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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010318Generated: October 30, 2026

4-Fluorophenyl isocyanate → N-(4-{2-[(Cyclopropylmethyl)aminocarbonyl]pyridin-4-yl}oxyphenyl)-N'-(4-fluorophenyl)urea

https://huagongshe.com/reaction/1010318

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorophenyl isocyanateHCID 70955—
Reactant4-(4-Aminophenoxy)-N-(cyclopropylmethyl)picolinamideHCID 58931153—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-{2-[(Cyclopropylmethyl)aminocarbonyl]pyridin-4-yl}oxyphenyl)-N'-(4-fluorophenyl)ureaHCID 58930960—

Reaction Steps

After adding 100 mg of 4-(4-Aminophenoxy)-2-[(cyclopropylmethyl)aminocarbonyl]pyridine to 5 ml of tetrahydrofuran, 0.075 ml of p-fluorophenyl isocyanate was added at room temperature and the mixture was stirred for 1 hour. NH type silica gel was added to the reaction solution, the solvent was distilled off under reduced pressure and the reaction product was adsorbed onto the silica gel. The silica gel was charged into a dry column packed with NH type silica gel, and column purification was performed (hexane:ethyl acetate=1:1, followed by ethyl acetate and ethyl acetate:methanol=10:1). The solvent was distilled off under reduced pressure, ethyl acetate and hexane were added to the residue, and the precipitated solid was filtered out to obtain 25 mg of the target substance as a light yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973160B2
Source datasetuspto-grants-2011_07
ORD IDord-c06b3bfda0bb48d4b8cd525dbe78273f
Source noteuspto-grants-2011_07