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Two-Stage Synthesis of 3-(4-Hydroxyphenyl)-1′,3′,6-trimethyl-2′H,3H,4H-spiro[furo[3,2-c]pyran-2,5′-pyrimidine]-2′,4,4′,6′(1′H,3′H)-tetraone Научная публикация

Журнал Molbank
ISSN: 1422-8599
Вых. Данные Год: 2026, Том: 2026, Номер: 2, Номер статьи : M2148, Страниц : DOI: 10.3390/m2148
Ключевые слова 4-hydroxybenzaldehyde; N,N′-dimethylbarbituric acid; 4-hydroxy-6-methyl- 2H-pyran-2-one; morpholine; N-bromosuccinimide; ionic scaffold; spiro[furo[3,2-c]pyran; tandem Knoevenagel–Michael reaction; cyclization
Авторы Elinson Michail N. 1 , Kalashnikova Varvara M. 1 , Ryzhkova Yuliya E. 1 , Rakitin Oleg A. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry Russian Academy of Sciences, 47 Leninsky Prospekt, 119991 Moscow, Russia

Реферат: Spirocyclic compounds are experiencing a research surge due to their unique 3D structure, offering enhanced pharmacological, industrial, and material applications. They are increasingly used in medicinal chemistry to improve drug-like properties, such as solubility and target binding, and are also being utilized for advanced material applications, including electronics and photonics. In this communication, 3-(4-hydroxyphenyl)-1′,3′,6-trimethyl- 2′H,3H,4H-spiro[furo[3,2-c]pyran-2,5′-pyrimidine]-2′,4,4′,6′(1′H,3′H)-tetraone was prepared via a two-stage transformation including a tandem Knoevenagel–Michael reaction and NBSinduced cyclization. At the first stage, a previously unknown ionic scaffold, morpholin-4- ium 5-((4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)(4-hydroxyphenyl)methyl)-1,3-dimethyl- 2,6-dioxo-1,2,3,6-tetrahydropyrimidin-4-olate was also isolated. Structures of the newly synthesized compounds were established by 1H and 13C NMR, IR spectroscopy, highresolution mass spectrometry, and elemental analysis.
Библиографическая ссылка: Elinson M.N. , Kalashnikova V.M. , Ryzhkova Y.E. , Rakitin O.A.
Two-Stage Synthesis of 3-(4-Hydroxyphenyl)-1′,3′,6-trimethyl-2′H,3H,4H-spiro[furo[3,2-c]pyran-2,5′-pyrimidine]-2′,4,4′,6′(1′H,3′H)-tetraone
Molbank. 2026. V.2026. N2. M2148 . DOI: 10.3390/m2148 OpenAlex
Даты:
Поступила в редакцию: 28 янв. 2026 г.
Принята к публикации: 6 мар. 2026 г.
Опубликована online: 11 мар. 2026 г.
Идентификаторы БД:
≡ OpenAlex: W7134904376
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