2-Fluoropyridine → 2-Methyl-1-(pyridin-2-yl)-1H-benzimidazole

HRID 382543

반응식

HRID 382543 반응식
[CH3:1][C:2]1[NH:6][C:5]2[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=2[N:3]=1.[H-].[Na+].F[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=1>CC(N(C)C)=O>[CH3:1][C:2]1[N:6]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=2)[C:5]2[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=2[N:3]=1

참가 물질

5

반응 조건

온도
100 °C

실험 절차

To a stirred solution of 2-methyl-1H-benzimidazole (6.61 g, 50 mmol) in dimethylacetamide (40 ml) at room temperature under a nitrogen atmosphere was added sodium hydride (2.40 g, 60 mmol) in portions during 15 min. At the point where the reaction mixture was too viscous to stir, the reaction was diluted with 100 ml of dimethylacetamide. After 50 min., a solution of 2-fluoropyridine (5.83 g, 60 mmol) in dimethylacetamide (30 ml) was added during 15 min. The resulting mixture was heated at 100° C. for 2 h and then to reflux for about 4 h. Volatiles were removed by evaporation under reduced pressure. The residue was dissolved into ethyl acetate (200 ml) and washed consecutively with water (3×100 ml) and brine (100 ml). The organic layer was dried (magnesium sulfate) and concentrated to dryness. Purification by column chromatography (silica gel, 300 g; n-hexane/ethyl acetate (17/3)) yielded 7.46 g (71%) of the titled compound as a light yellow liquid.

후처리

  1. temperatureto reflux for about 4 h
  2. customVolatiles were removed by evaporation under reduced pressure
  3. dissolutionThe residue was dissolved into ethyl acetate (200 ml)
  4. washwashed consecutively with water (3×100 ml) and brine (100 ml)
  5. dry with materialThe organic layer was dried (magnesium sulfate)
  6. concentrationconcentrated to dryness
  7. customPurification by column chromatography (silica gel, 300 g; n-hexane/ethyl acetate (17/3))

출처 및 근거

ORD 기록
ord-da2796e28f7b49cca2b2bf64a87bb8a6
출처 데이터셋
uspto-grants-2001_10
특허 번호
US06310079B1

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