Pot, atom and step economic (PASE) assembly of salicylaldehydes, malononitrile dimer and 4-hydroxypyridine-2(1H)-ones into medicinally relevant 5H-chromeno[2,3-b]pyridine scaffold Научная публикация
Журнал |
Molecular Diversity
ISSN: 1573-501X , E-ISSN: 1381-1991 |
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Вых. Данные | Год: 2020, Том: 24, Номер: 3, Страницы: 617-626 Страниц : 10 DOI: 10.1007/s11030-019-09968-x | ||||
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Реферат:
The new multicomponent reaction (MCR) has been found: one-pot selective and efficient formation of the new 5-(4-hydroxy-2-oxo-1,2-dihydropyridin-3-yl)-substituted 5H-chromeno[2,3-b]pyridines in 61–97% yields directly from simple and easily available salicylaldehydes, malononitrile dimer and 4-hydroxypyridine-2(1H)-ones in small amount of pyridine–ethanol catalyst/solvent system. This complex “domino” transformation includes Knoevenagel condensation of salicylaldehyde with malononitrile dimer, Michael addition of 4-hydroxypyridine-2(1H)-one, double Pinner-type reaction cyclization and isomerization with following protonation. This facile multicomponent process opens a new way to 5-(4-hydroxy-2-oxo-1,2-dihydropyridin-3-yl)-substituted 5H-chromeno[2,3-b]pyridine systems, which are promising compounds for the treatment for human inflammatory TNFα-mediated diseases and different biomedical applications.
Библиографическая ссылка:
Elinson M.N.
, Vereshchagin A.N.
, Anisina Y.E.
, Krymov S.K.
, Fakhrutdinov A.N.
, Goloveshkin A.S.
, Egorov M.P.
Pot, atom and step economic (PASE) assembly of salicylaldehydes, malononitrile dimer and 4-hydroxypyridine-2(1H)-ones into medicinally relevant 5H-chromeno[2,3-b]pyridine scaffold
Molecular Diversity. 2020. V.24. N3. P.617-626. DOI: 10.1007/s11030-019-09968-x WOS Scopus OpenAlex
Pot, atom and step economic (PASE) assembly of salicylaldehydes, malononitrile dimer and 4-hydroxypyridine-2(1H)-ones into medicinally relevant 5H-chromeno[2,3-b]pyridine scaffold
Molecular Diversity. 2020. V.24. N3. P.617-626. DOI: 10.1007/s11030-019-09968-x WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: | WOS:000547921900003 |
Scopus: | 2-s2.0-85066975642 |
OpenAlex: | W2951415667 |