Réaction #922

ord-4d0fbf7c4db24ef2820d2d87a9754e6c

Équation de réaction

CN(C)C(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
3-[[(1,1-dimethylethyl)amino]sulfonyl]-N,N,1-trimethyl-1H-pyrrole-2-carboxamide
O=C(O)C(F)(F)F
TFA
CN(C)C(=O)c1c(S(N)(=O)=O)ccn1C
title compound
Rendement 92.9%
CN(C)C(=O)c1c(S(N)(=O)=O)ccn1C
3 -(Aminosulfonyl)-N,N,1-trimethyl-1H-pyrrole-2-carboxamide
Rendement 92.9%

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 residue
  3. 3
    Autreremoved by evaporation
  4. 4
    Autreto remove residual TFA

Mode opératoire

To a solution of 5.63 g of 3-[[(1,1-dimethylethyl)amino]sulfonyl]-N,N,1-trimethyl-1H-pyrrole-2-carboxamide in 75 mL of methylene chloride was added 75 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 residue and removed by evaporation to remove residual TFA, affording 4.21 g of the title compound as a gray solid, m.p. 185°-190.5° C.

Source

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