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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 1-(Chloromethyl)-2,4-dimethoxybenzene | HCID 18505261 | — |
| 반응물 | trans 5-(3-Chlorophenyl)-6-(5-chloropyridin-2-yl)piperidin-2-one | HCID 86660724 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (5R,6S)-5-(3-chlorophenyl)-6-(5-chloropyridin-2-yl)-1-(2,4-dimethoxybenzyl)piperidin-2-one | HCID 58573798 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09296736B2 |
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| 출처 데이터셋 | uspto-grants-2016_03 |
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| ORD ID | ord-36341ded1aca46c588092de82d4595c3 |
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| 출처 메모 | uspto-grants-2016_03 |
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