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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530428Generated: October 31, 2026

Triethylamine → 1-{2-[(3-Aminophenyl)ethynyl]phenyl}urea

https://huagongshe.com/reaction/530428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantBenzenamine, 3-ethynyl-HCID 104682—
ReactantUrea, (2-iodophenyl)-HCID 139387—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-{2-[(3-Aminophenyl)ethynyl]phenyl}ureaHCID 121254629—

Reaction Steps

To the nitrogen degassed solution of 1-(2-iodophenyl)urea (1.31 g, 5 mmol, 1 eq), 3-ethynylaniline (0.8 mL, 1.5 eq), triphenylphosphine (32.8 mg, 0.025 eq), and triethylamine (2.1 mL, 3 eq) in anhydrous DMF (12.5 mL) was added copper(I) iodide (190.4 mg, 0.2 eq) and bis(triphenylphosphine)palladium(II) dichloride (351 mg, 0.1 eq). After the reaction mixture was stirred at room temperature for 10 minutes, it was diluted with ethyl acetate, washed sequentially with aqueous ammonium chloride, saturated aqueous sodium bicarbonate, brine, and lastly dried with anhydrous sodium sulfate. The upper solution was decanted, concentrated, and the solid mixture was subject to a gradient column chromatography (EtOAc-Hex 1:2 to MeOH-EtOAc 1:9) to give 1-{2-[(3-aminophenyl)ethynyl]phenyl}urea as a brown solid in amount of 1.26 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353093B2
Source datasetuspto-grants-2016_05
ORD IDord-04637a0d363e4c53acfb0a02963fd6b2
Source noteuspto-grants-2016_05