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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348864Generated: October 26, 2026

1,3,4-Thiadiazole, 2-amino-5-methyl- → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-3-methylphenyl}-N'-(5-methyl-1,3,4-thiadiazol-2-yl)urea

https://huagongshe.com/reaction/1348864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,4-Thiadiazole, 2-amino-5-methyl-HCID 66949—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
Reactant4-[(6,7-Dimethoxy-4-quinolyl)oxy]-3-methyl-anilineHCID 21891162—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductN-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-3-methylphenyl}-N'-(5-methyl-1,3,4-thiadiazol-2-yl)ureaHCID 2311861339.9%

Reaction Steps

4-[(6,7-Dimethoxy-4-quinolyl)oxy]-3-methylaniline (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-methyl-1,3,4-thiadiazole (49 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 58 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211587B2
Source datasetuspto-grants-2007_05
ORD IDord-f1130a4f061c4121b553f2b2fc523273
Source noteuspto-grants-2007_05