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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723992Generated: October 29, 2026

HCID 22174848, compound → 1-[2-(4-Fluorophenyl)-6-(trifluoromethyl)pyrazolo[1,5-a]pyridin-3-yl]-2-propyn-1-one

https://huagongshe.com/reaction/723992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22174848HCID 22174848—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product1-[2-(4-Fluorophenyl)-6-(trifluoromethyl)pyrazolo[1,5-a]pyridin-3-yl]-2-propyn-1-oneHCID 2217484169%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (0° C.) solution of 1-[2-(4-fluorophenyl)-6-(trifluoromethyl)pyrazolo[1,5-α]pyridin-3-yl]-2-propyn-1-ol (5.00 g, 15.0 mmol) in chloroform (400 mL) was added manganese dioxide (130 g, 1.50 mol). The reaction mixture was stirred at 0° C. for 1.5 hours. The reaction mixture was filtered through a pad of Celite. The filtrate was concentrated in vacuo to provide 1-[2-(4-fluorophenyl)-6-(trifluoromethyl)pyrazolo[1,5-α]pyridin-3-yl]-2-propyn-1-one (3.44 g, 690/%) as a clear oil. Rf 0.39 (4:1 hexanes:ethyl acetate); 1H NMR (400 MHz, CDCl3) δ 8.90 (s, 1H), 8.61 (d, 1H), 7.72–7.69 (m, 3H), 7.17 (m, 2H), 3.06 (s, 1H); MS m/333 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141569B2
Source datasetuspto-grants-2006_11
ORD IDord-4e1e2b3427f747a7a1f398931dc82272
Source noteuspto-grants-2006_11