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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008415Generated: October 25, 2026

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

https://huagongshe.com/reaction/1008415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBenzene, 1-isocyanato-2-methoxy-HCID 69695—
Reactant4-((6,7-Dimethoxy-4-quinazolinyl)oxy]-2-fluoroanilineHCID 21890274—
SolventChloroformHCID 6212—
ProductN-{4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2-fluorophenyl}-N'-(2-methoxyphenyl)ureaHCID 2266717530%

Reaction Conditions

Temperature60 °C

Reaction Steps

4-[(6,7-Dimethoxy-4-quinazolinyl)oxy]-2-fluoro-aniline (50 mg) was dissolved in chloroform (3 ml), and 2-methoxyphenyl isocyanate (32 μl) was then added to the solution. The mixture was stirred at 60° C. overnight. Methanol was added to the reaction solution, and the mixture was purified by HPLC by development with chloroform/methanol to give 22 mg (yield 30%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797823B1
Source datasetuspto-grants-2004_09
ORD IDord-4a64358cf0bd4ba69a26d78485ca4aa3
Source noteuspto-grants-2004_09