Water → 4-Amino-1,3-dihydro-2H-benzimidazol-2-one

HRID 1528199노트

반응식

HRID 1528199 반응식
[C:1]1([NH2:9])[CH:6]=[CH:5][CH:4]=[C:3]([NH2:7])[C:2]=1[NH2:8].[OH2:10].[C:11](#N)C>>[NH2:7][C:3]1[C:2]2[NH:8][C:11](=[O:10])[NH:9][C:1]=2[CH:6]=[CH:5][CH:4]=1

참가 물질

4

실험 절차

0.53 g (6.5 mmol, 2 eq) of N—N′-carbonyliimidazole were added portionwise to 450.7 mg (3.24 mmol, 1 eq) of benzene-1,2,3-triamine in solution in 30 ml of acetonitrile. The reaction medium was stirred at ambient temperature for 6 hours and then heated at 70° C. overnight. The reaction was stopped by adding 50 ml of water and then extracted with ethyl acetate. The organic phases were combined, and dried over sodium sulfate. The solvents were evaporated off and then the residue was purified by chromatography on silica gel (dichloromethane/methanol/aqueous ammonia: 95/5/2). 229.9 mg of 4-amino-1,3-dihydrobenzoimidazol-2-one were obtained. Yield=42%.

후처리

  1. temperatureheated at 70° C. overnight
  2. extractionextracted with ethyl acetate
  3. dry with materialdried over sodium sulfate
  4. customThe solvents were evaporated off
  5. customthe residue was purified by chromatography on silica gel (dichloromethane/methanol/aqueous ammonia: 95/5/2)

출처 및 근거

ORD 기록
ord-161af9861d8f4d54b2657c2b6e23be57
출처 데이터셋
uspto-grants-2015_07
특허 번호
US09090596B2

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