3-Bromoaniline → 1-(3-Bromophenyl)imidazolidin-2-one

HRID 471833노트

반응식

HRID 471833 반응식
Cl[CH2:2][CH2:3][N:4]=[C:5]=[O:6].[Br:7][C:8]1[CH:9]=[C:10]([CH:12]=[CH:13][CH:14]=1)[NH2:11].[H-].[Na+]>CN(C=O)C.CCOC(C)=O>[Br:7][C:8]1[CH:9]=[C:10]([N:11]2[CH2:2][CH2:3][NH:4][C:5]2=[O:6])[CH:12]=[CH:13][CH:14]=1

참가 물질

6

실험 절차

1-Chloro-2-isocyanatoethane (1.18 mL, 13.8 mmol) was added dropwise to a solution of 3-bromoaniline (1.5 mL, 13.8 mmol) in DMF (30 mL) at 0° C. then stirred at room temperature for 16 hr, then 70° C. for 2 hr. The solution was cooled to room temperature and 1-chloro-2-isocyanatoethane (0.40 mL, 4.69 mmol) was added. After stirring at room temperature for 2 hr, the solution was diluted with DMF (120 mL), cooled to 0° C. and NaH (660 mg, 60% dispersion in mineral oil, 16.5 mmol) added in portions. The mixture was stirred at room temperature for 64 hr, then diluted with EtOAc. After washing with H2O three times then brine the solution was dried over Na2SO4, concentrated in vacuo and the residue purified by silica gel chromatography (EtOAc/hexanes) to give 1-(3-bromophenyl)-2-imidazolidinone as a white solid. 1H NMR (400 MHz, CDCl3) δ ppm 3.56-3.62 (m, 2H), 3.88-3.92 (m, 2H), 5.20 (br s, 1H), 7.15-7.20 (m, 2H), 7.49-7.51 (m, 1H), 7.71 (s, 1H).

후처리

  1. wait70° C. for 2 hr
  2. temperatureThe solution was cooled to room temperature
  3. stirringAfter stirring at room temperature for 2 hr
  4. temperaturecooled to 0° C.
  5. stirringThe mixture was stirred at room temperature for 64 hr
  6. washAfter washing with H2O three times
  7. dry with materialbrine the solution was dried over Na2SO4
  8. concentrationconcentrated in vacuo
  9. customthe residue purified by silica gel chromatography (EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-795b3254696b4eaf8ab32480b2f3295b
출처 데이터셋
uspto-grants-2014_01
특허 번호
US08633175B2

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