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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-ethylsulfonyl-N-(4-trifluoromethoxyphenyl)picolinamideHCID 118113485—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-ethylsulfonyl-N-methyl-N-(4-trifluoromethoxyphenyl)picolinamideHCID 11820593091.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09185910B2
Source datasetuspto-grants-2015_11
ORD IDord-78b3446fff6849148c8aab41da674e94
Source noteuspto-grants-2015_11