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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961370Generated: October 25, 2026

Diisopropylethylamine → 1-[4-(1-Benzhydryl-azetidin-3-yl)-piperazin-1-yl]-2,2,2-trifluoro-ethanone

https://huagongshe.com/reaction/1961370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(Diphenylmethyl)azetidin-3-yl methanesulfonateHCID 2758716—
ReactantTrifluoroacetylpiperazineHCID 7172020—
SolventAcetonitrileHCID 6342—
Product1-[4-(1-Benzhydryl-azetidin-3-yl)-piperazin-1-yl]-2,2,2-trifluoro-ethanoneHCID 59625975—

Reaction Steps

To a solution of 2,2,2-trifluoro-1-piperazin-1-yl-ethanone (6 g, 32.94 mmol) and 1-benzhydrylazetidin-3-yl methanesulfonate (12.5 g, 39.38 mmol) in CH3CN (60 mL) was added DIPEA (12 mL, 68.89 mmol) at room temperature. The resulting mixture was refluxed for 2 h. The solvent was removed by evaporation and the residue was partitioned between CH2Cl2 and aq NaHCO3. The organic layer was washed with aq NaHCO3 (2×) and then extracted with 1N HCl (2×). The aqueous layer was cooled and then the pH adjusted with 1N NaOH until basic (pH=10). The resulting mixture was extracted with CH2Cl2 (2×). The organic layer was dried over MgSO4 and concentrated. The title compound was purified by reverse phase chromatography. MS m/z (M+H+) 404.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415341B2
Source datasetuspto-grants-2013_04
ORD IDord-893899b95da4431baf8e5b74045dabaa
Source noteuspto-grants-2013_04