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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455956Generated: November 2, 2026

Allyl bromide → HCID 22105593, compound

https://huagongshe.com/reaction/1455956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium CarbonateHCID 10340—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 22105683HCID 22105683—
SolventDimethylformamideHCID 6228—
ProductHCID 22105593HCID 22105593—

Reaction Steps

A mixture of ethyl 6-[2-benzyloxy-5-bromobenzylamino]-2-oxo-1,2-dihydropyridine-3-carboxylate (2.78 g), sodium carbonate (0.97 g) and allyl bromide (0.77 ml) in DMF (10 ml) was stirred for 5 days, poured into saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic solution was washed with HCl solution, saturated aqueous sodium hydrogen carbonate and brine, dried (Na2SO4), filtered and evaporated. The residue was purified by chromatography, eluting with 2.5% ethyl acetate/dichloromethane, to give ethyl 6-[2-benzyloxy-5-bromobenzylamino]-2-allyloxypyridine-3-carboxylate (1.99 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843942
Source datasetuspto-grants-1998_12
ORD IDord-1190898aa0854fcd94fc638107d6c8fe
Source noteuspto-grants-1998_12