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HRID 2112387作成日:2026年10月27日

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

https://huagongshe.com/reaction/2112387

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Bromomethoxy)ethyl acetateHCID 367656—
反応物Potassium tert-butoxideHCID 23665647—
反応物HCID 178420746HCID 178420746—
溶媒DimethylformamideHCID 6228—
生成物acetic acid 2-(3H-imidazo[4,5-b]pyridin-3-ylmethoxy)-ethyl esterHCID 6887999841%

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07524823B2
出典データセットuspto-grants-2009_04
ORD IDord-d630aad3c925412699f1721b1e0b125c
出典メモuspto-grants-2009_04