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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733415Generated: October 26, 2026

Water → 2,2,2-Trifluoro-1-[3-(5-methoxy-3-pyridin-3-yl-9H-xanthen-9-yl)-8-aza-bicyclo[3.2.1]oct-8-yl]-ethanone

https://huagongshe.com/reaction/733415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant3-Pyridinylboronic acidHCID 2734378—
Reactant1-[3-(3-Bromo-5-methoxy-9H-xanthen-9-yl)-8-aza-bicyclo[3.2.1]oct-8-yl]-2,2,2-trifluoro-ethanoneHCID 57839243—
Catalystdi-tert-butylphosphine palladium (II) dichlorideHCID 86605581—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product2,2,2-Trifluoro-1-[3-(5-methoxy-3-pyridin-3-yl-9H-xanthen-9-yl)-8-aza-bicyclo[3.2.1]oct-8-yl]-ethanoneHCID 5783922793%

Reaction Steps

To a solution of 1-[3-(3-bromo-5-methoxy-9H-xanthen-9-yl)-8-aza-bicyclo[3.2.1]oct-8-yl]-2,2,2-trifluoro-ethanone, 5k (0.505 g, 1.02 mmol) in dioxane (15 mL) were added 3-pyridylboronic acid (0.188 g, 1.53 mmol), di-tert-butylphosphine palladium (II) dichloride (35 mg), and a 2 M sodium carbonate solution (1.3 mL, 2.54 mmol), and the mixture was heated at 75° C. for 2 h under an argon atmosphere. The mixture was allowed to cool to rt and water and ethyl acetate were added. The organic phase was washed with brine, dried over MgSO4, filtered and concentrated. The residue was purified by flash column chromatography (eluent gradient: 50% to 95% EtOAc in heptane) to yield 0.47 g (93%) of title compound 2,2,2-trifluoro-1-[3-(5-methoxy-3-pyridin-3-yl-9H-xanthen-9-yl)-8-aza-bicyclo[3.2.1]oct-8-yl]-ethanone, 6k. MS m/z (MH+) 495.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589104B2
Source datasetuspto-grants-2009_09
ORD IDord-eae0f85871e74f45bc94dec936af6a4e
Source noteuspto-grants-2009_09