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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184733Generated: November 1, 2026

Ethyl Acetate → HCID 57389225, compound

https://huagongshe.com/reaction/1184733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
Reactant(1,1'-Binaphthalen)-2-yldi-tert-butylphosphineHCID 2734941—
ReactantHCID 67973476HCID 67973476—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 57389225HCID 57389225—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 4-{2-[5-chloro-2-(4-methanesulfonyl-phenyl)-pyrimidin-4-yl]-1-hydroxy-ethyl}-piperidine-1-carboxylic acid tert-butyl ester (50 mg), palladium acetate (3 mg), racemic 2-(di-tert-butylphosphino)-1,1′-binapthyl (6 mg), and cesium carbonate (50 mg) in toluene (1 mL) is heated in an oil bath at 70° C. under an argon atmosphere for 6 h. After cooling to room temperature ethyl acetate is added and the organic phase is separated, washed with water and brine, dried over MgSO4, and concentrated in vacuo. The residue is chromatographed on silica gel [dichloromethane/(dichloromethane/methanol/NH4OH 24:24:1) 96:4→90:10]. The crude product is triturated with diethyl ether, filtered off, and dried to give the title compound. LC (method 7): tR=1.44 min; Mass spectrum (ESI+): m/z=460 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669271B2
Source datasetuspto-grants-2014_03
ORD IDord-c05aaccbb9aa478ba44e1cc039664951
Source noteuspto-grants-2014_03