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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918783Generated: October 31, 2026

Potassium Phosphate, Tribasic → HCID 72703861, compound

https://huagongshe.com/reaction/918783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
Reactant2-Bromo-6-(trifluoromethyl)imidazo[1,2-a]pyridineHCID 40148015—
Reactant2-(2-(Ethylthio)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 123787969—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 72703861HCID 7270386189.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 526 mg of 2-bromo-6-trifluoromethyl-imidazo[1,2-a]pyridine, 576 mg of 2-ethylsulfanylphenylboronic acid pinacol ester, 50 mg of tris(dibenzylideneacetone) dipalladium(0), 201 mg of tricyclohexylphosphine (18% toluene solution), 1.26 g of tripotassium phosphate, 4.5 ml of 1,4-dioxane and 1.5 ml of water was stirred at 100° C. for 2.5 hours. Ethyl acetate and water were poured to the cooled reaction mixture, and the mixture was filtered. The aqueous layer of the filtrate was extracted with ethyl acetate, then combined with the organic layer of the filtrate, and the mixture was washed with water and dried over anhydrous magnesium sulfate. The mixture was concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 570 mg of 2-(2-ethylsulfanylphenyl)-6-trifluoromethyl-imidazo[1,2-a]pyridine (hereinafter, referred to as Compound of Present Invention 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09271500B2
Source datasetuspto-grants-2016_03
ORD IDord-1c9300ef120e4780b33c33be3ac91b33
Source noteuspto-grants-2016_03