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Mendeleev Communications, 2022, Volume 32, Issue 3, Pages 393–394
DOI: https://doi.org/10.1016/j.mencom.2022.05.034
(Mi mendc675)
 

This article is cited in 1 scientific paper (total in 1 paper)

Communications

Synthesis of new heterocyclic systems fused at pyrazolo[3,4-c]-2,7-naphthyridine core

S. N. Sirakanyana, E. K. Hakobyana, D. Spinellib, A. Geronikakic, V. G. Kartsevd, H. A. Yegoryana, A. A. Hovakimyana

a Scientific Technological Center of Organic and Pharmaceutical Chemistry, National Academy of Sciences of the Republic of Armenia, Yerevan, Armenia
b Dipartimento di Chimica ''G. Ciamician'', Universita degli Studi di Bologna, Bologna, Italy
c Department of Chemical Engineering, Aristotle University of Thessaloniki, Thessaloniki, Greece
d 'InterBioScreen Ltd.', Chernogolovka, Moscow Region, Russian Federation
Abstract: Efficient syntheses of new heterocyclic systems comprising pyrimido[1',2':1,5]pyrazolo[3,4-c]-2,7-naphthyridine, pyrazolo[3,4-c][1,2,4]triazolo[3,4-a]-2,7-naphthyridine and pyrazolo[3,4-c]tetrazolo[5,1-a]-2,7-naphthyridine cores were performed in two simple steps. In the first step, pyrazole ring was fused at the 2-chloro-3-cyanopyridine moiety by treatment with hydrazine. In the second step, pyrimidine part was fused at the thus formed 3-aminopyrazole moiety by heterocyclization with acetylacetone.
Keywords: 2,7-naphthyridines, pyrimido[1' 2':1,5]pyrazolo[3,4-c]-2,7-naphthyridine, pyrazolo[3,4-c][1,2,4]triazolo[3,4-a]-2,7- naphthyridines, pyrazolo[3,4-c]tetrazolo[5,1-a]-2,7-naphthyridine, heterocyclization, hydrazine, acetylacetone.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (8.8 Mb)


Citation: S. N. Sirakanyan, E. K. Hakobyan, D. Spinelli, A. Geronikaki, V. G. Kartsev, H. A. Yegoryan, A. A. Hovakimyan, “Synthesis of new heterocyclic systems fused at pyrazolo[3,4-c]-2,7-naphthyridine core”, Mendeleev Commun., 32:3 (2022), 393–394
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  • This publication is cited in the following 1 articles:
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