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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604681Generated: October 25, 2026

Sodium Carbonate → (4S,5R)-5-[3,5-Bis(trifluoromethyl)phenyl]-3-{[6-chloro-3-(2-fluoro-5-nitrophenyl)pyridin-2-yl]methyl}-4-methyl-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/604681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(2-Fluoro-5-nitrophenyl)boronic acidHCID 2763280—
Reactant(4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-3-[(3-bromo-6-chloropyridin-2-yl)methyl]-4-methyl-1,3-oxazolidin-2-oneHCID 57576268—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthanol toluene waterHCID 86587398—
Product(4S,5R)-5-[3,5-Bis(trifluoromethyl)phenyl]-3-{[6-chloro-3-(2-fluoro-5-nitrophenyl)pyridin-2-yl]methyl}-4-methyl-1,3-oxazolidin-2-oneHCID 86627635—

Reaction Steps

A mixture of INTERMEDIATE 9 (1.0 g, 1.93 mmol), 2-fluoro-5-nitro phenyl boronic acid (0.51 g, 2.74 mmol), tetrakis(triphenylphosphine) palladium (223 mg, 10% mol) and Na2CO3 (410 mg, 3.86 mmol) in 14 mL of water/EtOH/toluene (1:2:4) was heated at reflux for 2 h. The solvents were removed. Water (20 mL) was added. The organic was extracted with CH2Cl2 (3×10 mL). The combined CH2Cl2 layers were washed with brine, and dried (Na2SO4). The title compound was obtained after flash chromatography using CH2Cl2/hexane (8:2) as the eluant. LCMS M+H 578.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910592B2
Source datasetuspto-grants-2011_03
ORD IDord-7fa6edd879aa48239f9a8a9016bef31d
Source noteuspto-grants-2011_03