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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737641Generated: October 31, 2026

Toluene → 4-Chloro-6-methoxy-7-(2-(1,2,4-triazol-1-yl)ethoxy)quinazoline

https://huagongshe.com/reaction/1737641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Reactant6-Methoxy-7-(2-(1,2,4-triazol-1-yl)ethoxy)-3,4-dihydroquinazolin-4-oneHCID 135671175—
Product4-Chloro-6-methoxy-7-(2-(1,2,4-triazol-1-yl)ethoxy)quinazolineHCID 2262489665%

Reaction Steps

A solution of 6-methoxy-7-(2-(1,2,4-triazol-1-yl)ethoxy)-3,4-dihydroquinazolin-4-one (1.11 g, 3.86 mmol) and DMF (0.6 ml) in thionyl chloride (15 ml) was heated at reflux for 1 hour. The mixture was allowed to cool, toluene was added and the volatiles were removed by evaporation. The residue was partitioned between methylene chloride and water and the aqueous layer was adjusted to pH8.5 with saturated aqueous sodium hydrogen carbonate solution. The organic layer was separated, washed with brine, dried (MgSO4), and the solvent removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/methanol (95/5). The purified solid was triturated with ether, collected by filtration, washed with water and then ether, and dried under vacuum to give 4-chloro-6-methoxy-7-(2-(1,2,4-triazol-1-yl)ethoxy)quinazoline (756 mg, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962458
Source datasetuspto-grants-1999_10
ORD IDord-10cb9ea8a16945909ec97e5c5311802c
Source noteuspto-grants-1999_10