Реакция #1350574
ord-afaf075ecc404ad580a3fdea35c06371
Уравнение реакции
3-(3-aminophenyl)-4-bromo-1-methylpyrazole
triethylamine
4-trifluoromethoxyphenylacetic acid
HBTU
HOBT
→
title compound
Выход 68.0%
N-[3-(4-bromo-1-methylpyrazol-3-yl)phenyl]-2-[4-(trifluoromethoxy)phenyl]acetamide
Выход 68.0%
Реактанты
Реагенты
Нет
Условия реакции
Температура
70°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Другоеquenched with aqueous sodium bicarbonate solution
- 2workup.ADDITIONEthyl acetate was added
- 3Другоеthe organic phase separated
- 4Промывкаwashed with water (×3), brine
- 5Сушкаdried (MgSO4)
- 6Другоеevaporated
Методика
A solution of 3-(3-aminophenyl)-4-bromo-1-methylpyrazole (35 mg, 0.14 mmol) and triethylamine (23 μL, 0.17 mmol) in DMF (0.5 mL) was added in one portion to a stirred solution of 4-trifluoromethoxyphenylacetic acid (31 mg, 0.14 mmol), HBTU (53 mg, 0.14 mmol) and HOBT (19 mg, 0.14 mmol) in DMF (1 mL). The mixture was heated at 70° C. for 24 h and then quenched with aqueous sodium bicarbonate solution. Ethyl acetate was added and the organic phase separated, washed with water (×3), brine, dried (MgSO4) and evaporated. Chromatography on flash silica (50% EtOAc/hexane) gave the title compound as a colourless solid (43 mg, 68%), m.p. 141.2-142.5° C. (EtOAc/hexane).