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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479466Generated: October 31, 2026

3-(1-benzylpiperidin-4-yl)-4-(4-chlorophenyl)-3,4-dihydro-2(1H)-quinazolinone → 3-(piperidin-4-yl)-4-(4-chlorophenyl)-3,4-dihydro-2(1H)-quinazolinone

https://huagongshe.com/reaction/479466

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1-benzylpiperidin-4-yl)-4-(4-chlorophenyl)-3,4-dihydro-2(1H)-quinazolinoneHCID 12109389—
SolventDichloromethaneHCID 6344—
Solvent1-Chloroethyl chloroformateHCID 521305—
Product3-(piperidin-4-yl)-4-(4-chlorophenyl)-3,4-dihydro-2(1H)-quinazolinoneHCID 1877089197.2%

Reaction Steps

To a solution of 1.40 g (3.25 mmol) of 3-(1-benzylpiperidin-4-yl)-4-(4-chlorophenyl)-3,4-dihydro-2(1H)-quinazolinone in methylene chloride, α-chloroethyl chloroformate was added dropwise under ice-cooling and stirred for one hour. After concentration under reduced pressure, the residue was dissolved with 28 ml of methanol and stirred at room temperature for 2 hours and under ice-cooling for one hour. The precipitated crystals were collected to give 1.08 g (3.16 mmol) of the title compound as colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06645971B1
Source datasetuspto-grants-2003_11
ORD IDord-e991532bd08849448ed1659524cad056
Source noteuspto-grants-2003_11