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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 747858Erstellt: 26. Oktober 2026

Phosphorus oxychloride → 3-(5-Methyl-3-phenyl-isoxazol-4-yl)-imidazo[1,5-a]pyridine

https://huagongshe.com/reaction/747858

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphorus oxychlorideHCID 24813—
EduktSodium BicarbonateHCID 516892—
Edukt5-methyl-3-phenyl-N-(pyridin-2-ylmethyl)-1,2-oxazole-4-carboxamideHCID 700862—
LösungsmittelDichloromethaneHCID 6344—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt3-(5-Methyl-3-phenyl-isoxazol-4-yl)-imidazo[1,5-a]pyridineHCID 1621489547,2%

Reaktionsschritte

To a solution of 5-methyl-3-phenyl-isoxazole-4-carboxylic acid (pyridin-2-ylmethyl)-amide (0.293 g, 1 mmol) in dichloroethane (5 mL) was added phosphorus oxychloride (0.47 mL, 5 mmol) via a syringe and the resulting mixture heated under reflux overnight. After cooling to room temperature, the mixture was diluted with dichloromethane. Cold saturated sodium bicarbonate (15 mL) was then added slowly and the mixture was vigorously stirred for 15 min. The organic layer was separated and the aqueous was extracted with dichloromethane. The combined extracts were washed with water, dried over sodium sulphate, and evaporated. Purification by preparative HPLC on reversed phase [0.1% aq. ammonia (25%)] afforded the title compound (0.13 g, 47%) as an orange solid. MS: m/e: 276.1 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07399769B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-4228684736b64a7aa6320801e1172ff2
Quellennotizuspto-grants-2008_07