Реакция #670020

ord-0a149b95846741138cba0fb4272fea21

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеAfter concentrating in vacuo
  2. 2
    Промывкаwashed with 1.3M hydrochloric acid
  3. 3
    Сушкаwith aqueous sodium bicarbonate, dried over magnesium sulfate
  4. 4
    Фильтрацияfiltered
  5. 5
    Концентрированиеconcentrated in vacuo
  6. 6
    ДругоеRecrystallization 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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05925770uspto-grants-1999_07