Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617126Generated: October 30, 2026

Ethyl Acetate → 7-Hydroxy-2-(4-hydroxy-phenyl)-3-{4-[2-(piperidin-1-yl)-ethoxy]-phenyl}-3H-quinazolin-4-one

https://huagongshe.com/reaction/617126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3-[4-(2-Chloro-ethoxy)-phenyl]-7-hydroxy-2-(4-hydroxy-phenyl)-3H-quinazolin-4-oneHCID 135822830—
SolventPiperidineHCID 8082—
Product7-Hydroxy-2-(4-hydroxy-phenyl)-3-{4-[2-(piperidin-1-yl)-ethoxy]-phenyl}-3H-quinazolin-4-oneHCID 135544121—

Reaction Steps

A solution containing 0.25 g (0.000612 mol) of 3-[4-(2-chloro-ethoxy)-phenyl]-7-hydroxy-2-(4-hydroxy-phenyl)-3H-quinazolin-4-one in 7 mL of piperidine was stirred and heated to reflux for 2 hours. After cooling to room temperature, ethyl acetate was added to the reaction mixture and the solvents were co-evaporated to near dryness in a rotary evaporator. The dark residue was extracted with ethyl acetate and water. The aqueous layer was removed and chilled on ice. The precipitate which then formed was collected by vacuum filtration (0.052 g, mp 185-190° C.) and was shown to be the hydrochloride salt monohydrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05948775
Source datasetuspto-grants-1999_09
ORD IDord-9eb72418a59d4e4d8468e3a7f6857f09
Source noteuspto-grants-1999_09