Реакция #439085
ord-13e4e3d37f34436e84f83d2e550e761c
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1workup.STIRRINGThe reaction mixture is stirred for 4 hours
- 2Экстракцияextracted 2× with ethyl acetate
- 3ПромывкаThe combined organic layers are washed sequentially with brine, aqueous 2N hydrochloric acid
- 4Сушкаbrine, dried over sodium sulfate
- 5Фильтрацияfiltered
- 6Концентрированиеconcentrated in vacuo
- 7workup.ADDITIONTo the residue is added 15% aqueous potassium bicarbonate (5 mL) and methyl alcohol (3 mL)
- 8Температураheated
- 9Температураat reflux for 3 hours
- 10ТемператураAfter cooling
- 11Экстракцияthe reaction mixture is extracted with ethyl acetate
- 12Сушкаthe organic layer dried over sodium sulfate
- 13Фильтрацияfiltered
- 14Концентрированиеconcentrated in vacuo
Методика
To a stirred solution of 4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid (100 mg, 0.6 mmol) and triethylamine (0.15 mL, 1.1 mmol) in N,N-dimethylformamide (5 mL) at 0° C. is added ethyl chloroformate (0.1 mL, 1.1 mmol). After stirring an additional 1 hour, 3-(N-trifluoroacetyl-(methylaminomethyl)aniline (0.3 g, 1.3 mmol) is added. The reaction mixture is stirred for 4 hours, then poured into saturated aqueous ammonium chloride and extracted 2× with ethyl acetate. The combined organic layers are washed sequentially with brine, aqueous 2N hydrochloric acid, then brine, dried over sodium sulfate, filtered, and concentrated in vacuo. To the residue is added 15% aqueous potassium bicarbonate (5 mL) and methyl alcohol (3 mL), then heated at reflux for 3 hours. After cooling, the reaction mixture is extracted with ethyl acetate, the organic layer dried over sodium sulfate, filtered, and concentrated in vacuo to give N[3-(methylaminomethyl)phenyl]-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamide. m.p. 130-132° C.