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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452519Generated: October 31, 2026

Ethyl Acetate → HCID 57646682, compound

https://huagongshe.com/reaction/1452519

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

50 mg of 4-(2-chloropyridin-4-yl)-3-(4-fluorophenyl)-1-(2-cyanobenzy 1)-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 numberUS07473695B2
Source datasetuspto-grants-2009_01
ORD IDord-7aba503165ef4275803fd1085c4b2664
Source noteuspto-grants-2009_01