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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775287Generated: November 1, 2026

1,4-Dioxane → 6-(2-Ethylsulfanylphenyl)-5-methyl-2-trifluoromethylimidazo [1,2-a]pyridine

https://huagongshe.com/reaction/1775287

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant6-Bromo-5-methyl-2-trifluoromethylimidazo[1,2-a]pyridineHCID 115403721—
Reactant2-(2-(Ethylthio)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 123787969—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product6-(2-Ethylsulfanylphenyl)-5-methyl-2-trifluoromethylimidazo [1,2-a]pyridineHCID 11820583224.2%

Reaction Steps

A mixture of 0.52 g of 2-ethylsulfanylphenylboronic acid pinacol ester, 0.56 g of 6-bromo-5-methyl-2-trifluoromethylimidazo[1,2-a]pyridine, 0.02 g of tris(dibenzylideneacetone)dipalladium(0), 0.05 g of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylphenyl, 0.84 g of tripotassium phosphate and 6 ml of 1,4-dioxane was stirred under heat-reflux for 3 hours. 0.1 ml of water was added to the cooled reaction mixture, and the mixture was stirred under heat-reflux for 5 hours. Ethyl acetate and water were added to the cooled reaction mixture, and the mixture was filtered. The filtrate was extracted with ethyl acetate and then dried over anhydrous sodium sulfate. The dried matter was concentrated under reduced pressure, and then the resulting residue was applied to a silica gel column chromatography to obtain 0.16 g of 6-(2-ethylsulfanylphenyl)-5-methyl-2-trifluoromethylimidazo [1,2-a]pyridine (Compound of Present Invention 28).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260436B2
Source datasetuspto-grants-2016_02
ORD IDord-ed8d57c3854e418aa418274ff0307010
Source noteuspto-grants-2016_02