反応 #915

ord-952e75b6acac43568991fc07fe11133a

反応方程式

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
収率 21.4%
Cn1ccc(S(N)(=O)=O)c1Br
2-Bromo-1-methyl-1H-pyrrole-3-sulfonamide
収率 21.4%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

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

実験手順

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.

出典

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