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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(1-Hydroxybutyl)-7-methoxy-2-trifluoromethyl-pyrazolo[1,5-a]pyridine | HCID 59389279 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Butyryl-7-methoxy-2-trifluoromethyl-pyrazolo[1,5-a]pyridine | HCID 59389394 | 66.1% |
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
| 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-7c745f4da862410ab76466744116329d |
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| Source note | uspto-grants-2010_07 |
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