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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904530Generated: October 28, 2026

N-bromobutanimide → 3-Bromo-6,8-dimethylimidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/1904530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
Reactant6,8-Dimethylimidazo[1,2-b]pyridazineHCID 14750357—
SolventChloroformHCID 6212—
Product3-Bromo-6,8-dimethylimidazo[1,2-b]pyridazineHCID 1475035683.5%

Reaction Steps

To a solution of 3.63 g (24.7 mmol) of 6,8-dimethylimidazo[1,2-b]pyridazine in 25 mL of chloroform was added 4.84 g (27.2 mmol) of N-bromosuccinimide. After 2 h, 1 mL of a saturated aqueous solution of sodium bicarbonate was added. The layers were separated. The organic layer was dried (Na2SO4) and the solvent was removed with a rotary evaporator. The residue was purified by flash chromatography to give 4.66 g of the title compound as a white solid, m.p. 137°-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04838925
Source datasetuspto-grants-1989_06
ORD IDord-deac443450254f8daf47a72e6367aa4d
Source noteuspto-grants-1989_06