Реакция #911

ord-740719404b1e4815a4a77e34574adcd7

Уравнение реакции

COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
methyl 3-[[(1,1-dimethylethyl)amino]-sulfonyl]-1-methyl-1H-pyrrole-2-carboxylate
O=C(O)C(F)(F)F
trifluoroacetic acid
COC(=O)c1c(S(N)(=O)=O)ccn1C
title compound
COC(=O)c1c(S(N)(=O)=O)ccn1C
Methyl 3-(aminosulfonyl)-1-methyl-1H-pyrrole-2-carboxylate

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеThe gold solution was concentrated to an oily residue
  2. 2
    workup.ADDITIONDiethyl ether was added to the residue
  3. 3
    Другоеremoved by evaporation
  4. 4
    Другоеto remove residual TFA
  5. 5
    Фильтрацияfiltered

Методика

To a solution of 3.53 g of methyl 3-[[(1,1-dimethylethyl)amino]-sulfonyl]-1-methyl-1H-pyrrole-2-carboxylate in 40 mL, of methylene chloride under an nitrogen atmosphere was added 80 mL of trifluoroacetic acid (TFA). The gold solution was stirred at room temperature overnight ca. 16 hours. The gold solution was concentrated to an oily residue. Diethyl ether was added to the residue and removed by evaporation to remove residual TFA. The resulting solid was suspended in diethyl ether and filtered affording the title compound as a tan solid, m.p. 105°-107° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05723410uspto-grants-1998_03