HCID 18953543、化合物 → 4-(1H-imidazol-1-yl)pyridin-3-amine

HRID 1491636ノート

反応式

HRID 1491636 の反応式
[N:1]1([C:6]2[CH:11]=[CH:10][N:9]=[CH:8][C:7]=2[N+:12]([O-])=O)[CH:5]=[CH:4][N:3]=[CH:2]1.[H][H]>C(O)C.[C].[Pd]>[NH2:12][C:7]1[CH:8]=[N:9][CH:10]=[CH:11][C:6]=1[N:1]1[CH:5]=[CH:4][N:3]=[CH:2]1

参加物

5

反応物 2

HCID 18953543HCID 18953543、化合物HCID 178418361HCID 178418361、化合物2 回

生成物 1

HCID 189535484-(1H-imidazol-1-yl)pyridin-3-amine収率 91.9%

試薬・触媒・溶媒 2

HCID 178418390HCID 178418390、化合物触媒HCID 702Ethanol溶媒

実験手順

4-(1-Imidazolyl)-3-nitropyridine (2.10 g, 11.0 mmol) was dissolved in 20 ml of ethanol. After the atmosphere was replaced with nitrogen, 0.25 g of 10% palladium-carbon was added thereto. After the atmosphere was replaced with hydrogen, hydrogen addition was conducted with stirring at room temperature for 3 days. Palladium-carbon was removed by filtration and the filtered cake was washed with ethanol. The filtrate and the washings were combined and then concentrated. The residue was purified by silica gel column chromatography [eluent: dichloromethane:methanol=8:1-6:1 (v/v)] to obtain 1.62 g of a light brown solid (yield: 91.6%).

後処理

  1. additionwas added
  2. customPalladium-carbon was removed by filtration
  3. washthe filtered cake was washed with ethanol
  4. concentrationconcentrated
  5. customThe residue was purified by silica gel column chromatography [eluent: dichloromethane:methanol=8:1-6:1 (v/v)]

出典と根拠

ORDレコード
ord-c9dfc296919e4e01a85f1da252008546
出典データセット
uspto-grants-1994_12
特許番号
US05371086

反応ノート

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