Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348874Generated: October 26, 2026

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

https://huagongshe.com/reaction/1348874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-ethyl-1,3,4-thiadiazoleHCID 26444—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
Reactant3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]anilineHCID 11739027—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductN-{3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-N'-(5-ethyl-1,3,4-thiadiazol-2-yl)ureaHCID 2311860732.7%

Reaction Steps

3-Chloro-4-[(6,7-dimethoxy-4-quinolyl)oxy]aniline (100 mg) was dissolved in chloroform (5 ml) and diisopropylethylamine (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 stirred at room temperature for 15 min. Next, 2-amino-5-ethyl-1,3,4-thiadiazole (41 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-f2c2b1c58a7f408f8c1e1a23336c258e
Source noteuspto-grants-2007_05