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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966129Generated: October 30, 2026

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

https://huagongshe.com/reaction/1966129

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 solution of 2.1 g (38 mmol) of KOH in 20 ml of water and then 6.7 g (30 mmol) of 1-aminopyridinium iodide are added to a solution of 2.5 g (15 mmol) of ethyl 4,4,4-trifluorobut-2-ynoate in 25 ml of dichloromethane. After stirring at ambient temperature for 5 h, water is added and the reaction medium is extracted with dichloromethane. The organic phase is washed with water, dried over magnesium sulfate. filtered and concentrated. The residue obtained is purified by chromatography on silica gel, elution being carried out with an 8/2 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 numberUS08420632B2
Source datasetuspto-grants-2013_04
ORD IDord-585c0362fa2843dfaf65763584904588
Source noteuspto-grants-2013_04