Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747858Generated: October 25, 2026

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

https://huagongshe.com/reaction/747858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
Reactant5-methyl-3-phenyl-N-(pyridin-2-ylmethyl)-1,2-oxazole-4-carboxamideHCID 700862—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
Product3-(5-Methyl-3-phenyl-isoxazol-4-yl)-imidazo[1,5-a]pyridineHCID 1621489547.2%

Reaction Steps

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]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399769B2
Source datasetuspto-grants-2008_07
ORD IDord-4228684736b64a7aa6320801e1172ff2
Source noteuspto-grants-2008_07