2-Methoxy-3-methyl-5-nitropyridine → 6-Methoxy-5-methylpyridin-3-amine

HRID 505379ノート

反応式

HRID 505379 の反応式
[CH3:1][O:2][C:3]1[C:8]([CH3:9])=[CH:7][C:6]([N+:10]([O-])=O)=[CH:5][N:4]=1>CO>[CH3:1][O:2][C:3]1[N:4]=[CH:5][C:6]([NH2:10])=[CH:7][C:8]=1[CH3:9]

参加物

3

反応物 1

HCID 407869042-Methoxy-3-methyl-5-nitropyridine

生成物 1

HCID 407869036-Methoxy-5-methylpyridin-3-amine収率 93%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

2-Methoxy-3-methyl-5-nitropyridine (1.63 g, 9.71 mmol) was dissolved in methanol (50 ml), 10% Pd-on-carbon powder (50% water content article) (800 mg) was added, and stirred under hydrogen atmosphere for 2 hours and 10 minutes. After the reaction was completed, celite filtration was carried out, the solvent was evaporated, thereby yielding the title compound (1.25 g, 0.90 mmol, 93%) as a blue oily substance.

後処理

  1. filtrationcelite filtration
  2. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-f2060dff5f9e46628d01dd91f5a52398
出典データセット
uspto-grants-2010_08
特許番号
US07781452B2

反応ノート

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