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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277812Generated: October 26, 2026

Phenyl isocyanate → Urea, N-(2-fluoro-4-pyridinyl)-N'-phenyl-

https://huagongshe.com/reaction/1277812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
Reactant2-Fluoropyridin-4-amineHCID 2762830—
SolventBenzeneHCID 241—
ProductUrea, N-(2-fluoro-4-pyridinyl)-N'-phenyl-HCID 1289723048.9%

Reaction Steps

112 mg (1 mmol) of 2-fluoro-4-aminopyridine was added to 9 ml of dry benzene and to the resulting solution was further added 119 mg (1 mmol) of phenyl isocyanate. After stirring at room temperature for 30 hrs., the crystals which deposited were collected by filtration and then subjected to chromatography in a conventional manner using alumina. After developing the column with a benzene-ethyl acetate (3:1 by volume) solvent mixture, eluate containing the objective compound was collected. After distilling solvent off under reduced pressure, the residue was recrystallized from an ethyl acetate-n-hexane solvent mixture to give 113 mg of the objective compound: yield 48.9%; m.p. 179°-180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04279639
Source datasetuspto-grants-1981_07
ORD IDord-2b870d114b884298a85da9197f8358a7
Source noteuspto-grants-1981_07