Реакция #592255

ord-e290cce8ef914ea8a3ff203da847e888

Уравнение реакции

CNC(=O)Cn1cc(C(=O)C(F)(F)F)c2ccc(Cl)cc21
2-[6-Chloro-3-(2,2,2-trifluoro-acetyl)-indol-1-yl]-N-methyl-acetamide
C[Si](C)(C)[O-].[Na+]
sodium trimethylsilanolate
CNC(=O)Cn1cc(C(=O)O)c2ccc(Cl)cc21
title compound
Выход 27.0%
CNC(=O)Cn1cc(C(=O)O)c2ccc(Cl)cc21
6-Chloro-1-methylcarbamoylmethyl-1H-indole-3-carboxylic acid
Выход 27.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Концентрированиеthe mixture was concentrated in vacuo
  2. 2
    Другоеpurified by prep

Методика

2-[6-Chloro-3-(2,2,2-trifluoro-acetyl)-indol-1-yl]-N-methyl-acetamide was suspensed in DCE and treated with (2.2 eq.) of sodium trimethylsilanolate. After shaking at room temperature for 20 min, the mixture was concentrated in vacuo and purified by prep. HPLC to give the title compound in 27% yield.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07781436B2uspto-grants-2010_08