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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4036Generated: October 28, 2026

Dichloromethane → N-[2-(5-bromo-1-indolinyl)-5-bromophenyl]-4-methyl-1-piperazinecarboxamide

https://huagongshe.com/reaction/4036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantN-bromobutanimideHCID 67184—
ReactantN-[2-(indolin-1-yl)-5-bromophenyl]-4-methyl-1-piperazinecarboxamideHCID 13823352—
SolventDimethylformamideHCID 6228—
ProductN-[2-(5-bromo-1-indolinyl)-5-bromophenyl]-4-methyl-1-piperazinecarboxamideHCID 1382336884%

Reaction Conditions

Temperature60 °C

Reaction Steps

N-Bromosuccinimide (2.6 g, 14.5 mmoles) was added to a solution of N-[2-(indolin-1-yl)-5-bromophenyl]-4-methyl-1-piperazinecarboxamide (5.0 g, 12.0 mmoles) in dimethylformamide (50 ml). The solution was stirred at room temperature for 15 minutes and at 60° C. for 15 minutes. The solution was cooled and poured into dichloromethane (500 ml). The layers were separated and the organic phase was washed with water (3×500 ml), brine (500 ml), and dried over anhydrous sodium sulfate. The mixture was filtered and the filtrate was concentrated. The residue was purified by chromatography over silica gel (60 g, eluted with 4% methanol:96% dichloromethane, 1 l). The appropriate fractions were pooled and concentrated to give 4.8 g (84%) of product. Recrystallization from chloroform and hexane gave the analytical sample, mp 118°-119.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04723007
Source datasetuspto-grants-1988_02
ORD IDord-53391d34fae14644b538478e4ff63a6d
Source noteuspto-grants-1988_02