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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752057Generated: October 28, 2026

3-Bromopropionitrile → HCID 57762584, compound

https://huagongshe.com/reaction/1752057

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopropionitrileHCID 17020—
ReactantSodium hydrideHCID 24758—
ReactantN-(4-iodophenyl)pyrimidin-2-amineHCID 57762548—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 57762584HCID 57762584—

Reaction Steps

Under an argon atmosphere, a solution of N-(4-iodophenyl)pyrimidin-2-amine (100 mg) in anhydrous DMF (1.0 ml) was added to a suspension of sodium hydride (16 mg) in anhydrous DMF (1.0 ml), and the resulting mixture was stirred at room temperature for 30 minutes. To the reaction solution, a solution of 3-bromopropionitrile (0.04 ml) in anhydrous DMF (0.5 ml) was added, and the resulting mixture was stirred at room temperature overnight. Saturated brine was added to the reaction solution and the resulting mixture was extracted with chloroform. Organic layer was 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: hexane/chloroform=1/10) to obtain 3-(N-(4-iodophenyl)-N-(pyrimidin-2-yl)amino)propanenitrile (94 mg). NMR (H1, CDCl3): δ 2.82 (2H, t, J=6.8 Hz), 4.24 (2H, t, J=6.8 Hz), 6.68 (1H, t, J=4.9 Hz), 7.06-7.10 (2H, m), 7.74-7.78 (2H, m), 8.35 (2H, d, J=4.9 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162988B2
Source datasetuspto-grants-2015_10
ORD IDord-7375c073eb1d4a47b67886f3b2c41a07
Source noteuspto-grants-2015_10