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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187957Generated: November 3, 2026

Pyridine → HCID 86654452, compound

https://huagongshe.com/reaction/1187957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Amino-6-chloropyridineHCID 206246—
Reactant4-(5-(3,5-Dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl)-2-methylbenzoyl chlorideHCID 86611479—
SolventDichloromethaneHCID 6344—
ProductHCID 86654452HCID 8665445268.8%

Reaction Steps

In a solution of 0.10 g of 2-amino-6-chloropyridine and 0.16 g of pyridine in 5 mL of dichloromethane, a solution of 0.30 g of 4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-methylbenzoyl-chloride synthesized in Step 4 of Synthetic Example 1 in 5 mL of dichloromethane was added at room temperature with stirring. After the completion of the addition dropwise, it was stirred at the same temperature further for 2.5 hours. After the completion of the reaction, the solvent was distilled off under reduced pressure, the residue was dissolved in 50 mL of ethyl acetate, and precipitated insoluble material was removed through silica gel column, and the solvent was distilled off under reduced pressure. The residue was purified with silica gel column chromatography that was eluated with ethyl acetate-hexane (1:2) to obtain 0.25 g of the aimed product as colorless resinous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673951B2
Source datasetuspto-grants-2014_03
ORD IDord-7baca09a850947e3acca1bf929b7fab8
Source noteuspto-grants-2014_03