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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 277011Erstellt: 26. Oktober 2026

Methanol → 2-Furan-2-yl-7-pyridin-4-yl-[1,2,4]triazolo [1,5-a]pyridin-5-ylamine

https://huagongshe.com/reaction/277011

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktSodium hydrideHCID 24758—
Edukt3-Pyridin-4-YL-acrylonitrileHCID 53407808—
Edukt3-benzenesulfonyl-methyl-5-furan-2-yl-1H-[1,2,4]triazoleHCID 70170246—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Furan-2-yl-7-pyridin-4-yl-[1,2,4]triazolo [1,5-a]pyridin-5-ylamineHCID 988208113%

Reaktionsschritte

To a boiling suspension of 5.9 g(0.12 mol) sodiumhydride (55%) in 100 ml tetrahydrofuran was slowly added over a period of 6 hours a mixture of 10.1 g (0.035 mol) 3-benzenesulfonyl-methyl-5-furan-2-yl-1H-[1,2,4]triazole and 4.56 g (0.035 mol) 3-(4-pyridinyl)-2-propenenitrile in 400 ml tetrahydrofuran. Boiling was continued for 15 hours and then 50 ml methanol were added at room temperature. Evaporation of the solvent and chromatography on silicagel with dichloromethane/methanol 95/5 gave 1.3 g (13%) 2-furan-2-yl-7-pyridin-4-yl-[1,2,4]triazolo [1,5-a]pyridin-5-ylamine as yellow crystals with mp. 294-296° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06355653B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-c380808d2e1f4b5990ee50f4ac7eebb4
Quellennotizuspto-grants-2002_03