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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874552Generated: October 25, 2026

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

https://huagongshe.com/reaction/1874552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAcetyl chlorideHCID 6367—
ReactantSodium CarbonateHCID 10340—
ReactantN-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-3-methylpyridine-2-carboxamideHCID 57749390—
SolventTetrahydrofuranHCID 8028—
SolventDimethylacetamideHCID 31374—
SolventSodium BicarbonateHCID 516892—
ProductN-(3-{[2-(acetylamino)imidazo[1,2-a]pyridin-6-yl]oxy}phenyl)-3-methylpyridine-2-carboxamideHCID 5774919349.3%

Reaction Steps

To a solution of N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-3-methylpyridine-2-carboxamide (130 mg, 0.362 mmol) in N,N-dimethylacetamide (5 mL) was added acetyl chloride (26.0 μL, 0.366 mmol), and the mixture was stirred at room temperature for 3 hr. Methanol, tetrahydrofuran and aqueous sodium carbonate solution were added to the reaction mixture, and the mixture was stirred at 60° C. for 68 hr. The reaction mixture was 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 (71.7 mg, 49%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-101cbe45f43742ebb77df4d278282f2e
Source noteuspto-grants-2012_11