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

Authors
Nguyen D.T. , Truong H.H. , Dao N.T. , Tran V.T.T. , Gorchakova O.S. , Le A.T.
Publisher
Royal Society of Chemistry
Issue number
5
Language
English
Pages
708-710
State
Published
Volume
33
Year
2023
Organizations
  • 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
Keywords
azacrown ether; cyclopenteno-13-crown-3 ether; hydrazone; Nazarov reaction; piperidone
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