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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75665Generated: October 29, 2026

Methylamine → 1-(2-Fluoro-4-iodophenyl)-3-methylurea

https://huagongshe.com/reaction/75665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-Fluoro-4-iodoanilineHCID 185694—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventToluene waterHCID 22272177—
Product1-(2-Fluoro-4-iodophenyl)-3-methylureaHCID 5971735194.8%

Reaction Steps

Under a nitrogen atmosphere, to N,N-carbonyldiimidazole (61.4 g) were added N,N-dimethylformamide (300 ml) and triethylamine (52.8 ml) and a solution of 2-fluoro-4-iodoaniline 47 (74.8 g) in N,N-dimethylformamide (75 ml) was added dropwise with stirring 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 a solution (60 ml) of 40% methylamine in methanol 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), 1125 ml] under stirring. The precipitated crystals were collected by filtration and dried to give 1-(2-fluoro-4-iodophenyl)-3-methylurea 63 (87.9 g, yield 94.8%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835443B2
Source datasetuspto-grants-2014_09
ORD IDord-9f5faabee287429ebdb6145a23e54304
Source noteuspto-grants-2014_09