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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354255Generated: October 30, 2026

Water → 2-(3,5-Dichlorophenyl)-6-Trifluoromethylpyrazolo[1,5-a]Pyridine

https://huagongshe.com/reaction/354255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant1-(3,5-Dichlorophenyl)-2-(5-trifluoromethyl-2-pyridinyl)ethanone oximeHCID 74057994—
CatalystFerrous ChlorideHCID 24458—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(3,5-Dichlorophenyl)-6-Trifluoromethylpyrazolo[1,5-a]PyridineHCID 2351334925.4%

Reaction Steps

To a suspension of 1-(3,5-dichlorophenyl)-2-(5-trifluoromethyl-2-pyridinyl)ethanone oxime (13.30 g, 38 mmol) in DME (52 ml) at 5° C. was added TFAA (6.25 ml, 44 mmol) and the mixture stirred for 10 minutes. Triethylamine (18.6 ml, 134 mmol) was then added dropwise over 15 min. After the addition was complete, the reaction mixture was then warmed to room temperature. After stirring for 1 hour, iron (II) chloride (56 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 3.2 g (25%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756498B2
Source datasetuspto-grants-2004_06
ORD IDord-96448e63c28a4714b218cbe42733735c
Source noteuspto-grants-2004_06