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Dimethylformamide → tert-Butyl 2-(2-oxo-2,3-dihydrobenzo[d]imidazol-1-yl)ethylcarbamate

HRID 1984539
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반응식

HRID 1984539 반응식
[C:1]([O:5][C:6](=[O:18])[NH:7][CH2:8][CH2:9][NH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[NH2:17])([CH3:4])([CH3:3])[CH3:2].CN([CH:22]=[O:23])C>>[C:1]([O:5][C:6](=[O:18])[NH:7][CH2:8][CH2:9][N:10]1[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[NH:17][C:22]1=[O:23])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6228DimethylformamideHCID 28875325tert-Butyl 2-[(2-Aminophenyl)amino]ethylcarbamate

생성물 1

HCID 57428815tert-Butyl 2-(2-oxo-2,3-dihydrobenzo[d]imidazol-1-yl)ethylcarbamate수율 56%

실험 절차

A mixture of [2-(2-aminophenylamino)ethyl]carbamic acid t-butyl ester (3.85 g, 15.3 mmol) and 1,1-carbonyldiimidazole (CDI) (2.73 g, 16.8 mmol) in DMF are heated at 110°-120° C. until reaction is complete by TLC, cooled and extracted with EtOAc. The combined extracts are washed with water, dried over MgSO4 and concentrated in vacuo. The resultant residue is purified by flash chromatography (silica gel, 1:1 CH2Cl2: EtOAc as eluent) to give the title compound as a brown solid, 2.4 g (56% yield), identified by HPLC and mass spectral analyses.

후처리

  1. temperatureare heated at 110°-120° C. until reaction
  • temperaturecooled
  • extractionextracted with EtOAc
  • washThe combined extracts are washed with water
  • dry with materialdried over MgSO4
  • concentrationconcentrated in vacuo
  • customThe resultant residue is purified by flash chromatography (silica gel, 1:1 CH2Cl2: EtOAc as eluent)
  • 출처 및 근거

    ORD 기록
    ord-bf748a7269644748aa61c978748324c5
    출처 데이터셋
    uspto-grants-2009_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07544701B2

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