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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5441Erstellt: 23. Oktober 2026

Formaldehyde → 5-[2-(Methylsulfonylamino)ethylthio]3-morpholinomethylimidazo[1,2-a]pyridine

https://huagongshe.com/de/reaction/5441

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktMorpholineHCID 8083—
Edukt5-[2-(Methylsulfonylamino)ethylthio]imidazo[1,2-a]pyridineHCID 15229363—
LösungsmittelAcetic AcidHCID 176—
Produkt5-[2-(Methylsulfonylamino)ethylthio]3-morpholinomethylimidazo[1,2-a]pyridineHCID 2336285171,5%

Reaktionsschritte

To a solution of 37% formalin (178 mg, 2.2 mmoles) in acetic acid (2 ml) was added morpholin (192 μl, 2.2 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. 5-[2-(methylsulfonylamino)ethylthio] imidazo[1,2-a]pyridine (543 mg, 2 mmoles) was added to the reaction mixture, followed by stirring at 60° C. for 2 hours. After the solvent was distilled off, the residue was dissolved in chloroform (50 ml) and washed with 1N NaOH (10 ml). Then, the aqueous layer was extracted with chloroform (30 ml×3) and the combined chloroform layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:10→1:5) to obtain 530 mg of the desired product (71.5%, colorless solid).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244908
Quelldatensatzuspto-grants-1993_09
ORD IDord-1c9d4fa8cda74077a9d8cdb9265be8ed
Quellennotizuspto-grants-1993_09