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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844186Generated: October 31, 2026

Cesium carbonate → Ethyl 8-[(3-fluoropyridin-2-yl)methoxy]-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/1844186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-(Chloromethyl)-3-fluoropyridine HydrochlorideHCID 19703862—
ReactantEthyl 8-hydroxy-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylateHCID 86717883—
SolventDimethylformamideHCID 6228—
ProductEthyl 8-[(3-fluoropyridin-2-yl)methoxy]-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylateHCID 86718213—

Reaction Conditions

Temperature60 °C

Reaction Steps

15.78 g (86.7 mmol) of 2-(chloromethyl)-3-fluoropyridine hydrochloride (commercially available; additionally described in: U.S. Pat. No. 5,593,993 A1, 1997; WO2007/2181 A2, 2007) and 94.06 g (288.9 mmol) of caesium carbonate were added to 16.92 g (72.2 mmol) of ethyl 8-hydroxy-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylate from Example 87A in 956 ml of DMF. The reaction mixture was stirred at 60° C. overnight. The reaction mixture was cooled to RT and filtered, the filtercake was washed with ethyl acetate and the filtrate was concentrated. About 500 ml of water were added to the residue and the precipitated solid was filtered off and dried under high vacuum. This gave 24.1 g (93% of theory) of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946215B2
Source datasetuspto-grants-2015_02
ORD IDord-36e3aa79bf064e73a81448d376572306
Source noteuspto-grants-2015_02