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HRID 2101300Erstellt: 26. Oktober 2026

1,1'-Carbonyldiimidazole → 8-Bromo-7-(4-chlorophenyl)[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one

https://huagongshe.com/reaction/2101300

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
Edukt3-Bromo-4-(4-chlorophenyl)-2-hydrazinylpyridineHCID 57799454—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt8-Bromo-7-(4-chlorophenyl)[1,2,4]triazolo[4,3-a]pyridin-3(2H)-oneHCID 5779943884,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Crude 3-bromo-4-(4-chlorophenyl)-2-hydrazinylpyridine (7 g, 23 mmol) was dissolved in dry THF (100 mL), and the resulting solution was cooled to 0° C. To this was added 1,1′carbonyldiimidazole (18 g, 111 mmol). The reaction mixture was stirred at room temperature for 10 h. The solvent was evaporated under vacuum, and water (10 mL) was added, which caused solid desired product to precipitate. This was filtered, washed with water (2×25 mL), and dried to obtain the title compound as a yellow solid (6.3 g), which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07572808B2
Quelldatensatzuspto-grants-2009_08
ORD IDord-f2374dc14b034ee3ace9ba8e8e5d09e1
Quellennotizuspto-grants-2009_08