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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634755Generated: November 1, 2026

Toluene → 4-Chloro-6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazoline

https://huagongshe.com/reaction/634755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Reactant6-methoxy-7-(3-morpholin-4-ylpropoxy)-1H-quinazolin-4-oneHCID 178486772—
Product4-Chloro-6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolineHCID 1182394166%

Reaction Steps

A solution of 4-hydroxy-6-methoxy-7-(3-morpholinopropoxy)quinazoline (2.87 g, 9 mmol) and DMF (1 ml) in thionyl chloride (35 ml) was refluxed for 45 minutes. After addition of toluene, the volatiles were removed by evaporation. The residue was partitioned between ethyl acetate and water and the aqueous layer was adjusted to pH8 with 2M aqueous sodium hydroxide. The organic layer was washed with water and brine, dried (MgSO4) and the volatiles were removed by evaporation. The solid residue was purified by column chromatography eluting with a mixture of methylene chloride, acetonitrile and methanol (50/47.5/2.5) to give 4-chloro-6-methoxy-7-(3-morpholinopropoxy)quinazoline (2 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184225B2
Source datasetuspto-grants-2001_02
ORD IDord-388f0d8624944a8a89f1c801f19366a8
Source noteuspto-grants-2001_02