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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386322Generated: October 31, 2026

Thionyl Chloride → 4-Chloro-7-(3-(morpholin-4-yl)propoxy)quinazoline

https://huagongshe.com/reaction/1386322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant7-(3-Morpholinopropoxy)-3,4-dihydroquinazolin-4-oneHCID 135798752—
SolventDimethylformamideHCID 6228—
Product4-Chloro-7-(3-(morpholin-4-yl)propoxy)quinazolineHCID 2169929780%

Reaction Steps

A mixture of 7-(3-morpholinopropoxy)-3,4-dihydroquinazolin-4-one (500 mg, 1.7 mmol), thionyl chloride (10 ml) and DMF (0.1 ml) was heated at reflux for 2 hours. The volatiles were removed by evaporation and the residue azeotroped with toluene. The crude product was partitioned between methylene chloride (50 ml) and saturated aqueous sodium hydrogen carbonate solution (50 ml) and the mixture stirred for 10 minutes. The organic phase was separated and the aqueous phase extracted with methylene chloride. The combined extracts were dried (MgSO4) and the solvent removed by evaporation to give 4-chloro-7-(3-morpholinopropoxy)quinazoline (425 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265411B1
Source datasetuspto-grants-2001_07
ORD IDord-ba680be453f24c109c4a381d8fd980c5
Source noteuspto-grants-2001_07