Metal-free synthesis of 3-trifluoromethyl-1,2,4-triazoles via multi-component reaction of trifluoroacetimidoyl chlorides, hydrazine hydrate and benzene-1,3,5-triyl triformate DOI Creative Commons

Binjie Wang,

Yue Sun,

Cheng An

и другие.

Frontiers in Chemistry, Год журнала: 2022, Номер 10

Опубликована: Сен. 20, 2022

A convenient approach for the construction of pharmaceutically valuable 3-trifluoromethyl-1,2,4-triazoles has been developed, which employs readily available trifluoroacetimidoyl chlorides, hydrazine hydrate and benzene-1,3,5-triyl triformate (TFBen) as starting materials. The multi-component reaction features broad substrate scope, high efficiency, scalability, providing a facile straightforward route to biologically important 3-trifluoromethyl-1,2,4-triazole scaffolds in moderate good yields. Considering its broad-spectrum pharmaceutical activity, method offers opportunity further study towards toxicity risk assessment structure-activity relationship pharmaceuticals containing trifluoromethyl-1,2,4-triazole cores.

Язык: Английский

Construction of trifluoromethyl-containing heterocycles from trifluoroacetimidoyl chlorides and derivatives DOI

Zuguang Yang,

Guangming Wei,

Zhengkai Chen

и другие.

Chemical Communications, Год журнала: 2023, Номер 59(33), С. 4872 - 4890

Опубликована: Янв. 1, 2023

Recent advances in the direct synthesis of trifluoromethyl-containing heterocycles from trifluoroacetimidoyl chlorides (TFAICs) and derivatives, including trifluoroacetimidohydrazides (TFAIHs) CF3-imidoyl sulfoxonium ylides (TFISYs), are systematically summarized discussed. The cascade annulation reactions synthons with suitable coupling partners have emerged as a powerful promising tool for construction variety trifluoromethyl-substituted heterocycles. Compared other building blocks, TFAICs derivatives notable merits easy availability handling, relative stability safety, high reactivity.

Язык: Английский

Процитировано

22

Metal-free synthesis of 3-trifluoromethyl-1,2,4-triazoles via multi-component reaction of trifluoroacetimidoyl chlorides, hydrazine hydrate and benzene-1,3,5-triyl triformate DOI Creative Commons

Binjie Wang,

Yue Sun,

Cheng An

и другие.

Frontiers in Chemistry, Год журнала: 2022, Номер 10

Опубликована: Сен. 20, 2022

A convenient approach for the construction of pharmaceutically valuable 3-trifluoromethyl-1,2,4-triazoles has been developed, which employs readily available trifluoroacetimidoyl chlorides, hydrazine hydrate and benzene-1,3,5-triyl triformate (TFBen) as starting materials. The multi-component reaction features broad substrate scope, high efficiency, scalability, providing a facile straightforward route to biologically important 3-trifluoromethyl-1,2,4-triazole scaffolds in moderate good yields. Considering its broad-spectrum pharmaceutical activity, method offers opportunity further study towards toxicity risk assessment structure-activity relationship pharmaceuticals containing trifluoromethyl-1,2,4-triazole cores.

Язык: Английский

Процитировано

2