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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224166Generated: October 27, 2026

Triethylamine → N-Cyclopropyl-N'-(2-fluoro-4-iodophenyl)urea

https://huagongshe.com/reaction/2224166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantCyclopropylamineHCID 69828—
Reactant2-Fluoro-4-iodoanilineHCID 185694—
SolventDimethylformamideHCID 6228—
SolventToluene waterHCID 22272177—
ProductN-Cyclopropyl-N'-(2-fluoro-4-iodophenyl)ureaHCID 5971705495.5%

Reaction Steps

Under a nitrogen atmosphere, to N,N-carbonyldiimidazole (82.1 g) were added N,N-dimethylformamide (400 ml) and triethylamine (70.5 ml), and a solution of 2-fluoro-4-iodoaniline 47 (100 g) in N,N-dimethylformamide (100 ml) was added dropwise under ice-cooling. After the completion of the dropwise addition, the mixture was stirred at room temperature for 5 hrs. The reaction mixture was ice-cooled, and cyclopropylamine (44.0 ml) was added dropwise. The mixture was stirred at room temperature for 1 hr, and the reaction mixture was added dropwise to water-toluene [2:1 (volume ratio), 1500 ml] with stirring. The precipitated crystals were collected by filtration and dried to give 1-cyclopropyl-3-(2-fluoro-4-iodo-phenyl)-urea 48 (129 g, yield 95.5%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378423B2
Source datasetuspto-grants-2008_05
ORD IDord-e3c62755c0eb47b8b861e2fd50a5351e
Source noteuspto-grants-2008_05