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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736425Generated: November 4, 2026

5,5-Dibromobarbituric acid → HCID 19432920, compound

https://huagongshe.com/reaction/1736425

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,5-Dibromobarbituric acidHCID 94877—
Reactant1-(6-Chloropyridin-3-yl)ethan-1-oneHCID 2779698—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 19432920HCID 19432920126%

Reaction Steps

A solution of 784 mg of 2-chloro-5-acetylpyridine in 10 mL of THF was added via canula to a solution of 1.44 g of dibromobarbituric acid (DBBA) in 10 mL of THF. The resultant solution was heated at 50°-55° C. for 12 h, and then an additional 0.72 g DBBA was added. After stirring at 50°-55° C. for 2.5 more hours, 0.36 g DBBA was added. The mixture was allowed to stir for 2 h at which point NMR analysis of an aliquot indicated 87% conversion. The reaction mixture was cooled, diluted with ethyl acetate, washed with two portions of saturated aqueous sodium bicarbonate, water, and brine, dried over magnesium sulfate and concentrated. Purification by flash chromatography (silica gel, 15% ethyl acetate/hexane) provided 0.86 g (73%) of the title compound as a white solid: 1H NMR (400 MHz, CDCl3) δ8.96 (d, 1H, J=2.6 Hz), 8.21 (dd, 1H, J=2.5, 8.3 Hz), 7.46 (d, 1H, J=8.4 Hz), 4.37 (s, 2H). The NMR also indicated the presence of the corresponding 2-bromo derivative. The ~4:1 mixture was carried on through the synthesis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541197
Source datasetuspto-grants-1996_07
ORD IDord-98e77fef8b87447b993fb007bea1a9b5
Source noteuspto-grants-1996_07