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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008412Generated: October 31, 2026

Triphosgene → N-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2-fluorophenyl}-N'-(2-propynyl)urea

https://huagongshe.com/reaction/1008412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
ReactantSodium BicarbonateHCID 516892—
ReactantProp-2-ynylamine hydrochlorideHCID 11205720—
Reactant4-((6,7-Dimethoxy-4-quinazolinyl)oxy]-2-fluoroanilineHCID 21890274—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductN-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2-fluorophenyl}-N'-(2-propynyl)ureaHCID 2266715333.5%

Reaction Steps

4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2-fluoro-aniline (50 mg) was dissolved in chloroform (3 ml) and triethylamine (0.3 ml), and a solution of triphosgene (47 mg) in chloroform was then added to the solution. The mixture was stirred at room temperature for 30 min. Next, propargylamine hydrochloride (29 mg) was added to the reaction solution, and the mixture was further stirred at room temperature overnight. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was washed with chloroform to give 21 mg (yield 33%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797823B1
Source datasetuspto-grants-2004_09
ORD IDord-425876e4ec444a22b26efd434973595c
Source noteuspto-grants-2004_09