4-Bromo-6-(4-methyl-1-piperazinyl)-1,2dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine → 4-Bromo-6-(4-methyl-1-piperazinyl)benzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine

HRID 34360노트

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HRID 34360 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[CH2:13][CH2:12][N:11]3[C:5]2=[C:6]([CH:25]=1)[C:7]([N:18]1[CH2:23][CH2:22][N:21]([CH3:24])[CH2:20][CH2:19]1)=[N:8][C:9]1[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=13>C(Cl)(Cl)Cl.[O-2].[O-2].[Mn+4]>[Br:1][C:2]1[CH:3]=[C:4]2[CH:13]=[CH:12][N:11]3[C:5]2=[C:6]([CH:25]=1)[C:7]([N:18]1[CH2:23][CH2:22][N:21]([CH3:24])[CH2:20][CH2:19]1)=[N:8][C:9]1[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=13

참가 물질

4

실험 절차

To a solution of 4-bromo-6-(4-methyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine (5.7 g, 14.3 mmoles) in chloroform (100 ml) was added manganese dioxide (5 g) and the mixture was heated at gentle reflux for 24 hours. Additional manganese dioxide was added and reflux was continued for 36 hours. The mixture was filtered and the solids were washed with dichloromethane. The filtrate was concentrated at reduced pressure. The residue was purified on a silica gel column (160 g), eluted with a mixture of methanol and dichloromethane (1.5% methanol in dichloromethane, 4 1, 2% methanol in dichloromethane, 2 1). The fractions containing pure product were combined and concentrated to give 3.7 g (64%) of product. Recrystallization from toluene (23 ml) yielded the analytical sample, mp 157°-159° C.

후처리

  1. temperaturethe mixture was heated
  2. temperatureat gentle reflux for 24 hours
  3. temperaturereflux
  4. filtrationThe mixture was filtered
  5. washthe solids were washed with dichloromethane
  6. concentrationThe filtrate was concentrated at reduced pressure
  7. customThe residue was purified on a silica gel column (160 g)
  8. washeluted with a mixture of methanol and dichloromethane (1.5% methanol in dichloromethane, 4 1, 2% methanol in dichloromethane, 2 1)
  9. additionThe fractions containing pure product
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-62d570b0b51f476594c5e814e8fd41af
출처 데이터셋
uspto-grants-1988_08
특허 번호
US04761412

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