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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775297Generated: November 3, 2026

1,4-Dioxane → HCID 118205817, compound

https://huagongshe.com/reaction/1775297

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant7-bromo-2-(trifluoromethyl)imidazo[1,2-a]pyridineHCID 68294747—
Reactant2-(2-(Ethylthio)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 123787969—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 118205817HCID 11820581763.2%

Reaction Steps

A mixture of 0.53 g of 2-ethylsulfanylphenylboronic acid pinacol ester, 0.52 g of 7-bromo-2-trifluoromethylimidazo[1,2-a]pyridine, 0.02 g of tris(dibenzylideneacetone)dipalladium(0), 0.05 g of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylphenyl, 1.0 g of tripotassium phosphate and 6 ml of 1,4-dioxane was stirred under heat-reflux for 6 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 mixture was concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 0.40 g of 7-(2-ethylsulfanylphenyl)-2-trifluoromethylimidazo[1,2-a]pyridine (Compound of Present Invention 37).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260436B2
Source datasetuspto-grants-2016_02
ORD IDord-9bf6d0d9e9934190b1d8fd6caada0e4c
Source noteuspto-grants-2016_02