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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Trifluoromethyl-4-(1-hydroxyethyl)-7-methoxy-pyrazolo[1,5-a]pyridine | HCID 59389323 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Acetyl-2-trifluoromethyl-7-methoxy-pyrazolo[1,5-a]pyridine | HCID 59389345 | 66.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763617B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-b3886fbdbb674471b20ea1513c25a78b |
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| Source note | uspto-grants-2010_07 |
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