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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890754Generated: October 31, 2026

Phosphorus oxybromide → 5-Bromo-1,2,3,4-tetrahydro-2-(phenylmethyl)-2,6-naphthyridine

https://huagongshe.com/reaction/1890754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxybromideHCID 24613—
ReactantSodium BicarbonateHCID 516892—
Reactant6-benzyl-5,6,7,8-tetrahydro-2,6-naphthyridin-1(2H)-oneHCID 22335190—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventAnisoleHCID 7519—
Product5-Bromo-1,2,3,4-tetrahydro-2-(phenylmethyl)-2,6-naphthyridineHCID 22335402—

Reaction Steps

Phosphorous oxybromide (7.5 g, 26 mmol) is added portion wise to a suspension of 6-benzyl-5,6,7,8-tetrahydro-2,6-naphthyridin-1(2H)-one (1.6 g, 6.7 mmol) in anisole (20 mL) and acetonitrile (10 mL). The reaction mixture is stirred under reflux for 4 hours. The cooled mixture is poured onto ice and diluted with dichloromethane. The mixture is slowly neutralized using saturated sodium bicarbonate solution. The aqueous phase is extracted with dichloromethane three times. The organic phase are combined and washed with brine, dried over Na2SO4 and taken to dryness by rotary evaporation. The crude product as purified by column chromatography on silica gel to afford 2-benzyl-5-bromo-1,2,3,4-tetrahydro-2,6-naphthyridine as a white solid. MS m/z 303.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507491B2
Source datasetuspto-grants-2013_08
ORD IDord-1750751994044f53bc7af08940a1b7be
Source noteuspto-grants-2013_08