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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71179Generated: October 30, 2026

Potassium Iodide → 6-bromo-2-methoxy-3-(4-methyl-1H-imidazol-1-yl)pyridine

https://huagongshe.com/reaction/71179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDimethylformamideHCID 6228—
ReactantChloroacetoneHCID 6571—
ReactantCesium carbonateHCID 10796—
ReactantN-(6-bromo-2-methoxypyridin-3-yl)formamideHCID 71492501—
Product6-bromo-2-methoxy-3-(4-methyl-1H-imidazol-1-yl)pyridineHCID 57609300—

Reaction Steps

To a mixture of N-(6-bromo-2-methoxypyridin-3-yl)formamide (8.0 g), cesium carbonate (20.1 g) and potassium iodide (580 mg) in DMF (40 mL) was added 1-chloropropan-2-one (4.13 mL), and the mixture was stirred at room temperature for 3 hr. The solvent was evaporated under reduced pressure, water was added, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. Acetic acid (50 mL) and ammonium acetate (26.7 g) were added to the residue, and the mixture was stirred at 130° C. for 3 hr. The reaction mixture was allowed to cool to room temperature, and the solvent was evaporated under reduced pressure. Water was added, and the mixture was neutralized with aqueous sodium hydroxide solution and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (4.72 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822699B2
Source datasetuspto-grants-2014_09
ORD IDord-c199a4d668fb4c39a80174b93f5a2aff
Source noteuspto-grants-2014_09