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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35133Generated: October 26, 2026

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/reaction/35133

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-6-(4-methyl-1-piperazinyl)-9-methyl-1,2-dihydrobenzo[b]-pyrrolo [3,2,1-jk][1,4]benzodiazepineHCID 13823314—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product4-Bromo-6-(4-methyl-1-piperazinyl)-9-methylbenzo[b]pyrrolo-[3,2,1-jk][1,4]benzodiazepineHCID 13823308—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764616
Source datasetuspto-grants-1988_08
ORD IDord-61b91ee252014689baa77b43a53f2a41
Source noteuspto-grants-1988_08