Ammonium Chloride → 3-Amino-5-bromo-2-chloropyridine

HRID 44242

反応式

HRID 44242 の反応式
[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

  1. customThe solids were removed by filtration
  2. washwashed with dichloromethane
  3. washThe filtrate was washed with water (50 mL), brine (50 mL)
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated to dryness under reduced pressure
  7. 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

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