Potassium Carbonate → tert-butyl 4-(1-ethylpropyl)-3-(2-isopropoxy-2-oxoethyl)-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxylate

HRID 1698570ノート

反応式

HRID 1698570 の反応式
[CH2:1]([CH:3]([C:6]1[C:14]2[NH:13][C:12](=[O:15])[N:11]([C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[C:10]=2[CH:9]=[CH:8][CH:7]=1)[CH2:4][CH3:5])[CH3:2].C(=O)([O-])[O-].[K+].[K+].Br[CH2:30][C:31]([O:33][CH:34]([CH3:36])[CH3:35])=[O:32]>CN(C)C=O.O>[CH2:1]([CH:3]([C:6]1[C:14]2[N:13]([CH2:30][C:31]([O:33][CH:34]([CH3:36])[CH3:35])=[O:32])[C:12](=[O:15])[N:11]([C:16]([O:18][C:19]([CH3:20])([CH3:22])[CH3:21])=[O:17])[C:10]=2[CH:9]=[CH:8][CH:7]=1)[CH2:4][CH3:5])[CH3:2]

参加物

6

実験手順

To a suspension of tert-butyl 4-(1-ethylpropyl)-2-oxo-2,3-dihydro-1H-benzimidazole-1-carboxylate (7.70 g, 25.3 mmol) in N,N-dimethylformamide (50 mL) was added potassium carbonate (3.84 g, 27.8 mmol) and isopropyl bromoacetate (3.60 ml, 27.8 mmol), and the mixture was stirred at room temperature for 5 hours. The reaction mixture was diluted with water and extracted with ethyl acetate (X2). The combined organic layer was washed with aqueous sodium chloride (X2) and brine (X1), dried over sodium sulfate and concentrated in vacuo. The residue was purified by silica gel column, chromatography eluting with a 5-20% ethyl acetate/hexane gradient mixture to give 8.95 g (22.1 mmol, 87.5%) of the title compound as a colorless oil.

後処理

  1. extractionextracted with ethyl acetate (X2)
  2. washThe combined organic layer was washed with aqueous sodium chloride (X2) 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 5-20% ethyl acetate/hexane gradient mixture

出典と根拠

ORDレコード
ord-2212780be9b04c6eab5b99d1fe4b765f
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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