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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1961370생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1961370

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1-(Diphenylmethyl)azetidin-3-yl methanesulfonateHCID 2758716—
반응물TrifluoroacetylpiperazineHCID 7172020—
용매AcetonitrileHCID 6342—
생성물1-[4-(1-Benzhydryl-azetidin-3-yl)-piperazin-1-yl]-2,2,2-trifluoro-ethanoneHCID 59625975—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08415341B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-893899b95da4431baf8e5b74045dabaa
출처 메모uspto-grants-2013_04