HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354245Generated: October 26, 2026
Water → 2-(3-Chloro-4-Fluorophenyl)-6-Trifluoromethylpyrazolo[1,5-a]Pyridine
https://huagongshe.com/reaction/354245
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 1-(3-Chloro-4-fluorophenyl)-2-(5-trifluoromethyl-2-pyridinyl)ethanone oxime | HCID 86590213 | — |
| Catalyst | Ferrous Chloride | HCID 24458 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-(3-Chloro-4-Fluorophenyl)-6-Trifluoromethylpyrazolo[1,5-a]Pyridine | HCID 9836513 | 82% |
Reaction Steps
To a suspension of 1-(3-chloro-4-fluorophenyl)-2-(5-trifluoromethyl-2-pyridinyl)ethanone oxime (15.56 g, 46.8 mmol) in DME (64 ml) at 5° C. was added TFAA (6.6 ml, 46.8 mmol) and the mixture stirred for 10 minutes. Triethylamine (19.6 ml, 140.4 mmol) was then added dropwise over 15 min. After the addition was complete, the reaction was then warmed to room temperature. After stirring for 1 hour, iron (II) chloride (60 mg) was added and the mixture was then heated to 75° C. for 1 hour then allowed to cool. The mixture was poured into water (500 ml) and extracted with dichloromethane (300 ml). The organic extracts were dried over MgSO4 and concentrated under reduced pressure to ca. 50 ml. This residue was purified by filtration through a layer of silica gel washing with further dichloromethane. The filtrate was concentrated to dryness to give 12 g (82%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06756498B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-1dd045f479544b50a7a8b9d36dbf514f |
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| Source note | uspto-grants-2004_06 |
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