Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375891Generated: November 2, 2026

Water → N-(2-Chloro-4-{[6-methoxy-7-(2-pyridylmethoxy)-4-quinolyl]oxy}phenyl)-N'-propylurea

https://huagongshe.com/reaction/1375891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantPicolyl chloride hydrochlorideHCID 23392—
ReactantN-{2-chloro-4-[(7-hydroxy-6-methoxy-4-quinolyl)oxy)phenyl}-N'-propylureaHCID 135674220—
SolventDimethylformamideHCID 6228—
ProductN-(2-Chloro-4-{[6-methoxy-7-(2-pyridylmethoxy)-4-quinolyl]oxy}phenyl)-N'-propylureaHCID 2266703982%

Reaction Conditions

Temperature80 °C

Reaction Steps

A starting compound (N-{2-chloro-4-[(7-hydroxy-6-methoxy-4-quinolyl)oxy]phenyl}-N′-propylurea, 80 mg), potassium carbonate (138 mg), and 2-chloromethylpyridine hydrochloride (41 mg) were dissolved in N,N-dimethylformamide (1 ml), and the solution was stirred at 80° C. for 3 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. The solvent was removed by distillation under the reduced pressure. The residue was purified by HPLC to give 81 mg (yield 82%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169789B2
Source datasetuspto-grants-2007_01
ORD IDord-96786be1bd86482d9fafbdc853abd877
Source noteuspto-grants-2007_01