4-Bromo-6-(4-methyl-1-piperazinyl)-9-methyl-1,2-dihydrobenzo[b]-pyrrolo [3,2,1-jk][1,4]benzodiazepine → 4-Bromo-6-(4-methyl-1-piperazinyl)-9-methylbenzo[b]pyrrolo-[3,2,1-jk][1,4]benzodiazepine

HRID 35133

反応式

HRID 35133 の反応式
[Br:1][C:2]1[CH:3]=[C:4]2[CH2:13][CH2:12][N:11]3[C:5]2=[C:6]([CH:26]=1)[C:7]([N:19]1[CH2:24][CH2:23][N:22]([CH3:25])[CH2:21][CH2:20]1)=[N:8][C:9]1[CH:17]=[C:16]([CH3:18])[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:26]=1)[C:7]([N:19]1[CH2:24][CH2:23][N:22]([CH3:25])[CH2:21][CH2:20]1)=[N:8][C:9]1[CH:17]=[C:16]([CH3:18])[CH:15]=[CH:14][C:10]=13

参加物

4

実験手順

To a solution of 4-bromo-6-(4-methyl-1-piperazinyl)-9 -methyl-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine (5.7 g, 13.8 mmoles) in chloroform (540 ml) was added manganese dioxide (25 gm), and the mixture was heated under reflux for 40 days. The mixture was filtered, and the filter cake washed with dichloromethane. The filtrate was concentrated under vacuum.

後処理

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 40 days
  3. filtrationThe mixture was filtered
  4. washthe filter cake washed with dichloromethane
  5. concentrationThe filtrate was concentrated under vacuum

出典と根拠

ORDレコード
ord-61b91ee252014689baa77b43a53f2a41
出典データセット
uspto-grants-1988_08
特許番号
US04764616

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