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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357886Generated: October 26, 2026

Cesium carbonate → HCID 11352447, compound

https://huagongshe.com/reaction/2357886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactant1-[2-(Trifluoromethyl)benzoyl]piperazineHCID 16733784—
ReactantTrifluoromethanesulfonic acid 6-(3-phenylpropylcarbamoyl)pyridin-3-yl esterHCID 86609725—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 11352447HCID 1135244713%

Reaction Steps

A 50-mL flask was charged with cesium carbonate (0.078 g, 0.238 mmol), palladium diacetate (0.0019 g, 0.0085 mmol) and BINAP (0.0079 g, 0.013 mmol) and flushed with argon for 30 minutes. A solution of trifluoromethanesulfonic acid 6-(3-phenylpropylcarbamoyl)pyridin-3-yl ester (0.066 g, 0.17 mmol) and piperazin-1-yl-(2-trifluoromethylphenyl)methanone (0.053 g, 0.20 mmol) in toluene (2 mL) was added via syringe. The reaction mixture was heated at 100 C for 26 h, cooled to room temperature, diluted with toluene (20 mL), filtered and concentrated in vacuo. The crude product was purified by column chromatography to afford the title compound as a white solid (0.011 g, 13% yield). 1H NMR (300 MHz, CDCl3) δ 8.15, 8.04, 7.85, 7.74, 7.50-7.65, 7.36, 7.30-7.10, 3.90-4.10, 3.55-3.30, 3.22, 2.72, 1.96. MS (ES+) m/z 497.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763618B2
Source datasetuspto-grants-2010_07
ORD IDord-40895d12926e4440adca47a06a901218
Source noteuspto-grants-2010_07