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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571050Generated: October 31, 2026

N-Bromosuccinamide → 3-(benzyloxy)-1-(biphenyl-3-yl)-5-bromopyridin-4(1H)-one

https://huagongshe.com/reaction/571050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BromosuccinamideHCID 9834204—
Reactant3-(benzyloxy)-1-(biphenyl-3-yl)pyridin-4(1H)-oneHCID 67418143—
SolventAcetic AcidHCID 176—
Product3-(benzyloxy)-1-(biphenyl-3-yl)-5-bromopyridin-4(1H)-oneHCID 67420197—

Reaction Steps

To a solution of 3-(benzyloxy)-1-(biphenyl-3-yl)pyridin-4(1H)-one (2.41 g, 6.8 mmol) in AcOH (68 mL) was added N-bromosuccinamide (2.67 g, 15 mmol) and the reaction mixture was stirred at room temperature. After 1 h, the mixture was concentrated under reduced pressure and purified by flash chromatography (80 g SiO2, 0-100% ethyl acetate/hexanes) to provide 3-(benzyloxy)-1-(biphenyl-3-yl)-5-bromopyridin-4(1H)-one. LC/MS (M+H)+ 432/434.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024032B2
Source datasetuspto-grants-2015_05
ORD IDord-fb7072b6dfc2433f8f16a82eba73b744
Source noteuspto-grants-2015_05