Dimethylformamide → 3-(Aminomethyl)-6-methyl-4-propylpyridin-2(1H)-oneacetate

HRID 593886

반응식

HRID 593886 반응식
[H-].[Na+].[Br:3][C:4]1[CH:5]=[C:6]([C:13]([O:15][CH3:16])=[O:14])[C:7]2[CH:8]=[CH:9][NH:10][C:11]=2[CH:12]=1.Br[CH:18]([CH2:20][CH3:21])[CH3:19].[CH3:22][N:23]([CH:25]=[O:26])C>O>[Br:3][C:4]1[CH:5]=[C:6]([C:13]([O:15][CH3:16])=[O:14])[C:7]2[CH:8]=[CH:9][N:10]([CH:18]([CH2:20][CH3:21])[CH3:19])[C:11]=2[CH:12]=1.[NH2:10][CH2:9][C:8]1[C:25](=[O:26])[NH:23][C:22]([CH3:18])=[CH:11][C:7]=1[CH2:6][CH2:5][CH3:4]

참가 물질

7

실험 절차

To a stirred suspension of sodium hydride (5.66 g, 141.7 mmol) in DMF (100 mL) was added a solution of methyl 6-bromo-1H-indole-4-carboxylate (4) (30 g, 118.1 mmol) in DMF (50 mL) at 0° C. and stirred for 20 min. Then 2-Bromo butane (29.1 g, 212.5 mmol) was added at 0° C. and the reaction mixture was stirred at room temperature for 16 h. The reaction mixture was diluted with cold water and extracted with ethyl acetate (4×150 mL). The combined organic layer was washed with cold water (150 mL), brine (100 mL) and dried over anhydrous Na2SO4 and concentrated under reduced pressure to afford crude, which was purified by column chromatography over silica gel (60-120 mesh) using 5% EtOAc: Pet ether as eluent to afford the title compound methyl 6-bromo-1-sec-butyl-1H-indole-4-carboxylate, 5 (14 g, 40.1%) as pale yellow solid. 1H NMR (CDCl3, 400 MHz) δ 0.843-0.870 (m, 3H), 1.512 (d, J=6.4 Hz, 3H), 1.844-1.926 (m, 2H), 3.976 (s, 3H), 4.333-4.385 (m, 1H), 7.132 (d, J=3.2 Hz, 1H), 7.302 (d, J=3.6 Hz, 1H), 7.707 (s, 1H), 7.984 (d, J=1.6 Hz, 1H).

후처리

  1. stirringthe reaction mixture was stirred at room temperature for 16 h
  2. extractionextracted with ethyl acetate (4×150 mL)
  3. washThe combined organic layer was washed with cold water (150 mL), brine (100 mL)
  4. dry with materialdried over anhydrous Na2SO4
  5. concentrationconcentrated under reduced pressure
  6. customto afford crude, which
  7. customwas purified by column chromatography over silica gel (60-120 mesh)

출처 및 근거

ORD 기록
ord-95d8b57fcee84a5a8c10e0d2fd43dc31
출처 데이터셋
uspto-grants-2016_01
특허 번호
US09242962B2

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