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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008466Generated: October 31, 2026

Water → N-{2-Chloro-4-[(7-{2-[(2-hydroxyethyl)-(methyl)amino]ethoxy}-6-methoxy-4-quinolyl)oxy]phenyl}-N'-(2,4-difluorophenyl)urea

https://huagongshe.com/reaction/1008466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-(Methylamino)ethanolHCID 8016—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22667123HCID 22667123—
SolventDimethylformamideHCID 6228—
ProductN-{2-Chloro-4-[(7-{2-[(2-hydroxyethyl)-(methyl)amino]ethoxy}-6-methoxy-4-quinolyl)oxy]phenyl}-N'-(2,4-difluorophenyl)ureaHCID 2266723797%

Reaction Steps

A starting compound (N-(4-{[7-(2-bromoethoxy)-6-methoxy-4-quinolyl]oxy}-2-chlorophenyl)-N′-(2,4-difluorophenyl)urea, 50 mg), potassium carbonate (138 mg), and 2-(methylamino)ethanol (0.040 ml) were dissolved in N,N-dimethylformamide (1 ml), and the solution was stirred at room temperature for 18 hr. Water was added to the reaction mixture, and the mixture was extracted with chloroform-propanol (3/1). The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed by distillation under the reduced pressure. The residue was washed with ether to give 48 mg (yield 97%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797823B1
Source datasetuspto-grants-2004_09
ORD IDord-12cc08abdf494186937675bfd4391ea3
Source noteuspto-grants-2004_09