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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478217Generated: October 31, 2026

Bromine → 3-Bromo-7-methylimidazo[1,2-a]pyrimidine

https://huagongshe.com/reaction/478217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantPotassium BromideHCID 253877—
ReactantSodium AcetateHCID 517045—
Reactant7-Methylimidazo[1,2-a]pyrimidineHCID 11332492—
SolventMethanolHCID 887—
Product3-Bromo-7-methylimidazo[1,2-a]pyrimidineHCID 1140158363%

Reaction Steps

7-Methylimidazo[1,2-a]pyrimidine (100 mg, 0.75 mmol) and sodium acetate (74 mg, 0.90 mmol) were dissolved in methanol (2 ml) which had been saturated with potassium bromide and this mixture was cooled to −10° C. before dropwise addition of bromine (132 mg, 0.83 mmol) over 5 min. On complete addition the mixture was quenched by addition of 1M sodium sulfite solution (2 ml) and the solvent removed in vacuo. The residue was treated with water (15 ml) and saturated sodium hydrogencarbonate solution (15 ml) and extracted with ethyl acetate (3×40 ml). The organics were combined then washed with brine (40 ml), dried over anhydrous sodium sulfate and evaporated to give an off white solid. This solid was purified by silica gel chromatography eluting with dichloromethane and 1% conc. ammonia on a gradient of methanol (1-2%) to give 3-bromo-7-methylimidazo[1,2-a]pyrimidine (100 mg, 63%) as a white crystalline solid: δH (400 MHz, CDCl3) 2.67 (3H, s), 6.87 (1H, d, J 7), 7.71 (1H, s), 8.27 (1H, d, J 7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642229B2
Source datasetuspto-grants-2003_11
ORD IDord-75fdc91a0f444d2191ac6562ef89bd33
Source noteuspto-grants-2003_11