反応式
[Br:1][C:2]1[CH:3]=[C:4]([N+:9]([O-])=O)[C:5]([Cl:8])=[N:6][CH:7]=1.[Cl-].[NH4+]>CO.ClCCl.[Zn]>[Br:1][C:2]1[CH:3]=[C:4]([NH2:9])[C:5]([Cl:8])=[N:6][CH:7]=1参加物
6
実験手順
To a solution of 5-bromo-2-chloro-3-nitropyridine (5.0 g, 21.1 mmol) in methanol (50 mL) and dichloromethane (5 mL) was added zinc (7.6 g, 115.8 mmol) and ammonium chloride (5.6 g, 105.3 mmol). The reaction mixture was stirred for 24 hours. The solids were removed by filtration and washed with dichloromethane. The filtrate was washed with water (50 mL), brine (50 mL), dried over sodium sulfate, filtered and concentrated to dryness under reduced pressure. The crude 5-bromo-2-chloropyridin-3-amine (4.2 g) was used without further purification. LCMS [M+H]: 207.
後処理
- customThe solids were removed by filtration
- washwashed with dichloromethane
- washThe filtrate was washed with water (50 mL), brine (50 mL)
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated to dryness under reduced pressure
- customThe crude 5-bromo-2-chloropyridin-3-amine (4.2 g) was used without further purification
出典と根拠
- ORDレコード
- ord-fb79ef3946d74492b5798e7221a26aa5
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08541407B2
関連ノート
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