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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230303Generated: October 25, 2026

Iodoethane → N-(4-iodophenyl)-N-ethylpyrimidin-2-amine

https://huagongshe.com/reaction/230303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantN-(4-iodophenyl)pyrimidin-2-amineHCID 57762548—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductN-(4-iodophenyl)-N-ethylpyrimidin-2-amineHCID 57762566—

Reaction Steps

Under an argon atmosphere, a solution of N-(4-iodophenyl)pyrimidin-2-amine (255 mg) in anhydrous DMF (1 ml) was added dropwise to a suspension of sodium hydride (40 mg) in anhydrous DMF (1 ml), and the resulting mixture was stirred at room temperature for 75 minutes. Ethyl iodide (0.10 ml) was added dropwise to the reaction solution and the resulting mixture was stirred at room temperature overnight. Saturated brine was added thereto and the resulting mixture was extracted with chloroform. Organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by column chromatography (silica gel, eluent: cyclohexane/chloroform=1/10) to obtain N-(4-iodophenyl)-N-ethylpyrimidin-2-amine (264 mg). NMR (H1, CDCl3): δ 1.23(3H, t, J=6.8 Hz), 4.01 (2H, q, J=6.8 Hz), 6.57 (1H, t, J=4.9 Hz), 7.03-7.06 (2H, m), 7.70-7.74 (2H, m), 8.32 (2H, d, J=4.9 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566724B2
Source datasetuspto-grants-2009_07
ORD IDord-063b57cd3e9c4354a82207246c7d1a86
Source noteuspto-grants-2009_07