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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838593Generated: October 30, 2026

Dimethylcarbamoyl Chloride → 4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-(N',N',N-trimethylureido)ethoxy)quinazoline hydrochloride

https://huagongshe.com/reaction/1838593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
ReactantTriethylamineHCID 8471—
Reactant4-(4-Chloro-2-fluoroanilino)-6-methoxy-7-(2-methylaminoethoxy)quinazolineHCID 22478192—
SolventDichloromethaneHCID 6344—
Product4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-(N',N',N-trimethylureido)ethoxy)quinazoline hydrochlorideHCID 6980843641.3%

Reaction Steps

Dimethylcarbamyl chloride (38 μl, 0.42 mmol) was added to a solution of 4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-methylaminoethoxy)quinazoline (150 mg, 0.4 mmol), (prepared as described for the starting material in Example 60), and triethylamine (61 μl, 0.44 mmol) in methylene chloride (4 ml). The mixture was stirred for 2.5 hours at ambient temperature, the resulting precipitate was collected by filtration and washed with ether. The solid was purified by column chromatography, eluting with methylene chloride/methanol (92/8). The purified product was dissolved in methylene chloride/methanol (1/1), 2.9M ethereal hydrogen chloride (1 ml) was added and the volatiles were removed by evaporation. The residue was triturated with ether and the solid product collected by filtration, washed with ether and dried under vacuum to give 4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-(N′, N′, N-trimethylureido)ethoxy)quinazoline hydrochloride (80 mg, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673803B2
Source datasetuspto-grants-2004_01
ORD IDord-518a264e1c944052a47cd38cd0f65b0a
Source noteuspto-grants-2004_01