Methyl iodide → 6-Bromo-3-methoxy-1-phenyl-1H-indazole
反応式
[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6](=[O:17])[NH:7][N:8]2[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:4][CH:3]=1.[C:18](=O)([O-])[O-].[K+].[K+].CI>CN(C)C=O>[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([O:17][CH3:18])=[N:7][N:8]2[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:4][CH:3]=1参加物
反応条件
- 温度
- 80 °C
実験手順
Into a 100-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 6-bromo-1-phenyl-1,2-dihydroindazol-3-one (5 g, 17.30 mmol, 1.00 equiv) in N,N-dimethylformamide (50 mL), potassium carbonate (3.7 g, 34.91 mmol, 2.00 equiv), CH3I (2.7 g, 19.01 mmol, 1.10 equiv). The resulting solution was stirred for 3 h at 80° C. in an oil bath. The reaction was then quenched by the addition of water (100 mL). The resulting solution was extracted with ethyl acetate (3×150 mL) and the organic layers combined, dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:40) to yield 6-bromo-3-methoxy-1-phenyl-1H-indazole as a yellow solid.
後処理
- customInto a 100-mL 3-necked round-bottom flask purged
- temperaturemaintained with an inert atmosphere of nitrogen
- customThe reaction was then quenched by the addition of water (100 mL)
- extractionThe resulting solution was extracted with ethyl acetate (3×150 mL)
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated under vacuum
出典と根拠
- ORDレコード
- ord-ff37fbe0da8c47dbbbc08727f09a4bd9
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08822447B2
反応ノート
読み込み中…