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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261021Generated: October 30, 2026

Ethyl Acetate → HCID 57646682, compound

https://huagongshe.com/reaction/2261021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1-Phenethylamine, (-)-HCID 75818—
ReactantHCID 23020386HCID 23020386—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 57646682HCID 57646682—

Reaction Conditions

Temperature70 °C

Reaction Steps

4-(2-Chloropyridin-4-yl)-3-(4-fluorophenyl)-1-(2-cyanobenzyl)-4-imidazolin-2-one (a compound of Reference Example 1 (6)), 79 μl of (S)-(−)-α-methylbenzylamine, 5.5 mg of palladium acetate, 15 mg of 2,2′-bis(diphenylphsophino)-1,1′-binaphthyl and 17 mg of sodium t-butoxide were suspended in 1 ml of toluene, and the mixture was stirred at 70° C. for 18 hours, under nitrogen flow. The reaction mixture was diluted by ethyl acetate, and insoluble matter was removed by filtration through Celite. To the filtrate was added 6N hydrochloric acid, and after separation, an aqueous layer was made alkaline with aqueous sodium bicarbonate solution. The mixture was extracted with chloroform, washed with saturated brine, and dried over anhydrous magnesium sulfate. After concentration under reduced pressure, the residue was purified by silica gel column chromatography (hexane ethyl acetate=1:2), to give 38 mg of the title compound as colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846933B2
Source datasetuspto-grants-2010_12
ORD IDord-943997ed9c0d4b0891a669fa32137a05
Source noteuspto-grants-2010_12