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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 397553Erstellt: 23. Oktober 2026

Glycidol → 6-(2-Oxiranylmethoxy)[1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/de/reaction/397553

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktGlycidolHCID 11164—
EduktSodium hydrideHCID 24758—
Edukt6-Chloro-[1,2,4]triazolo[4,3-b]pyridazineHCID 313624—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-(2-Oxiranylmethoxy)[1,2,4]triazolo[4,3-b]pyridazineHCID 2300031632,8%

Reaktionsschritte

12.0 g of 2-oxiranylmethanol and 2.50 g of 6-chloro[1,2,4]triazolo[4,3-b]pyridazine were dissolved in 40 ml of N,N-dimethylformamide; under ice cooling, 713 mg of 60% oily sodium hydride was added, followed by stirring at room temperature for 30 minutes. After cold saline was added, the reaction mixture was extracted with ethyl acetate-tetrahydrofuran (1:1) and dried over magnesium sulfate. After concentration under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with ethyl acetate-methanol (10:1). The desired fraction was collected and concentrated under reduced pressure; the precipitated crystal was washed with diethyl ether and dried to yield 1.02 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06610694B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-8957a2a462814b4bae3c9e5dff4a92b5
Quellennotizuspto-grants-2003_08