HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713664Generated: October 28, 2026
Acetone → 3-ethylsulfonyl-N-methyl-N-(4-trifluoromethoxyphenyl)picolinamide
https://huagongshe.com/reaction/713664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-ethylsulfonyl-N-(4-trifluoromethoxyphenyl)picolinamide | HCID 118113485 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-ethylsulfonyl-N-methyl-N-(4-trifluoromethoxyphenyl)picolinamide | HCID 118205930 | 91.6% |
Reaction Steps
0.50 g of methyl iodide was added to a mixture of 0.20 g of 3-ethylsulfonyl-N-(4-trifluoromethoxyphenyl)picolinamide (Compound of Present Invention 21), 0.12 g of potassium carbonate and 3 mL of acetone, and the mixture was stirred at room temperature for 1 hour. 1 mL of DMF was added to the reaction mixture, and the mixture was stirred at 60° C. for 2 hours. Water was poured to the reaction mixture cooled to room temperature, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 0.19 g of 3-ethylsulfonyl-N-methyl-N-(4-trifluoromethoxyphenyl)picolinamide (hereinafter, referred to as Compound of Present Invention 39).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09185910B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-78b3446fff6849148c8aab41da674e94 |
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| Source note | uspto-grants-2015_11 |
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