Aminoacetaldehyde dimethyl acetal → 1-(3-bromophenyl)-1,3-dihydro-2H-imidazol-2-one

HRID 70296

반응식

HRID 70296 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([N:8]=[C:9]=[O:10])[CH:3]=1.CO[CH:13](OC)[CH2:14][NH2:15]>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([N:8]2[CH:13]=[CH:14][NH:15][C:9]2=[O:10])[CH:5]=[CH:6][CH:7]=1

참가 물질

4

실험 절차

A solution of 1-bromo-3-isocyanatobenzene (1.0 mL, 8.01 mmol) and [2,2-bis(methyloxy)ethyl]amine (0.86 mL, 8.01 mmol) in CH2Cl2 (15 mL) was stirred at room temperature for 16 hr. The solution was concentrated in vacuo and the residue taken up in a mixture of CH3CN (10 mL) and H2O (3 mL). TFA (3 mL) was added and the solution stirred at room temperature for 4 hr. The solution was concentrated in vacuo, the residue taken up in EtOAc then washed with satd NaHCO3, H2O, and brine. The organics were then dried over Na2SO4, concentrated in vacuo and the residue recrystallized from EtOAc to give 1-(3-bromophenyl)-1,3-dihydro-2H-imidazol-2-one as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 6.60 (d, J=3.0 Hz, 1H), 7.03 (d, J=3.0 Hz, 1H), 7.34-7.36 (m, 2H); 7.70-7.72 (m, 1H), 8.06 (s, 1H), 10.39 (br s, 1H).

후처리

  1. concentrationThe solution was concentrated in vacuo
  2. additionthe residue taken up in a mixture of CH3CN (10 mL) and H2O (3 mL)
  3. additionTFA (3 mL) was added
  4. concentrationThe solution was concentrated in vacuo
  5. washthen washed with satd NaHCO3, H2O, and brine
  6. dry with materialThe organics were then dried over Na2SO4
  7. concentrationconcentrated in vacuo
  8. customthe residue recrystallized from EtOAc

출처 및 근거

ORD 기록
ord-49cfa41c1b5744d8b42a6de6d0d382f0
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08822518B2

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