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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202202Generated: October 30, 2026

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

https://huagongshe.com/reaction/2202202

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-α]pyridine-3-carboxylate are obtained in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365529B2
Source datasetuspto-grants-2016_06
ORD IDord-da66a1a6b1ec4e888b04d8e61a2e8ca1
Source noteuspto-grants-2016_06