Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1853481생성일: 2026년 10월 27일
1-Methyl-4-piperidone → 1-Methyl-4-(5-(2-methyl-1,3-dioxolan-2-yl)pyridin-2-yl)piperidin-4-ol
https://huagongshe.com/reaction/1853481
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1-Methyl-4-piperidone | HCID 74049 | — |
| 반응물 | 2-Bromo-5-(2-methyl-1,3-dioxolan-2-yl)pyridine | HCID 85775099 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-Methyl-4-(5-(2-methyl-1,3-dioxolan-2-yl)pyridin-2-yl)piperidin-4-ol | HCID 57465846 | 85% |
반응 단계
2-bromo-5-(2-methyl-1,3-dioxolan-2-yl)pyridine (500 mg, 2.048 mmol) (described in the literature: Bioorg. Med. Chem., 2005, 13, 6763) was dissolved in anhydrous tetrahydrofuran (10 mL) and cooled to −78° C. under nitrogen. n-BuLi (901.2 μL of 2.5 M, 2.253 mmol) was added dropwise and the reaction mixture was stirred at −78° C. for 30 minutes. 1-Methyl-4-piperidone (602.6 mg, 655.0 μL, 5.325 mmol) was added and the reaction was allowed to stir at −78° C. for 20 minutes then warmed slowly to ambient temperature. The reaction mixture was stirred at room temperature for 18 hours and concentrated in vacuo. The residue was purified on silica gel by flash column chromatography to afford the title compound as a sticky orange solid (483.4 mg, 85% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08962642B2 |
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| 출처 데이터셋 | uspto-grants-2015_02 |
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| ORD ID | ord-3a09eb135c464493bad342fe7685d6d6 |
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| 출처 메모 | uspto-grants-2015_02 |
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