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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156356Generated: November 1, 2026

Potassium Iodide → 3-[2-[4-(4-fluorobenzoyl)-1-piperidinyl]ethyl]-2-phenyl-4(3H)-quinazolinone

https://huagongshe.com/reaction/1156356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant3-(2-chloroethyl)-2-phenylquinazolin-4(3H)-oneHCID 2772080—
Reactantp-Fluorophenyl 4-piperidyl ketone hydrochlorideHCID 3084438—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
Product3-[2-[4-(4-fluorobenzoyl)-1-piperidinyl]ethyl]-2-phenyl-4(3H)-quinazolinoneHCID 1285206869%

Reaction Steps

A mixture of 5.5 parts of 3-(2-chloroethyl)-2-phenyl-4(3H)-quinazolinone, 4 parts of (4-fluorophenyl)(4-piperidinyl)methanone hydrochloride, 7 parts of sodium carbonate, 0.1 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 24 hours using a water-separator. The reaction mixture is filtered while hot. The filtrate is evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from a mixture of ethanol and 1,1'-oxybisethane. The product is filtered off and dried, yielding 5 parts (69%) of 3-[2-[4-(4-fluorobenzoyl)-1-piperidinyl]ethyl]-2-phenyl-4(3H)-quinazolinone; mp. 143.8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04335127
Source datasetuspto-grants-1982_06
ORD IDord-17c64b0d61264e1a84fd3c2b86ae4b03
Source noteuspto-grants-1982_06