Unexpected hydrazine- and hydroxylamine-induced transformations of aza-14-crown-4 incorporating 4-oxopiperidine-3-carboxylate moiety

Reactions of aza-14-crown-4 incorporating 4-oxopiperidine-3-carboxylate moiety with hydrazine and hydroxylamine proceed at the functional groups. One unexpected product, cyclopenteno-13-crown-3 ether derivative, is formed when hydrazine hydrochloride is used, its formation occurring via deamination of the piperidine followed by the Nazarov reaction of the intermediate hydrazono diene. According to the QSAR through ADMET calculation, the synthesized compounds may show high potential for biological studies. © 2023

Авторы
Nguyen D.T. , Truong H.H. , Dao N.T. , Tran V.T.T. , Gorchakova O.S. , Le A.T.
Издательство
Royal Society of Chemistry
Номер выпуска
5
Язык
Английский
Страницы
708-710
Статус
Опубликовано
Том
33
Год
2023
Организации
  • 1 Faculty of Chemistry, VNU University of Science, Vietnam National University, Thanh Xuan, Hanoi, 100000, Viet Nam
  • 2 Peoples Friendship University of Russia (RUDN University), Moscow, 117198, Russian Federation
  • 3 ‘Sanofi-aventis group’ Representative office in Russia, Moscow, 125009, Russian Federation
Ключевые слова
azacrown ether; cyclopenteno-13-crown-3 ether; hydrazone; Nazarov reaction; piperidone
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