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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517524Generated: October 31, 2026

Potassium Hydroxide → Ethyl 2-trifluoromethylpyrazolo[1,5-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/517524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantPyridinium, 1-amino-, iodide (1:1)HCID 2733704—
ReactantEthyl 4,4,4-trifluoro-2-butynoateHCID 3597254—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-trifluoromethylpyrazolo[1,5-a]pyridine-3-carboxylateHCID 6808869073%

Reaction Steps

A mixture of 2.1 g (37.6 mmol) of potassium hydroxide and 6.7 g (30.1 mmol) of aminopyridinium iodide in 20 ml of water is added to a solution of 2.5 g (15.1 mmol) of ethyl 4,4,4-trifluorobut-2-ynoate in 25 ml of dichloromethane. After stirring for 5 h at ambient temperature, water is added and the mixture is extracted with dichloromethane. The organic phase is washed with water, dried over magnesium sulphate, filtered and concentrated to dryness. The crude product is purified by chromatography over silica gel eluted with an 80/20 heptane/ethyl acetate mixture. 2.8 g (73%) of ethyl 2-trifluoromethylpyrazolo[1,5-a]pyridine-3-carboxylate are obtained in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115102B2
Source datasetuspto-grants-2015_08
ORD IDord-4055962cdfa54e37a3ec4013ba50657f
Source noteuspto-grants-2015_08