반응식
[Cl: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]>[Cl: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]=13참가 물질
4
실험 절차
To a solution of 4-chloro-6-(4-methyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine (6 g, 17 mmoles), in chloroform (150 ml) was added manganese dioxide (10.5 g). The mixture was heated under reflux for 24 hours. The mixture was cooled, filtered and the solid was washed with dichloromethane (200 ml). The filtrate was then concentrated to dryness. The residue was purified by flash chromatography over a silica gel column (150 g), eluted with 2% methanol in dichloromethane (4 l) and 3% methanol in dichloromethane (2 l). Evaporation of the eluent gave 3.8 g (63%) of product. Recrystallization from toluene (40 ml) yielded the analytical sample, mp 170°-172° C.
후처리
- temperatureThe mixture was heated
- temperatureunder reflux for 24 hours
- temperatureThe mixture was cooled
- filtrationfiltered
- washthe solid was washed with dichloromethane (200 ml)
- concentrationThe filtrate was then concentrated to dryness
- customThe residue was purified by flash chromatography over a silica gel column (150 g)
- washeluted with 2% methanol in dichloromethane (4 l) and 3% methanol in dichloromethane (2 l)
- customEvaporation of the eluent
출처 및 근거
- ORD 기록
- ord-e9900028a3e64abb947a008cb915a7e1
- 출처 데이터셋
- uspto-grants-1988_02
- 특허 번호
- US04723003
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