Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375844Generated: October 31, 2026

Methanol → N-(sec-Butyl)-N'-{4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-2-fluorophenyl}urea

https://huagongshe.com/reaction/1375844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSec-ButylamineHCID 24874—
ReactantTriphosgeneHCID 94429—
Reactant4-((6,7-Dimethoxy-4-quinazolinyl)oxy]-2-fluoroanilineHCID 21890274—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
ProductN-(sec-Butyl)-N'-{4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-2-fluorophenyl}ureaHCID 2266718818%

Reaction Steps

4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2-fluoroaniline (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, sec-butylamine (25 μl) was added to the reaction solution, and the mixture was further stirred at room temperature overnight. Methanol was added to the reaction solution, and the mixture was purified by HPLC by development with chloroform/methanol to give 12 mg (yield 18%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169789B2
Source datasetuspto-grants-2007_01
ORD IDord-ae8441c09bea4ba1a04ebef84918e24e
Source noteuspto-grants-2007_01