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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994625Generated: October 30, 2026

Nitrogen → HCID 11606755, compound

https://huagongshe.com/reaction/1994625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPotassium HydroxideHCID 14797—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactant(4-Fluoro-5-isopropyl-2-methoxyphenyl)boronic acidHCID 53363739—
Reactant(4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-3-(2-chloro-4-fluorobenzyl)-4-methyl-1,3-oxazolidin-2-oneHCID 59135207—
Catalystpalladium(II) acetateHCID 167845—
SolventHexaneHCID 8058—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 11606755HCID 11606755—

Reaction Steps

To a solution of (4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-3-(2-chloro-4-fluorobenzyl)-4-methyl-1,3-oxazolidin-2-one (100 mg, 0.22 mmol) in 1,4-dioxane (1 mL) was added (4-fluoro-5-isopropyl-2-methoxyphenyl)boronic acid (55.8 mg, 0.26 mmol), palladium(II) acetate (10 mg, 20 mol %), potassium hydroxide aqueous solution (147 μL, 3M, 2 eq.) and tri-tert-butylphosphine (13.4 mg, 0.066 mmol, 30 mol % as a 10% w/w hexane solution). The resulting reaction mixture was N2 purged and sealed in a microwave vessel. The vessel was subject to microwave irradiation at 140° C. for 40 min. LC-MS indicated the formation of desired product. It was quenched with water (50 mL). Volatiles were evaporated. The resulting mixture was extracted with EtOAc. The combined extracts were dried over Na2SO4, filtered and concentrated in vacuo to an oil. The titled compound was obtained after two purifications with silica gel and one reversed phase prep-HPLC. LC-MS:588.25 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652049B2
Source datasetuspto-grants-2010_01
ORD IDord-bdd5f94926e64a1cac68711af18c9d3c
Source noteuspto-grants-2010_01