Synthesis and Properties of 3-Substituted 2H-Chromen-2-ones

Abstract: The condensation of salicylaldehyde with CH acids [p-methoxyacetoacetanilide, ethyl3-amino-3-sulfanylidenepropanoate, 3-amino-N-aryl-3-sulfanylidenepropanamides, and ethyl 2-(1,3-thiazol-2- and-4-yl)acetates] afforded 3-substituted chromen-2-ones. Some properties of theproducts were studied. The structures of3-[4-(4-chlorophenyl)-1,3-thiazol-2-yl]-2H-chromen-2-one, 2-oxo-2H-chromene-3-carboxamide, and 2-imino-N-(2-methoxyphenyl)-2H-chromene-3-carboxamide were determined by X-ray analysis. © 2020, Pleiades Publishing, Ltd.

Авторы
Dyachenko I.V.1 , Dyachenko V.D.1 , Dorovatovsky P.V.2 , Khrustalev V.N. 3, 4 , Nenaidenko V.G. 5
Журнал
Russian Journal of Organic Chemistry
Номер выпуска
7
Язык
Английский
Страницы
1123-1131
Статус
Опубликовано
Ссылка
Внешняя ссылка
DOI
10.1134/S1070428020070015
Том
56
Год
2020
Организации
  • 1 Taras Shevchenko Lugansk National University, Lugansk, 91011, Ukraine
  • 2 “Kurchatov Institute” National Research Center, Moscow, 123182, Russian Federation
  • 3 People’s Friendship University of Russia, Moscow, 117198, Russian Federation
  • 4 Zelinsky Institute of Organic Chemistry, Russian Academy ofSciences, Moscow, 119991, Russian Federation
  • 5 Faculty of Chemistry, Moscow State University, Moscow, 119991, Russian Federation
Ключевые слова
2H-chromen-2-one (coumarin); 3-amino-N-aryl-3-sulfanylidenepropanamide; ethyl 2-(1,3-thiazol-2-yl)acetate; ethyl 3-amino-3-sulfanylidenepropanoate; p-methoxyacetoacetanilide; X-ray analysis
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