Réaction #915

ord-952e75b6acac43568991fc07fe11133a

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05723410uspto-grants-1998_03