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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 932056생성일: 2026년 10월 25일

Acetic Acid → (5R,6S)-5-(3-chlorophenyl)-6-(5-chloropyridin-2-yl)-1-(2,4-dimethoxybenzyl)piperidin-2-one

https://huagongshe.com/reaction/932056

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium hydrideHCID 24758—
반응물Sodium BicarbonateHCID 516892—
반응물1-(Chloromethyl)-2,4-dimethoxybenzeneHCID 18505261—
반응물trans 5-(3-Chlorophenyl)-6-(5-chloropyridin-2-yl)piperidin-2-oneHCID 86660724—
용매DimethylformamideHCID 6228—
생성물(5R,6S)-5-(3-chlorophenyl)-6-(5-chloropyridin-2-yl)-1-(2,4-dimethoxybenzyl)piperidin-2-oneHCID 58573798—

반응 조건

온도0 °C

반응 단계

To a solution of 6.72 g (20.92 mmol) of (5R,6S)-5-(3-chlorophenyl)-6-(5-chloropyridin-2-yl)piperidin-2-one (Example 121, Step F) in DMF (˜0.5M) at 0° C. was slowly added a dispersion of 60% sodium hydride in mineral oil (2.51 g, 62.8 mmol). The reaction was stirred 0° C. for 30 min, followed by addition of 1-(chloromethyl)-2,4-dimethoxybenzene (7.81 g, 41.8 mmol). Upon completion, the reaction was quenched at 0° C. with a small excess of acetic acid (4.79 mL, 84 mmol). It was neutralized with sat. aq. NaHCO3 solution and extracted with ethyl acetate. The organic layer was dried over Na2SO4, filtered and the filtrate as concentrated under reduced pressure to yield a reddish oil. Purification by flash chromatography on silica gel (eluent: 0 to 30% ethyl acetate/DCM, gradient elution) provided the title compound as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09296736B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-36341ded1aca46c588092de82d4595c3
출처 메모uspto-grants-2016_03