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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64409Generated: October 25, 2026

Bromoacetone → HCID 86713417, compound

https://huagongshe.com/reaction/64409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetoneHCID 11715—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 6-amino-5-[(2-fluorobenzyl)oxy]nicotinateHCID 86713416—
SolventEthanolHCID 702—
ProductHCID 86713417HCID 86713417—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 2.15 g of methyl 6-amino-5-[(2-fluorobenzyl)oxy]nicotinate in 43 ml of ethanol was added 1.09 ml of bromoacetone, followed by stirring at 80° C. for 4 hours. To the reaction mixture was added 1.09 ml of bromoacetone, followed by stirring at 80° C. for 4 hours. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution, and the solvent was evaporated under reduced pressure, followed by extracting with ethyl acetate and washing with saturated brine. After drying over anhydrous magnesium sulfate and then filtering, the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 1.39 g of methyl 8-[(2-fluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridine-6-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447090B2
Source datasetuspto-grants-2016_09
ORD IDord-2d92678427e44e14afb990b87d1e5427
Source noteuspto-grants-2016_09