1,4-Diiodobutane → (4aRS,5SR,8aRS)-1-benzyl-5-(pyrrolidin-1-yl)perhydroquinoxaline-2,3-dione

HRID 1876800

반응식

HRID 1876800 반응식
[NH2:1][CH:2]1[CH2:11][CH2:10][CH2:9][CH:8]2[CH:3]1[NH:4][C:5](=[O:20])[C:6](=[O:19])[N:7]2[CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C([O-])(O)=O.[Na+].I[CH2:27][CH2:28][CH2:29][CH2:30]I>CC#N>[CH2:12]([N:7]1[CH:8]2[CH:3]([CH:2]([N:1]3[CH2:30][CH2:29][CH2:28][CH2:27]3)[CH2:11][CH2:10][CH2:9]2)[NH:4][C:5](=[O:20])[C:6]1=[O:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

참가 물질

5

실험 절차

(4aRS,5SR,8aRS)-5-Amino-1-benzylperhydroquinoxaline-2,3-dione (3.06 g, 11.2 mmol) was dissolved in CH3CN (300 ml). NaHCO3 (6.4 g, 76.2 mmol) and 1,4-diiodobutane (13.9 g, 44.8 mmol, 5.9 ml) were added and the mixture was heated under reflux for 18 hours. NaHCO3 was separated off with a blue-band filter (Schleicher&Schuell) and the yellow solution was concentrated in vacuo. The solid was taken up in CH2Cl2 and the mixture was extracted by shaking three times with HCl (1 N). The aqueous phase was then brought to pH 8 with NaOH (2 N) and extracted by shaking three times with CH2Cl2. The organic phases were dried over Na2SO4 and evaporated in vacuo. A pale yellow solid was obtained.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 18 hours
  3. customNaHCO3 was separated off with a blue-band filter (Schleicher&Schuell)
  4. concentrationthe yellow solution was concentrated in vacuo
  5. extractionthe mixture was extracted
  6. extractionextracted
  7. stirringby shaking three times with CH2Cl2
  8. dry with materialThe organic phases were dried over Na2SO4
  9. customevaporated in vacuo
  10. customA pale yellow solid was obtained

출처 및 근거

ORD 기록
ord-f8523a2b440a489c84e2be6a3be9cf77
출처 데이터셋
uspto-grants-2012_11
특허 번호
US08309725B2

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