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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874538Generated: October 25, 2026

Methanol → 3-methyl-N-(3-{[2-(propanoylamino)imidazo[1,2-a]pyridin-6-yl]oxy}phenyl)pyridine-2-carboxamide

https://huagongshe.com/reaction/1874538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium CarbonateHCID 10340—
ReactantPropionyl chlorideHCID 62324—
ReactantN-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-3-methylpyridine-2-carboxamideHCID 57749390—
SolventTetrahydrofuranHCID 8028—
SolventDimethylacetamideHCID 31374—
Product3-methyl-N-(3-{[2-(propanoylamino)imidazo[1,2-a]pyridin-6-yl]oxy}phenyl)pyridine-2-carboxamideHCID 5774919741.2%

Reaction Steps

To a solution of N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-3-methylpyridine-2-carboxamide (129 mg, 0.359 mmol) in N,N-dimethylacetamide (6 mL) was added propionylchloride (34.3 μL, 0.395 mmol), and the mixture was stirred at room temperature for 22 hr. Methanol, tetrahydrofuran and aqueous sodium carbonate solution were added to the reaction mixture, and the mixture was stirred at 60° C. for 22 hr. The reaction mixture was concentrated under reduced pressure, diluted with aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate. The organic layer was washed with aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (0%→100% ethyl acetate-hexane) to give the title compound (61.4 mg, 41%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-7c52e50d50fd407e8041e6539316fd7a
Source noteuspto-grants-2012_11