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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 712754생성일: 2026년 10월 23일

Pyridine → 1-[2-(5-Bromo-pyridin-3-yl)-pyrrolidin-1-yl]-ethanone

https://huagongshe.com/ko/reaction/712754

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Acetic AnhydrideHCID 7918—
반응물3-Bromo-5-(pyrrolidin-2-yl)pyridineHCID 4403815—
용매DichloromethaneHCID 6344—
생성물1-[2-(5-Bromo-pyridin-3-yl)-pyrrolidin-1-yl]-ethanoneHCID 117667240132%

반응 단계

To a solution of 3-bromo-5-(2-pyrrolidinyl)pyridine (200 mg, 0.881 mmol) and pyridine (0.2 mL, 1.96 mmol) in DCM (1 mL) in a 8-mL vial is added acetic anhydride (0.093 mL, 0.969 mmol) dropwise. The mixture is stirred at room temperature for 2.5 h. The mixture is concentrated. The resulting crude product is purified by normal phase chromatography using 0-4.5% MeOH in DCM as the gradient to afford 1-[2-(5-bromo-pyridin-3-yl)-pyrrolidin-1-yl]-ethanone (313 mg, 83% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181272B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-621fe542518d4dd4a7d446037a497fb3
출처 메모uspto-grants-2015_11