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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-chloro-7-methylsulfanyl-3-trifluoromethyl-1H-quinoxalin-2-one | HCID 22341150 | — |
| Reactant | 2,6-Dichloro-7-methylsulfanyl-3-trifluoromethylquinoxaline | HCID 22341188 | — |
| Reactant | HCID 178434161 | HCID 178434161 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Chloro-7-methylsulfanyl-2-(5-methyl-1,3,4-thiadiazol-2-ylsulfanyl)-3-trifluoromethylquinoxaline | HCID 22341096 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06927214B1 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-64b49224fe134921ba28c9bc0156e74e |
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| Source note | uspto-grants-2005_08 |
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