Cesium carbonate → Tert-butyl 3-tert-butoxycarbonylmethyl-5-chloro-2-oxo-2,3-dihydrobenzimidazole-1-carboxylate

HRID 1631948노트

반응식

HRID 1631948 반응식
[Cl:1][C:2]1[CH:18]=[CH:17][C:5]2[N:6]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[C:7](=[O:9])[NH:8][C:4]=2[CH:3]=1.Br[CH2:20][C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22].C(=O)([O-])[O-].[Cs+].[Cs+]>C(#N)C>[C:24]([O:23][C:21]([CH2:20][N:8]1[C:4]2[CH:3]=[C:2]([Cl:1])[CH:18]=[CH:17][C:5]=2[N:6]([C:10]([O:12][C:13]([CH3:14])([CH3:15])[CH3:16])=[O:11])[C:7]1=[O:9])=[O:22])([CH3:27])([CH3:26])[CH3:25]

참가 물질

5

실험 절차

A mixture of 4.00 g (14.9 mmol) of tert-butyl 5-chloro-2-oxo-2,3-dihydrobenzimidazole-1-carboxylate (VIa), 3.19 g (16.4 mmol) of tert-butyl bromoacetate and 7.28 g (22.3 mmol) of cesium carbonate in acetonitrile (80 ml) was heated under reflux for 3 h. The solvent was removed in vacuo, the residue was mixed with water, and the aqueous mixture was extracted four times with ethyl acetate. The combined organic phases were washed with saturated NaCl solution and dried over magnesium sulfate, and the solvent was removed in vacuo. The residue was purified by chromatography on silica gel (mobile phase gradient 0-5% ethyl acetate in dichloromethane).

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 3 h
  3. customThe solvent was removed in vacuo
  4. additionthe residue was mixed with water
  5. extractionthe aqueous mixture was extracted four times with ethyl acetate
  6. washThe combined organic phases were washed with saturated NaCl solution
  7. dry with materialdried over magnesium sulfate
  8. customthe solvent was removed in vacuo
  9. customThe residue was purified by chromatography on silica gel (mobile phase gradient 0-5% ethyl acetate in dichloromethane)

출처 및 근거

ORD 기록
ord-780528ff1e4f454b977113e63bbb71a1
출처 데이터셋
uspto-grants-2014_07
특허 번호
US08791148B2

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