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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5470Erstellt: 24. Oktober 2026

Water → 5-[2-(N-benzylmethylsulfonylamino)ethyloxy]imidazo[1,2-a]pyridine

https://huagongshe.com/de/reaction/5470

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
Edukt5-Chloroimidazo[1,2-A]pyridineHCID 10953722—
Edukt2-(N-benzylmethylsulfonylamino)-1-ethanolHCID 14947395—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-[2-(N-benzylmethylsulfonylamino)ethyloxy]imidazo[1,2-a]pyridineHCID 2336295139,4%

Reaktionsschritte

To a suspension of 60% sodium hydride in oil (0.20 g, 5 mmoles) in dimethylformamide (20 ml) was added 2-(N-benzylmethylsulfonylamino)-1-ethanol (1.14 g, 5 mmoles) with stirring under ice-cooling and the mixture was stirred at room temperature for 30 minutes. To this reaction mixture was added 5-chloroimidazo[1,2-a]pyridine (0.763 g, 5 mmoles) with stirring under ice-cooling, followed by stirring at 80° C. for 16 hours. After cooling, water was added to the reaction mixture, which was extracted with ethyl acetate and dried. After the solvent was distilled off, the residue was purified by column chromatography [eluent: ethyl acetate/hexane (1:1)→ethyl acetate/hexane (2:1)] to obtain 0.68 g of the desired product (39.4%, pale yellow oily product).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244908
Quelldatensatzuspto-grants-1993_09
ORD IDord-e3132aba721d4308b7846406e0b07587
Quellennotizuspto-grants-1993_09