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Sodium hydride → HCID 22327360、化合物

HRID 495650
ノート
印刷プレビュー

反応式

HRID 495650 の反応式
[NH2:1][C:2]1[CH:7]=[C:6]([NH2:8])[CH:5]=[C:4]([C:9]([F:12])([F:11])[F:10])[C:3]=1[N:13]([C:19]1[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][C:20]=1[Cl:26])[C:14](=[O:18])OCC.[H-].[Na+].C(=O)(O)[O-].[Na+]>C(O)C>[NH2:8][C:6]1[CH:5]=[C:4]([C:9]([F:10])([F:11])[F:12])[C:3]2[N:13]([C:19]3[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][C:20]=3[Cl:26])[C:14](=[O:18])[NH:1][C:2]=2[CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 24758Sodium hydrideHCID 516892Sodium BicarbonateHCID 22327372HCID 22327372、化合物

生成物 1

HCID 22327360HCID 22327360、化合物収率 79.3%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Ethyl 2,4-diamino-6-(trifluoromethyl)phenyl(2,4-dichlorophenyl)carbamate (1.1454 g) was dissolved in ethanol (20 ml), and to the solution was added sodium hydride (112.2 mg). The reaction mixture was heated at reflux for 6 hours. After allowing to cool, to the reaction mixture was added saturated aqueous sodium bicarbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. The resultant residue was purified by silica gel column (60 g, CHCl3:methanol=10:1→5:1) to give the title compound (0.8058 g, 79%).

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 6 hours
  3. temperatureto cool, to the reaction mixture
  4. extractionthe mixture was extracted with ethyl acetate
  5. washThe organic layer was washed with saturated brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe resultant residue was purified by silica gel column (60 g, CHCl3:methanol=10:1→5:1)

出典と根拠

ORDレコード
ord-e1257daee7ab48e89a4ecf30d7e85b4c
出典データセット
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06939887B2

反応ノート

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