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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49783Generated: October 26, 2026

4-Fluorophenyl isocyanate → N-(1-acetylpiperidin-4-yl)-N'-(4-fluorophenyl)urea

https://huagongshe.com/reaction/49783

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorophenyl isocyanateHCID 70955—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Acetyl-4-aminopiperidine hydrochlorideHCID 17221642—
SolventDichloromethaneHCID 6344—
ProductN-(1-acetylpiperidin-4-yl)-N'-(4-fluorophenyl)ureaHCID 9860476—

Reaction Steps

To a suspension of 1-acetyl-4-aminopiperidine hydrochloride (536 mg) in dichloromethane (5 ml) were added 4-fluorophenyl isocyanate (375 μl) and diisopropylethylamine (575 μl ) at ambient temperature. After stirring for 3 hours, the reaction mixture was diluted with dichloromethane. An organic phase was separated and an aqueous phase was extracted with dichloromethane. A combined organic phase was dried over magnesium sulfate and the solvents were removed under reduced pressure. After crystallization from diisopropyl ether and n-hexane, N-(1-acetylpiperidin-4-yl)-N′-(4-fluorophenyl)urea (448 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710043B1
Source datasetuspto-grants-2004_03
ORD IDord-791c61bd4d46488d9cd3f88bc69b7774
Source noteuspto-grants-2004_03