反应 #915

ord-952e75b6acac43568991fc07fe11133a

反应方程式

Cn1ccc(S(=O)(=O)NC(C)(C)C)c1Br
2-bromo-N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide
O=C(O)C(F)(F)F
TFA
Cn1ccc(S(N)(=O)=O)c1Br
title compound
收率 21.4%
Cn1ccc(S(N)(=O)=O)c1Br
2-Bromo-1-methyl-1H-pyrrole-3-sulfonamide
收率 21.4%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩The reaction mixture was concentrated in vacuo
  2. 2
    workup.ADDITIONThree portions of diethyl ether were added to the crude residue
  3. 3
    其他was removed by evaporation
  4. 4
    其他to remove residual TFA, which

实验过程

To a solution of 7.11 g (24 mmol) of 2-bromo-N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 50 mL methylene chloride under a nitrogen atmosphere was added 50 mL of TFA. The reaction mixture was allowed to stir at room temperature overnight ca. 16 hours. The reaction mixture was concentrated in vacuo. Three portions of diethyl ether were added to the crude residue and was removed by evaporation to remove residual TFA, which yielded 1.23 g of the title compound as a light brown solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05723410uspto-grants-1998_03