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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357901Generated: October 31, 2026

4-Hydroxymethyl-7-iodo-2-trifluoromethylpyrazolo[1,5-a]pyridin → 2-Trifluoromethyl-4-formyl-7-iodo-pyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/2357901

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxymethyl-7-iodo-2-trifluoromethylpyrazolo[1,5-a]pyridinHCID 59389356—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product2-Trifluoromethyl-4-formyl-7-iodo-pyrazolo[1,5-a]pyridineHCID 5938929991.6%

Reaction Steps

The compound of Example 112 (3.26 g) was dissolved in dichloromethane (50.0 mL). To this solution, activated manganese dioxide (8.29 g) was added and the mixture was stirred at room temperature for 14 hours. Subsequently, the reaction mixture was filtered through Celite and the filtrate was evaporated. Purification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=4:1) afforded the title compound as a yellow powder (2.97 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763617B2
Source datasetuspto-grants-2010_07
ORD IDord-c6d8234b0c7f48da8c6cc899aff1e09b
Source noteuspto-grants-2010_07