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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75648Generated: October 27, 2026

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

https://huagongshe.com/reaction/75648

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 5971705493.4%

Reaction Steps

Under a nitrogen atmosphere, to N,N-carbonyldiimidazole (39.9 g) were added N,N-dimethylformamide (200 ml) and triethylamine (34.3 ml) and a solution of 2-fluoro-4-iodoaniline 47 (48.5 g) in N,N-dimethylformamide (50 ml) was added dropwise with stirring under ice-cooling. After the completion of the dropwise addition, the mixture was stirred at room temperature for 18 hrs. The reaction mixture was ice-cooled, and cyclopropylamine (21.3 ml) was added dropwise. The reaction mixture was stirred at room temperature for 1 hr and added dropwise to water-toluene [2:1 (volume ratio), 750 ml] with stirring. The precipitated crystals were collected by filtration and dried to give 1-cyclopropyl-3-(2-fluoro-4-iodophenyl)urea 48 (61.3 g, yield 93.4%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835443B2
Source datasetuspto-grants-2014_09
ORD IDord-b83af1a5c8c745d3acecb5894ea8008b
Source noteuspto-grants-2014_09