Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375169Generated: November 2, 2026

Water → HCID 21079510, compound

https://huagongshe.com/reaction/1375169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantTivozanibHCID 9911830—
SolventAcetonitrileHCID 6342—
SolventDimethylacetamideHCID 31374—
ProductHCID 21079510HCID 2107951084%

Reaction Steps

N-{2-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N′-(5-methyl-3-isoxazolyl)urea (2.0 g) produced in Production Example was added to acetonitrile (27 mL), a solution of p-toluenesulfonic acid monohydrate (2.5 g) in acetonitrile (27 mL) was added dropwise thereto, and the mixture was stirred at room temperature for 3 hr. The resultant precipitate was collected by filtration and the filtered product was then dried under the reduced pressure. The powder thus obtained was stirred in N,N-dimethylacetamide (10 mL) at 100° C. for complete dissolution. The solution was then cooled to room temperature, and water (10 mL) was added dropwise thereto. The mixture was cooled to 5° C. and was stirred at that temperature overnight. The resultant precipitate was filtered, and the filtered product was then dried under the reduced pressure to give a form II crystal of N-{2-chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N′-(5-methyl-3-isoxazolyl)urea p-toluenesulfonate (2.3 g, yield 84.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166722B2
Source datasetuspto-grants-2007_01
ORD IDord-8b6f8ff6236b47458fe3e3b3ecd6e21f
Source noteuspto-grants-2007_01