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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2112387생성일: 2026년 10월 27일

2-(Bromomethoxy)ethyl acetate → acetic acid 2-(3H-imidazo[4,5-b]pyridin-3-ylmethoxy)-ethyl ester

https://huagongshe.com/reaction/2112387

반응식

참여 물질

역할이름HCID투입량
반응물2-(Bromomethoxy)ethyl acetateHCID 367656—
반응물Potassium tert-butoxideHCID 23665647—
반응물HCID 178420746HCID 178420746—
용매DimethylformamideHCID 6228—
생성물acetic acid 2-(3H-imidazo[4,5-b]pyridin-3-ylmethoxy)-ethyl esterHCID 6887999841%

반응 단계

To a solution of 1.0 g (8.39 mmol) 3H-imidazo[4,5-b]pyridine in 20 ml DMF kept under argon at 0° C. 0.94 g (8.39 mmol) potassium tert-butoxide were added. The solution was warmed to room temperature and after 1 hour a solution of 1.74 g (8.8 mmol) (2-acetoxyethoxy)methyl bromide in 5 ml DMF was added dropwise over half an hour. The reaction was stirred at room temperature for 20 hours and then poured onto 75 ml of ice water. The mixture was extracted twice with 50 ml ethyl acetate. The combined organic layers were washed with water and brine, dried over Na2SO4 filtered and concentrated in vacuo. The crude product was purified by flash chromatography (silica gel, gradient DCM, DCM/MeOH 95/5 and 9/1) to afford 0.81 g (41%) of the desired product. MS(ISP): 236.2 [MH]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07524823B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-d630aad3c925412699f1721b1e0b125c
출처 메모uspto-grants-2009_04