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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant1-(3-Chloro-4-fluorophenyl)-2-(5-trifluoromethyl-2-pyridinyl)ethanone oximeHCID 86590213—
CatalystFerrous ChlorideHCID 24458—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(3-Chloro-4-Fluorophenyl)-6-Trifluoromethylpyrazolo[1,5-a]PyridineHCID 983651382%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756498B2
Source datasetuspto-grants-2004_06
ORD IDord-1dd045f479544b50a7a8b9d36dbf514f
Source noteuspto-grants-2004_06