HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186303Generated: November 2, 2026
Dimethyl Sulfoxide → HCID 86657924, compound
https://huagongshe.com/reaction/1186303
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trifluoromethylsulfonamide | HCID 79001 | — |
| Reactant | HCID 86657923 | HCID 86657923 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86657924 | HCID 86657924 | 14% |
Reaction Steps
According to Example 132, by use of 2-chloro-3-[2,2,2-trifluoro-1-(pyridin-3-yl)ethoxy]-quinoxaline (Compound BJ) (70 mg, 0.21 mmol), dimethyl sulfoxide (2 mL), trifluoromethanesulfonamide (31 mg, 0.21 mmol) and potassium carbonate (28 mg, 0.21 mmol), the mixture was stirred and reacted at 150° C. for 1.5 hours. The reaction mixture was allowed to cool down to room temperature, a 1% aqueous acetic acid solution was added thereto, and extraction with ethyl acetate was performed. The organic layer was washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and then the solvent was evaporated off under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol=1/0 to 20/1). Further, slurry purification was performed using isopropyl ether, to give 1,1,1-trifluoro-N-{3-[2,2,2-trifluoro-1-(pyridin-3-yl)-ethoxy]quinoxalin-2-yl}methanesulfonamide (Compound 149) (13 mg, 14%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673908B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-b1ddb4e7b8434c85995a33bab106149f |
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| Source note | uspto-grants-2014_03 |
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