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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823101Generated: November 1, 2026

Sodium Carbonate → HCID 24822473, compound

https://huagongshe.com/reaction/1823101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-Fluoro-4-(methoxycarbonyl)benzeneboronic acidHCID 2782818—
ReactantHCID 24822466HCID 24822466—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
ProductHCID 24822473HCID 2482247376.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-[2-[(tert-butoxycarbonyl)[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino]ethyl]phenyl trifluoromethanesulfonate (300 mg) in 1,2-dimethoxyethane (5 ml) was added [3-fluoro-4-(methoxycarbonyl)phenyl]boronic acid (125 mg), tetrakis(triphenylphosphine)palladium (53 mg) and aqueous solution of sodium carbonate (2M, 0.6 ml), and the mixture was stirred at 80° C. for 2 hours under nitrogen. The mixture was diluted with ethyl acetate and water. The organic layer was separated, washed with brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=3/1) to give methyl 4′-[2-[(tert-butoxycarbonyl)[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino]ethyl]-3-fluoro-1,1′-biphenyl-4-carboxylate (230 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037938B2
Source datasetuspto-grants-2006_05
ORD IDord-649472b2c75641799ca217da63d40377
Source noteuspto-grants-2006_05