Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038970Generated: November 2, 2026

Hydrochloric Acid → HCID 58443073, compound

https://huagongshe.com/reaction/1038970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant6-Oxo-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl esterHCID 96347—
Reactant4-(Bromomethyl)-1,2-difluorobenzeneHCID 581436—
SolventDimethylformamideHCID 6228—
ProductHCID 58443073HCID 58443073—

Reaction Steps

A mixture of sodium hydride (0.262 g, 6.54 mmol, 60% dispersion in mineral oil) and ethyl 6-oxo-1,6-dihydropyrimidine-5-carboxylate (1 g, 5.95 mmol) was dissolved in DMF (11.89 ml). After 30 min at room temperature, 3,4-difluorobenzyl bromide (0.761 ml, 5.95 mmol) was added. The reaction mixture was stirred at room temperature overnight and then poured into aqueous hydrochloric acid (10%). The aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with ethyl acetate/hexanes, to afford ethyl 1-(3,4-difluorobenzyl)-6-oxo-1,6-dihydropyrimidine-5-carboxylate as an off-white solid. LRMS (EST) calc'd for (C14H13F2N2O3) [M+H]+, 295.1; found 295.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552019B2
Source datasetuspto-grants-2013_10
ORD IDord-5af24e96ab9d48f8b1ba78f6d0953e9f
Source noteuspto-grants-2013_10