Реакция #1267677
ord-d0f47cb2c9114d63904c6a3af04d5fcd
Уравнение реакции
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Концентрированиеconcentrated in vacuo
- 2ТемператураThe residue was cooled in an ice water bath
- 3workup.ADDITIONaqueous 3.6 N hydrochloric acid was added
- 4Другоеthe precipitate collected
- 5Промывкаrinsed with aqueous 3.6 N hydrochloric acid
- 6Сушкаwater and dried
- 7ДругоеRecrystallization from ethyl alcohol
Методика
A mixture of 4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxylic acid (179 mg, 1 mmol), aniline (0.46 mL, 5^ mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (959 mg, 5 mmol) in 50% aqueous dioxane (10 mL) was allowed to stir at ambient temperature for 17.5 hours, then concentrated in vacuo. The residue was cooled in an ice water bath, aqueous 3.6 N hydrochloric acid was added, and the precipitate collected, rinsed with aqueous 3.6 N hydrochloric acid then water and dried. Recrystallization from ethyl alcohol afforded N-phenyl-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamide (Compound 35) (164 mg). mp 225-226° C.