Methane → Ethyl 1,2,3,6-tetrahydroazepino[4,5-B]indole-5-carboxylate

HRID 37912

반응식

HRID 37912 반응식
Cl.[NH2:2][CH2:3][CH2:4][C:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1.Br[CH2:15][C:16](=O)[C:17]([O:19][CH2:20][CH3:21])=[O:18].C>C(O)C>[CH2:4]1[C:5]2[C:13]3[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=3[NH:7][C:6]=2[C:16]([C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:15][NH:2][CH2:3]1

참가 물질

5

실험 절차

A mixture of tryptamine hydrochloride (1.96 g, 10 mmol), ethyl 3-bromopyruvate (1.67 mL, 1.2 equiv) and decolorizing charcoal (0.5 g) in absolute ethanol was heated to reflux under nitrogen overnight. TEA was added and the reaction mixture was heated to reflux for another 7.5 hours. After cooling, charcoal was removed by filtration and washed with ethanol. The filtrate was concentrated under vacuum and diluted with water (20 mL). It was then extracted by EtOAc (3×30 mL) and the combined organic layers were washed with brine and dried over MgSO4. Evaporation of solvent and recrystallization from DCM-Hexane gave the title compound (1.17 g). 1H-NMR (CDCl3): δ 10.49 (1 H, br s), 7.79 (1H, d), 7.43 (1H, d), 7.43 (1 H, d), 7.06 (2H, m), 5.27 (1H, br s), 4.29 (2H, q) 3.58 (2H, m), 3.17 (2H, m), 1.36 (3H, t); MS (ES): 257 (MH+).

후처리

  1. temperaturewas heated
  2. temperatureto reflux under nitrogen overnight
  3. additionTEA was added
  4. temperaturethe reaction mixture was heated
  5. temperatureto reflux for another 7.5 hours
  6. temperatureAfter cooling
  7. customcharcoal was removed by filtration
  8. washwashed with ethanol
  9. concentrationThe filtrate was concentrated under vacuum
  10. additiondiluted with water (20 mL)
  11. extractionIt was then extracted by EtOAc (3×30 mL)
  12. washthe combined organic layers were washed with brine
  13. dry with materialdried over MgSO4
  14. customEvaporation of solvent and recrystallization from DCM-Hexane

출처 및 근거

ORD 기록
ord-e9ef8ddee810448cb1d50790e723ab4a
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08524704B2

연결된 노트

불러오는 중…