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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73503생성일: 2026년 10월 23일

3-Methylpyridine → (2S,5R)-6-benzyloxy-7-oxo-1,6-diaza-bicyclo[3.2.1]octane-2-carboxylic acid benzyl ester

https://huagongshe.com/ko/reaction/73503

반응식

참여 물질

역할이름HCID투입량
반응물3-MethylpyridineHCID 7970—
반응물TriphosgeneHCID 94429—
반응물Sodium BicarbonateHCID 516892—
반응물Benzyl (2S,5R)-5-((benzyloxy)amino)piperidine-2-carboxylate oxalateHCID 70673933—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물(2S,5R)-6-benzyloxy-7-oxo-1,6-diaza-bicyclo[3.2.1]octane-2-carboxylic acid benzyl esterHCID 57389438—

반응 조건

온도0 °C

반응 단계

3-picoline (45 ml, 464, 4 eq) was added to a slurry of benzyl (2S,5R)-5-[(benzyloxy)amino]piperidine-2-carboxylate ethanedioate (50 g, 116 mmol, 1 eq) in dichloromethane (1000 ml) at 0° C., followed by a solution of triphosgene (31.0 g, 104.4 mmol, 0.9 eq) in dichloromethane (200 ml). The mixture was stirred at 0° C. until the reaction was deemed to be complete. The reaction was quenched with a solution of sodium bicarbonate (24.4 g, 290 mmol, 2.5 eq) in water (300 ml), and the layers were separated. The aqueous layer was extracted with dichloromethane (100 ml) and the combined organic layers were washed with water. The organic layer was concentrated in vacuo to give (2S,5R)-6-benzyloxy-7-oxo-1,6-diaza-bicyclo[3.2.1]octane-2-carboxylic acid benzyl ester as a solution in dichloromethane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829191B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-338dc3c7bae043a6b4044df29382baec
출처 메모uspto-grants-2014_09