Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9180Generated: October 25, 2026

N-amino-2-(1-butynyl)pyridinium mesitylenesulfonate → 2-Ethylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/9180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-amino-2-(1-butynyl)pyridinium mesitylenesulfonateHCID 21984654—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product2-Ethylpyrazolo[1,5-a]pyridineHCID 16116261—

Reaction Steps

A 6.1 g portion of the obtained N-amino-2-(1-butynyl)pyridinium mesitylenesulfonate was dissolved in tetrahydrofuran (600 mL), potassium tert-butoxide (3.55 g) was added at room temperature, and the mixture was vigorously stirred for 30 minutes. After adding ice water to the reaction mixture, extraction was performed with ethyl acetate. The aqueous layer was again extracted with ethyl acetate, the insoluble portion was filtered with a celite filter, and the organic layers were combined and washed with brine. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (0.63 g) was obtained from the n-hexane:ethyl acetate (10:1) fraction as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091215B2
Source datasetuspto-grants-2006_08
ORD IDord-e2417cce65cb4c1590485a0406f53f9b
Source noteuspto-grants-2006_08