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HRID 35133作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/35133

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromo-6-(4-methyl-1-piperazinyl)-9-methyl-1,2-dihydrobenzo[b]-pyrrolo [3,2,1-jk][1,4]benzodiazepineHCID 13823314—
触媒HCID 178418406HCID 178418406—
溶媒ChloroformHCID 6212—
生成物4-Bromo-6-(4-methyl-1-piperazinyl)-9-methylbenzo[b]pyrrolo-[3,2,1-jk][1,4]benzodiazepineHCID 13823308—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04764616
出典データセットuspto-grants-1988_08
ORD IDord-61b91ee252014689baa77b43a53f2a41
出典メモuspto-grants-1988_08