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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375815Generated: October 27, 2026

Benzene, 1-isocyanato-2-methoxy- → N-(4-{[7-(Benzyloxy)-6-methoxy-4-quinolyl]oxy}-2,3-dimethylphenyl)-N'-(2-methoxyphenyl)-urea

https://huagongshe.com/reaction/1375815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-isocyanato-2-methoxy-HCID 69695—
ReactantSodium BicarbonateHCID 516892—
Reactant4-{[7-(Benzyloxy)-6-methoxy-4-quinolyl]oxy}-2,3-dimethylanilineHCID 22667150—
SolventDimethylformamideHCID 6228—
ProductN-(4-{[7-(Benzyloxy)-6-methoxy-4-quinolyl]oxy}-2,3-dimethylphenyl)-N'-(2-methoxyphenyl)-ureaHCID 2266707247.4%

Reaction Steps

4-{[7-(Benzyloxy)-6-methoxy-4-quinolyl]oxy}-2,3-dimethylaniline (260 mg) was dissolved in N,N-dimethylformamide (5 ml), and 2-methoxyphenyl isocyanate (116 mg) was then added to the solution. The mixture was allowed to react 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 magnesium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by thin-layer chromatography on silica gel by development with chloroform/acetone (2/1) to give 169 mg (yield 47%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169789B2
Source datasetuspto-grants-2007_01
ORD IDord-ab240bab70fa48ccaa7831c0b5380a87
Source noteuspto-grants-2007_01