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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809198Generated: November 1, 2026

N-bromobutanimide → 3,6,8-Tribromoimidazo[1,2-a]pyrazine

https://huagongshe.com/reaction/1809198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant6,8-Dibromoimidazo[1,2-a]pyrazineHCID 15025843—
SolventDichloromethaneHCID 6344—
Product3,6,8-Tribromoimidazo[1,2-a]pyrazineHCID 14207622—

Reaction Steps

N-bromosuccinimide (1.81 g, 10.15 mmol) was added to a solution of 6,8-Dibromo-imidazo[1,2-a]pyrazine (2.0 g, 10.15 mmol) in dichloromethane (40 ml). The reaction was stirred at room temperature over night then diluted with dichloromethane (100 ml) and washed with saturated aqueous sodium hydrogen carbonate (2×50 ml) and brine (50 ml). The organic layer was dried (MgSO4), filtered and concentrated in vaccuo. The product, 3,6,8-Tribromo-imidazo[1,2-a]pyrazine was obtained as a pink solid (2.77 g), sufficiently pure to be used in subsequent reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362018B2
Source datasetuspto-grants-2013_01
ORD IDord-0fb4b0376bbf47478e875a3846773a01
Source noteuspto-grants-2013_01