Water → N-(2-chloro-5-fluoropyridin-3-yl)-2-methylacrylamide
反応式
[Cl:1][C:2]1[C:7]([NH2:8])=[CH:6][C:5]([F:9])=[CH:4][N:3]=1.O.[C:11](OCC)(=[O:13])C.N1[CH:22]=[CH:21][CH:20]=CC=1>CC(=C)C(Cl)=O>[Cl:1][C:2]1[C:7]([NH:8][C:11](=[O:13])[C:21]([CH3:20])=[CH2:22])=[CH:6][C:5]([F:9])=[CH:4][N:3]=1参加物
実験手順
To a solution of 1.2 g of 2-chloro-5-fluoropyridin-3-amine in 5 mL of pyridine, 0.86 mL of 2-methylacryloyl chloride was added under cooling with ice, and the mixture was stirred at room temperature for 30 minutes. To the reaction mixture, water and ethyl acetate were added, the organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed sequentially with water and a saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The resultant residue was purified by flash silica gel column chromatography using gradient elution with hexane:ethyl acetate=100:0 to 50:50 to obtain 1.1 g of N-(2-chloro-5-fluoropyridin-3-yl)-2-methylacrylamide as a colorless oily substance.
後処理
- temperatureunder cooling with ice
- customthe organic layer was separated
- extractionthe aqueous layer was extracted with ethyl acetate
- washthe resultant solution was washed sequentially with water
- dry with materiala saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate
- distillationthe solvent was distilled off under reduced pressure
- customThe resultant residue was purified by flash silica gel column chromatography
- washelution with hexane
出典と根拠
- ORDレコード
- ord-5c7a979a59924878985898ffc68cc546
- 出典データセット
- uspto-grants-2012_07
- 特許番号
- US08211908B2
反応ノート
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