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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634708Generated: October 31, 2026

Thionyl Chloride → 4-Chloro-6-methoxy-7-(2-(4-methylpiperazin-1-yl)ethoxy)quinazoline

https://huagongshe.com/reaction/634708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 135509428HCID 135509428—
CatalystDimethylformamideHCID 6228—
Product4-Chloro-6-methoxy-7-(2-(4-methylpiperazin-1-yl)ethoxy)quinazolineHCID 1175949923%

Reaction Steps

A mixture of 6-methoxy-7-(2-(4-methylpiperazin-1-yl)ethoxy)-3,4-dihydroquinazolin-4-one (500 mg, 1.57 mmol), thionyl chloride (20 ml) and DMF (3 drops) was heated at reflux for 3 hours and allowed to cool. The excess thionyl chloride was removed by evaporation, and the residue was azeotroped with toluene. The residue was treated with aqueous sodium hydrogen carbonate and the product was extracted with methylene chloride. The combined extracts were washed with brine, passed through phase separating paper and the solvent removed by evaporation to give 4-chloro-6-methoxy-7-(2-(4-methylpiperazin-1-yl)ethoxy)quinazoline (120 mg, 23%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184225B2
Source datasetuspto-grants-2001_02
ORD IDord-bd786e9e21684ada878577c23a704115
Source noteuspto-grants-2001_02