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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4065Generated: October 28, 2026

N-[2-(5-bromo-1-indolinyl)phenyl]-4-methyl-1-piperazinecarboxamide → 4-Bromo-6-(4-methyl-1-piperazinyl)-1,2dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine

https://huagongshe.com/reaction/4065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[2-(5-bromo-1-indolinyl)phenyl]-4-methyl-1-piperazinecarboxamideHCID 13823366—
SolventPhosphorus oxychlorideHCID 24813—
Product4-Bromo-6-(4-methyl-1-piperazinyl)-1,2dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepineHCID 1382329457%

Reaction Steps

A mixture of N-[2-(5-bromo-1-indolinyl)phenyl]-4-methyl-1-piperazinecarboxamide (11.5 g, 27.5 mmoles) and 750 ml of phosphorus oxychloride was stirred until a solution was obtained and then heated under reflux for 40 minutes. The reaction mixture was cooled. Excess phosphorus oxychloride was removed by evaporation at 50°-55° C. The residue was dried for 30 minutes under vacuum. Ice-chilled 2N sodium hydroxide solution (250 ml) and dichloromethane (350 ml) were added to the residue at 4° C. (ice-water bath). The mixture was stirred until all the solid had dissolved. The organic phase was separated and washed with brine (2 times, 200 ml), dried over anhydrous magnesium sulfate and concentrated. Crystallization from ether (100 ml) gave 5.7 g (57%) of product. Recrystallization from isopropanol yielded the analytical sample, mp 203°-204° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04723003
Source datasetuspto-grants-1988_02
ORD IDord-5f08fd378dbe4e63866b0a1299019a73
Source noteuspto-grants-1988_02