Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348880Generated: October 30, 2026

Triethylamine → N-{2-Chloro-4-[(6,7-dimethoxy-4-quinolyl)-oxy]phenyl}-N'-[5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl]urea

https://huagongshe.com/reaction/1348880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,3,4-Thiadiazol-2-amine, 5-(trifluoromethyl)-HCID 82634—
ReactantTriphosgeneHCID 94429—
Reactant4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-chloroanilineHCID 11221223—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductN-{2-Chloro-4-[(6,7-dimethoxy-4-quinolyl)-oxy]phenyl}-N'-[5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl]ureaHCID 2311860630.2%

Reaction Steps

2-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]aniline (100 mg) was dissolved in chloroform (5 ml) and triethylamine (0.5 ml) to prepare a solution. A solution of triphosgene (100 mg) in chloroform was then added to the solution, and the mixture was then stirred at room temperature for 15 min. Next, 2-amino-5-trifluoromethyl-1,3,4-thiadiazole (65 mg) was added thereto, and the mixture was further stirred at room temperature overnight. Distilled water was added to the reaction solution, and the mixture was subjected to separatory extraction with chloroform. The organic layer was washed with saturated brine and was dried over sodium sulfate. The organic layer was concentrated under the reduced pressure, and the residue was purified by HPLC using chloroform/acetone for development to give 48 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211587B2
Source datasetuspto-grants-2007_05
ORD IDord-40a1b90772d048b28272a79914386906
Source noteuspto-grants-2007_05