Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874594Generated: October 30, 2026

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

https://huagongshe.com/reaction/874594

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 numberUS08980897B2
Source datasetuspto-grants-2015_03
ORD IDord-e8f95a01418c4dc08cc0d1d2c6399112
Source noteuspto-grants-2015_03