Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266138Generated: October 30, 2026

Ethanol → 4-(3,4-Dimethoxyphenyl)-6,7-dimethoxy-2-piperidinomethylquinazoline

https://huagongshe.com/reaction/266138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPiperidineHCID 8082—
Reactant2-Chloromethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinazolineHCID 10785656—
SolventDichloromethaneHCID 6344—
Product4-(3,4-Dimethoxyphenyl)-6,7-dimethoxy-2-piperidinomethylquinazolineHCID 2209762965%

Reaction Steps

A mixture of 2-chloromethyl-4-(3,4-dimethoxyphenyl)-6,7-dimethoxyquinazoline (2.0 g), piperidine (2.27 g) and ethanol (40 ml)--dichloromethane (10 ml) was stirred at room temperature for 3 days. The reaction mixture was concentrated under reduced pressure, and dichloromethane (50 ml) was added to the residue. The dichloromethane layer was washed with water and dried over magnesium sulfate, and the solvent was evaporated. The residue was subjected to column chromatography on silica gel. The fractions eluted with chloroform-ethyl acetate (1:1, v/v) gave 4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2-piperidinomethylquinazoline (1.46 g, 65%). This compound was recrystallized from ethyl acetate - hexane. Colorless needles, mp. 130°-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650410
Source datasetuspto-grants-1997_07
ORD IDord-62b58b12b16246409ef872acfa573b56
Source noteuspto-grants-1997_07