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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 548888Erstellt: 24. Oktober 2026

Sodium hydride → 6-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-[1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/de/reaction/548888

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt6-Chloro-[1,2,4]triazolo[4,3-b]pyridazineHCID 313624—
Edukt(5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanolHCID 2776149—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-[1,2,4]triazolo[4,3-b]pyridazineHCID 4263024951%

Reaktionsschritte

To a solution of (5-methyl-3-phenyl-isoxazol-4-yl)-methanol (100 mg, 0.53 mmol) in DMF (2 mL) was added sodium hydride (55% dispersion in mineral oil, 25.4 mg, 0.58 mmol). The mixture was stirred at room temperature for 15 min. After addition of 6-chloro-1,2,4-triazolo[4,3-b]pyridazine (90 mg, 0.58 mmol) the mixture was stirred at room temperature for another 2 h. Then the mixture was evaporated, extracted (ethyl acetate/water) and the organic phase was dried with sodium sulfate and concentrated. Chromatography (SiO2, dichloromethane:methanol=100:0 to 9:1) afforded the title compound (80 mg, 51%) as a white solid. MS: m/e=308.4 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07943619B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-92ae9d6cfb8e4f08b0f53649947e0ec7
Quellennotizuspto-grants-2011_05