo[3,4-d]pyridazine 5,6-dioxides includes a transformation of accessible 3,4-diacetyl-5-methyl-1H-pyrazoles into the corresponding 1,4-dioximes followed by their N2O4- mediated oxidative cyclization. All transformations proceed under mild conditions in good to high yields. According to the Griess assay, synthesized 2H-pyrazolo[3,4-d]pyridazine 5,6-dioxides showed promising NO-donor profiles producing NO in a wide range of concentrations.

Keywords: NO-donors, oxidative cyclization, pharmacologically oriented compounds, 1,2,5-oxadiazoles, pyrazolo[3,4-d]pyridazine 5,6-dioxides, dinitrogen tetraoxide.

Language: English

DOI: 10.1016/j.mencom.2021.01.012



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