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Mendeleev Communications, 2021, Volume 31, Issue 1, Pages 42–45
DOI: https://doi.org/10.1016/j.mencom.2021.01.012
(Mi mendc828)
 

This article is cited in 16 scientific papers (total 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.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (4.4 Mb)


Citation: A. S. Kulikov, M. A. Epishina, E. S. Zhilin, A. D. Shuvaev, L. L. Fershtat, N. N. Makhova, “Design and synthesis of pyrazolo[3,4-d]pyridazine 5,6-dioxides as novel NO-donors”, Mendeleev Commun., 31:1 (2021), 42–45
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  • This publication is cited in the following 16 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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