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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2112387Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2112387

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Bromomethoxy)ethyl acetateHCID 367656—
EduktPotassium tert-butoxideHCID 23665647—
EduktHCID 178420746HCID 178420746—
LösungsmittelDimethylformamideHCID 6228—
Produktacetic acid 2-(3H-imidazo[4,5-b]pyridin-3-ylmethoxy)-ethyl esterHCID 6887999841%

Reaktionsschritte

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]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07524823B2
Quelldatensatzuspto-grants-2009_04
ORD IDord-d630aad3c925412699f1721b1e0b125c
Quellennotizuspto-grants-2009_04