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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584673Generated: October 26, 2026

Potassium Carbonate → 6-Chloro-7-methylsulfanyl-2-(5-methyl-1,3,4-thiadiazol-2-ylsulfanyl)-3-trifluoromethylquinoxaline

https://huagongshe.com/reaction/584673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant6-chloro-7-methylsulfanyl-3-trifluoromethyl-1H-quinoxalin-2-oneHCID 22341150—
Reactant2,6-Dichloro-7-methylsulfanyl-3-trifluoromethylquinoxalineHCID 22341188—
ReactantHCID 178434161HCID 178434161—
SolventDimethylformamideHCID 6228—
Product6-Chloro-7-methylsulfanyl-2-(5-methyl-1,3,4-thiadiazol-2-ylsulfanyl)-3-trifluoromethylquinoxalineHCID 2234109650%

Reaction Conditions

Temperature50 °C

Reaction Steps

2,6-Dichloro-7-methylsulfanyl-3-trifluoromethylquinoxaline (116 mg, 0.37 mmol, prepared similarly as described above from 6-chloro-7-methylsulfanyl-3-trifluoromethyl-1H-quinoxaline-2-one, dimethylaminopyridine and POCl3) and 2-mercapto-5-methyl-1,3,4-thiadiazole (146 mg, 1.1 mmol) was dissolved in DMF (3.3 ml). Potassium carbonate (20 mg) was added and the reaction mixture was stirred at 50° C. for 2 hours. The cooled mixture was partitioned between diethyl ether and water. The organic layer separated, evaporated and the residue recrystallised from ethanol to afford 80 mg (50%) of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06927214B1
Source datasetuspto-grants-2005_08
ORD IDord-64b49224fe134921ba28c9bc0156e74e
Source noteuspto-grants-2005_08