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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248239Generated: November 1, 2026

4-(4-Fluorobenzoyl)piperidine → HCID 12852062, compound

https://huagongshe.com/reaction/1248239

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Fluorobenzoyl)piperidineHCID 2724440—
ReactantHCID 20278944HCID 20278944—
SolventEthanolHCID 702—
ProductHCID 12852062HCID 1285206257%

Reaction Steps

A mixture of 5.8 parts of 6-chloro-3-(2-chloroethyl)-3,4-dihydro-4-phenyl-2(1H)-quinazolinone, 7.4 parts of (4-fluorophenyl)(4-piperidinyl)methanone and 56 parts of ethanol is stirred and refluxed overnight. The reaction mixture 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 oily residue solidifies on triturating in 2,2'-oxybispropane. The product is filtered off and dried, yielding 5 parts (57%) of 6-chloro-3-[2-[4-(4-fluorobenzoyl)-1-piperidinyl]ethyl]-3,4-dihydro-4-phenyl-2(1H)-quinazolinone; mp. 196° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04522945
Source datasetuspto-grants-1985_06
ORD IDord-fefdc7dddf1e44038d3dc4500bf0c18f
Source noteuspto-grants-1985_06