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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 408294생성일: 2026년 10월 24일

(3R)-3-Aminopiperidine, 3-BOC protected → (R)-tert-butyl 1-(5-bromo-3-(3-fluoro-4-methoxybenzamido)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-ylcarbamate

https://huagongshe.com/ko/reaction/408294

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참여 물질

역할이름HCID투입량
반응물(3R)-3-Aminopiperidine, 3-BOC protectedHCID 1514172—
반응물N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-3-fluoro-4-methoxybenzamideHCID 60205472—
용매1-ButanolHCID 263—
생성물(R)-tert-butyl 1-(5-bromo-3-(3-fluoro-4-methoxybenzamido)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-ylcarbamateHCID 6704550627.2%

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온도155 °C

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A mixture of N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-3-fluoro-4-methoxybenzamide (300 mg, 0.785 mmol) and (R)-tert-butyl piperidin-3-ylcarbamate (472 mg, 2.36 mmol) in n-BuOH (3 mL) was stirred at 155° C. for 16 hours in a sealed tube. The reaction was then cooled to room temperature and concentrated in vacuo. The resulting residue was purified by reverse phase HPLC (Gilson) to provide (R)-tert-butyl 1-(5-bromo-3-(3-fluoro-4-methoxybenzamido)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-ylcarbamate (120 mg, 27% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08758830B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-3d1b6dfe5ff94c21913b13e06bd09b8b
출처 메모uspto-grants-2014_06