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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1961370Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1961370

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1-(Diphenylmethyl)azetidin-3-yl methanesulfonateHCID 2758716—
EduktTrifluoroacetylpiperazineHCID 7172020—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-[4-(1-Benzhydryl-azetidin-3-yl)-piperazin-1-yl]-2,2,2-trifluoro-ethanoneHCID 59625975—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08415341B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-893899b95da4431baf8e5b74045dabaa
Quellennotizuspto-grants-2013_04