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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357910Generated: November 2, 2026

4-(1-Hydroxybutyl)-7-methoxy-2-trifluoromethyl-pyrazolo[1,5-a]pyridine → 4-Butyryl-7-methoxy-2-trifluoromethyl-pyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/2357910

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1-Hydroxybutyl)-7-methoxy-2-trifluoromethyl-pyrazolo[1,5-a]pyridineHCID 59389279—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product4-Butyryl-7-methoxy-2-trifluoromethyl-pyrazolo[1,5-a]pyridineHCID 5938939466.1%

Reaction Steps

The compound of Example 136 (265 mg) was dissolved in dichloromethane (5.00 mL). To this solution, activated manganese dioxide (801 mg) was added and the mixture was stirred at room temperature for 16 hours. Subsequently, a second portion of activated manganese dioxide (801 mg) was added and the mixture was stirred at room temperature for 10 hours. A third portion of activated manganese dioxide (801 mg) was then added and the mixture was stirred at room temperature for 10.5 hours. Finally, a fourth portion of activated manganese dioxide (400 mg) was added and the mixture was stirred for 13.5 hours. Subsequently, the reaction mixture was filtered through Celite and the filtrate was evaporated to afford the title compound as a pale yellow powder (174 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763617B2
Source datasetuspto-grants-2010_07
ORD IDord-7c745f4da862410ab76466744116329d
Source noteuspto-grants-2010_07