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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74490생성일: 2026년 10월 24일

Water → Benzyl 4-(2-oxo-2,3-dihydro-imidazo[4,5-b]pyridin-1-yl)-piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/74490

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1,4-Bis(diphenylphosphino)butaneHCID 82124—
반응물Sodium BicarbonateHCID 516892—
반응물Benzyl 4-[1-(2-chloro-pyridin-3-yl)-ureido]-piperidine-1-carboxylateHCID 46853854—
촉매palladium(II) acetateHCID 167845—
용매2-Methyl-2-butanolHCID 6405—
생성물Benzyl 4-(2-oxo-2,3-dihydro-imidazo[4,5-b]pyridin-1-yl)-piperidine-1-carboxylateHCID 46853855—

반응 조건

온도35 °C

반응 단계

1108 g (2.85 mol) benzyl 4-[1-(2-chloro-pyridin-3-yl)-ureido]-piperidine-1-carboxylate were refluxed with 720 g (8.57 mol) sodium hydrogen carbonate in 14.5 L tert-amylalcohol. 3 L of solvent were distilled off. The reaction mixture was cooled to 35° C. and mixed with 11 mL water. Then 13 g (0.058 mol) palladium acetate and 49 g (0.115 mol) 1,4-bis-(diphenylphosphino)-butane (DPPB) were added and the mixture was refluxed. It was stirred at 100° C. until the reaction was complete, cooled to RT and 7.5 L water were added. The organic phase was separated off, washed with 5 L water and then evaporated down. The oily residue was twice combined with 3 L isopropyl acetate and distilled off. Then the residue was dissolved hot in 7 L isopropyl acetate and slowly cooled to ambient temperature. The solid that crystallised out was suction filtered, washed with 2 L isopropyl acetate and tert.-butyl-methylether and dried at 50° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829006B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b139f2a6a9814fcd9c7fa62ffd18c626
출처 메모uspto-grants-2014_09