Chlorosuccinimide → Isopropyl [4-chloro-7-(1-ethylpropyl)-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl]acetate

HRID 1698572ノート

反応式

HRID 1698572 の反応式
[CH:1]([O:4][C:5](=[O:22])[CH2:6][N:7]1[C:11]2[C:12]([CH:16]([CH2:19][CH3:20])[CH2:17][CH3:18])=[CH:13][CH:14]=[CH:15][C:10]=2[NH:9][C:8]1=[O:21])([CH3:3])[CH3:2].[Cl:23]N1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl.C(=O)([O-])O.[Na+].N(C(C)(C)C#N)=NC(C)(C)C#N>[CH:1]([O:4][C:5](=[O:22])[CH2:6][N:7]1[C:11]2[C:12]([CH:16]([CH2:19][CH3:20])[CH2:17][CH3:18])=[CH:13][CH:14]=[C:15]([Cl:23])[C:10]=2[NH:9][C:8]1=[O:21])([CH3:2])[CH3:3]

参加物

6

反応条件

温度
70 °C

実験手順

To a solution of isopropyl[7-(1-ethylpropyl)-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl]acetate (5.29 g, 17.4 mmol) in carbon tetrachloride (350 mL) was added N-chlorosuccinimide (2.55 g, 19.1 mmol) and 2,2′-azobisisobutyronitrile (86 mg, 0.522 mmol), and the mixture was stirred at 70° C. for 3 days. The reaction mixture was diluted with saturated aqueous sodium hydrogen carbonate and extracted with dichloromethane (X2). The combined organic layer was washed with water (X1) and brine (X1), dried over sodium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with a 10-50% ethyl acetate/hexane gradient mixture to give 3.83 g (11.3 mmol, 65.0%) of the title compound as a colorless solid.

後処理

  1. extractionextracted with dichloromethane (X2)
  2. washThe combined organic layer was washed with water (X1) and brine (X1)
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by silica gel column chromatography
  6. washeluting with a 10-50% ethyl acetate/hexane gradient mixture

出典と根拠

ORDレコード
ord-5c11c799a533448cbc62c47839faa704
出典データセット
uspto-grants-2012_04
特許番号
US08163935B2

反応ノート

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