2-Methoxy-3-nitropyridine → 3-Amino-2-methoxypyridine

HRID 70521

反応式

HRID 70521 の反応式
[CH3:1][O:2][C:3]1[C:8]([N+:9]([O-])=O)=[CH:7][CH:6]=[CH:5][N:4]=1.[H][H]>CO.[Pd]>[CH3:1][O:2][C:3]1[C:8]([NH2:9])=[CH:7][CH:6]=[CH:5][N:4]=1

参加物

5

反応物 2

HCID 2532192-Methoxy-3-nitropyridineHCID 178418361HCID 178418361、化合物

生成物 1

HCID 27374883-Amino-2-methoxypyridine収率 92%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

10% palladium-activated carbon (2.5 g) was added to a solution of commercially available 2-methoxy-3-nitropyridine (50.5 g) in methanol (500 mL), and the mixture was stirred for four hours in a hydrogen atmosphere. The reaction solution was filtered through celite, and then the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=8:1) to give 2-methoxypyridin-3-amine as a yellow powder (37.2 g, 92%).

後処理

  1. filtrationThe reaction solution was filtered through celite
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. customThe resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=8:1)

出典と根拠

ORDレコード
ord-1416a950087e4723ba3ed4261c7815ab
出典データセット
uspto-grants-2014_09
特許番号
US08822503B2

関連ノート

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