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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 613617생성일: 2026년 10월 24일

Pyridine → 8-Acetoxy-2-methylimidazo[1,2-a]pyridine

https://huagongshe.com/ko/reaction/613617

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Acetic AnhydrideHCID 7918—
반응물2-Methylimidazo[1,2-a]pyridin-8-olHCID 820953—
용매DichloromethaneHCID 6344—
생성물8-Acetoxy-2-methylimidazo[1,2-a]pyridineHCID 18321926102%

반응 단계

A mixture of 8-hydroxy-2-methylimidazo[1,2-a]pyridine (10 g), acetic anhydride (10.3 g) and pyridine (10.7 g) in anhydrous dichloromethane (100 ml) was stirred for 1 hour at ambient temperature and allowed to stand overnight. The 30 mixture was washed with water, and the organic layer was separated. The aqueous layer was neutralized with sodium bicarbonate and extracted with chloroform. The combined organic layers were washed with saturated sodium bicarbonate solution, dried over magnesium sulfate and evaporated in vacuo to give 8-acetoxy-2-methylimidazo[1,2-a]pyridine (13.1 g) as oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06008229
출처 데이터셋uspto-grants-1999_12
ORD IDord-c73c14e2cff948938980e69f1e0397eb
출처 메모uspto-grants-1999_12