Реакция #1062497
ord-855059b932ff43c288c4d093a3588177
Уравнение реакции
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1КонцентрированиеAfter concentrating in vacuo
- 2Промывкаwashed with 1.3M hydrochloric acid
- 3Сушкаwith aqueous sodium bicarbonate, dried over magnesium sulfate
- 4Фильтрацияfiltered
- 5Концентрированиеconcentrated in vacuo
- 6ДругоеRecrystallization from ethyl acetate
Методика
A mixture of 4-Oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid (179 mg, 1 mmol), p-anisidine (616 mg. 5 mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride [EDCI] (959 mg, 5 mmol) in 50% aqueous 1,4-dioxane (10 mL) was stirred at ambient temperature for 17 h. After concentrating in vacuo, the residue was taken up in 10% methanol in ethyl acetate, washed with 1.3M hydrochloric acid then with aqueous sodium bicarbonate, dried over magnesium sulfate, filtered, and concentrated in vacuo. Recrystallization from ethyl acetate afforded N-(4-Methoxyphenyl)-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamide (Compound 1); mp 219°-220° C.