Continuous Flow Synthesis of N-Sulfonyl-1,2,3-triazoles for Tandem Relay Cu/Rh Dual Catalysis

被引:0
作者
Kwon, Yong-Ju [1 ]
Lee, Sang-gi [1 ]
Kim, Won-Suk [1 ]
机构
[1] Ewha Womans Univ, Dept Chem & Nanosci, Seoul 03760, South Korea
基金
新加坡国家研究基金会;
关键词
AZIDE-ALKYNE CYCLOADDITIONS; TERMINAL ALKYNES; 1,3-DIPOLAR CYCLOADDITIONS; CHEMISTRY; TRANSANNULATION; 1,2,3-TRIAZOLES; FORMAMIDES; REACTORS; BONDS; CUAAC;
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The continuous flow synthesis of N-sulfonyl-1,2,3triazoles, which are convenient reactive azavinyl carbene precursors, for tandem relay Cu/Rh dual catalysis has been developed. Most reactions readily proceeded at 75 degrees C in a short residence time of 13.09 min in the presence of 2.5 mol % of CuTC. The scope of the reactions was explored by synthesizing diversely functionalized N-sulfonyl and sulfamoyl triazoles in yields ranging from 92 to 98%. To demonstrate the scalability of the process, the reaction was conducted on a 5.4 mmol scale with residence and collection times of 13.09 and 60 min, respectively. Furthermore, a series of controlled experiments were performed to investigate the compatibility of Cu and Rh in a batch or a continuous flow system. Finally, the first integrated flow system using the azavinyl carbene intermediate under the tandem relay Cu/Rh dual catalysis was developed alkynes and sulfonyl azides.
引用
收藏
页码:1200 / 1214
页数:15
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