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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2019, том 29, выпуск 6, страницы 658–660 (Mi mendc1621)

Эта публикация цитируется в 2 статьях

Communications

Acetylene based short route from 2,2,6,6-tetramethylpiperidin-4-one oxime to 2-(pyrazol-5-yl)-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridines

E. F. Sagitovaa, D. N. Tomilina, O. V. Petrovaa, A. B. Budaeva, L. N. Sobeninaa, B. A. Trofimova, G. Q. Yangb, R. Hub

a A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
b Institute of Chemistry, Chinese Academy of Sciences, Beijing, China


Аннотация: Pharmaceutically relevant substituted 2-(pyrazol-5-yl)-4,5,6,7-tetrahydropyrrolo [3,2-c]pyridines have been assembled in good to excellent yields via the reaction of 2,2,6,6-tetramethylpiperidin-4-one oxime with acetylene, cross-coupling of the resulting 4,4,6,6-tetramethyl-4,5,6,7 tetrahydropyrrolo[3,2-c]pyridines with aroylbromoacetylenes, and reaction of the formed 2-(aroylethynyl)-4,4,6,6-tetramethyl-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridines with hydrazine.

Язык публикации: английский

DOI: 10.1016/j.mencom.2019.11.018



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