Transition-Metal-Free (Hetero)arylsulfonylation of 1-Iodopyrrolo[1,2-a]quinoxalines

被引:0
|
作者
Ca, Thuy T. [1 ,2 ,3 ]
Le, Khanh T. M. [2 ,4 ]
Nguyen, Tung T. [1 ,2 ,4 ]
Chau, Ngoc D. Q. [1 ,2 ]
机构
[1] Ho Chi Minh City Univ Technol HCMUT, Fac Chem Engn, 268 Ly Thuong Kiet,Dist 10, Ho Chi Minh City, Vietnam
[2] Vietnam Natl Univ Ho Chi Minh City, Ho Chi Minh City, Vietnam
[3] Univ Med & Pharm, Fac Basic Sci, Ho Chi Minh City, Vietnam
[4] VNU HCM Key Lab Funct Organ Mat, Ho Chi Minh City, Vietnam
来源
CHEMISTRYSELECT | 2024年 / 9卷 / 26期
关键词
pyrrolo[1,2-a]quinoxaline; sulfonylation; arylsulfinate; metal-free; heteroarene; DERIVATIVES;
D O I
10.1002/slct.202401948
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We describe herein a method for transition-metal-free (hetero)arylsulfonylation of 1-iodopyrrolo[1,2-a]quinoxalines with sodium arylsulfinates. The corresponding aryl iodides were in situ prepared from eletrophilic iodination of C1-H bonds in pyrrolo[1,2-a]quinoxalines with N-iodosuccinimide. The ensuing sulfonylation only required DMSO as solvent and completed after 15 min. Many arylsulfinates bearing chloro, bromo, methylsufonyl, acetamide, and nitro groups were competent substrates. Heteroarylsulfonylation of pyrrolo[1,2-a]quinoxalines were also feasible.
引用
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页数:5
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