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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026313Generated: October 31, 2026

2-Bromo-1-(4-hydroxyphenyl)ethanone → 4-[6-(Cyclopropylmethoxy)imidazo[1,2-a]pyridin-2-yl]phenol

https://huagongshe.com/reaction/1026313

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(4-hydroxyphenyl)ethanoneHCID 4964—
Reactant5-(Cyclopropylmethoxy)pyridin-2-amineHCID 28413660—
SolventEthanolHCID 702—
Product4-[6-(Cyclopropylmethoxy)imidazo[1,2-a]pyridin-2-yl]phenolHCID 67778202100.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-(cyclopropylmethoxy)pyridin-2-amine (328 mg), 2-bromo-1-(4-hydroxyphenyl)ethanone (430 mg) and ethanol (10 mL) was stirred at 80° C. for 4 hr. The reaction mixture was allowed to cool to room temperature, and the resulting crystals were collected by filtration. The obtained crystals were dissolved in saturated aqueous sodium hydrogen carbonate solution and THF, and the solution was extracted twice with ethyl acetate. The combined organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound as a brown solid (561 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729102B2
Source datasetuspto-grants-2014_05
ORD IDord-36e985b3248a49219b2ac22179955b48
Source noteuspto-grants-2014_05