Реакция #1145331

ord-e7a33e501a974c558bacdbe157c1e3da

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.WAITThe reaction mixture is stirrred for 4 hours
  2. 2
    Экстракцияextracted 2× with ethyl acetate
  3. 3
    ПромывкаThe combined organic layers are washed sequentially with brine, aqueous 2N hydrochloric acid
  4. 4
    Сушкаbrine, dried over sodium sulfate
  5. 5
    Фильтрацияfiltered
  6. 6
    Концентрированиеconcentrated in vacuo
  7. 7
    workup.ADDITIONTo the residue is added 15% aqueous potassium bicarbonate (5 mL) and methyl alcohol (3 mL)
  8. 8
    Температураheated
  9. 9
    Температураat reflux for 3 hours
  10. 10
    ТемператураAfter cooling
  11. 11
    Экстракцияthe reaction mixture is extracted with ethyl acetate
  12. 12
    Сушкаthe organic layer dried over sodium sulfate
  13. 13
    Фильтрацияfiltered
  14. 14
    Концентрированиеconcentrated 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 stirrred 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; (Compound 1) m.p. 130-132° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06515140B2uspto-grants-2003_02