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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713667Generated: November 3, 2026

Acetone → 3-ethylsulfonyl-N-methyl-N-[4-(2,2,2-trifluoro-1,1-dimethoxyethyl)phenyl]picolinamide

https://huagongshe.com/reaction/713667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-ethylsulfonyl-N-[4-(2,2,2-trifluoro-1,1-dimethoxyethyl)phenyl]picolinamideHCID 118113335—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-ethylsulfonyl-N-methyl-N-[4-(2,2,2-trifluoro-1,1-dimethoxyethyl)phenyl]picolinamideHCID 118113400104.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

1.0 g of methyl iodide was added to a mixture of 0.12 g of 3-ethylsulfonyl-N-[4-(2,2,2-trifluoro-1,1-dimethoxyethyl)phenyl]picolinamide (Compound of Present Invention 42), 0.15 g of potassium carbonate, 2 mL of acetone and 2 mL of DMF, and the mixture was stirred at 80° C. for 3 hours. Water was added 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 0.13 g of 3-ethylsulfonyl-N-methyl-N-[4-(2,2,2-trifluoro-1,1-dimethoxyethyl)phenyl]picolinamide (hereinafter, referred to as Compound of Present Invention 43).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09185910B2
Source datasetuspto-grants-2015_11
ORD IDord-5342da91b2d44a96aff5b2008d6df9e9
Source noteuspto-grants-2015_11