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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156355Generated: October 31, 2026

Potassium Iodide → 1-[3-[4-(4-fluorobenzoyl)-1-piperidinyl]propyl]-2,3-dihydro-2,2-dimethyl-4(1H)-quinazolinone

https://huagongshe.com/reaction/1156355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactantp-Fluorophenyl 4-piperidyl ketone hydrochlorideHCID 3084438—
Reactant1-(3-chloropropyl)-2,3-dihydro-2,2-dimethyl-4(1H)-quinazolinoneHCID 20278942—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
Product1-[3-[4-(4-fluorobenzoyl)-1-piperidinyl]propyl]-2,3-dihydro-2,2-dimethyl-4(1H)-quinazolinoneHCID 1285206778%

Reaction Steps

A mixture of 5.6 parts of 1-(3-chloropropyl)-2,3-dihydro-2,2-dimethyl-4(1H)-quinazolinone, 4.9 parts of (4-fluorophenyl) (4-piperidinyl)methanone hydrochloride, 10 parts of sodium carbonate, 0.1 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed overnight with water-separator. The reaction mixture is cooled, water is added and the layers are separated. The 4-methyl-2-pentanone phase is dried, filtered and evaporated. The solid 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 solid residue is stirred in 2,2'-oxybispropane. The product is filtered off and dried, yielding 6.6 parts (78%) of 1-[3-[4-(4-fluorobenzoyl)-1-piperidinyl]propyl]-2,3-dihydro-2,2-dimethyl-4(1H)-quinazolinone; mp. 185.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04335127
Source datasetuspto-grants-1982_06
ORD IDord-2c86ee42cc654b87abe799a80b9d805a
Source noteuspto-grants-1982_06