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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357909Generated: October 31, 2026

2-Trifluoromethyl-4-(1-hydroxyethyl)-7-methoxy-pyrazolo[1,5-a]pyridine → 4-Acetyl-2-trifluoromethyl-7-methoxy-pyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/2357909

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Trifluoromethyl-4-(1-hydroxyethyl)-7-methoxy-pyrazolo[1,5-a]pyridineHCID 59389323—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product4-Acetyl-2-trifluoromethyl-7-methoxy-pyrazolo[1,5-a]pyridineHCID 5938934566.4%

Reaction Steps

The compound of Example 134 (1.64 g) was dissolved in dichloromethane (30.0 mL). To this solution, activated manganese dioxide (5.48 g) was added and the mixture was stirred at room temperature for 16 hours. Subsequently, a second portion of activated manganese dioxide (5.48 g) was added and the mixture was stirred at room temperature for 10 hours. A third portion of activated manganese dioxide (5.48 g) was then added and the mixture was stirred at room temperature for 10.5 hours. Finally, a fourth portion of activated manganese dioxide (2.74 g) 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 (1.08 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763617B2
Source datasetuspto-grants-2010_07
ORD IDord-b3886fbdbb674471b20ea1513c25a78b
Source noteuspto-grants-2010_07