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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

반응식

참여 물질

역할이름HCID투입량
반응물1-Methyl-4-piperidoneHCID 74049—
반응물2-Bromo-5-(2-methyl-1,3-dioxolan-2-yl)pyridineHCID 85775099—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-Methyl-4-(5-(2-methyl-1,3-dioxolan-2-yl)pyridin-2-yl)piperidin-4-olHCID 5746584685%

반응 조건

온도-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08962642B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-3a09eb135c464493bad342fe7685d6d6
출처 메모uspto-grants-2015_02