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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634084Generated: October 31, 2026

2-Chloro-4-cyanopyridine → HCID 18677150, compound

https://huagongshe.com/reaction/1634084

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-cyanopyridineHCID 568638—
Reactant4-(3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl)anilineHCID 2740668—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 18677150HCID 1867715054.8%

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 1-(4′-aminophenyl)-3,5-bis(trifluoromethyl)pyrazole (0.36 g) and 2-chloro-4-cyanopyridine (0.14 g) in dioxane (1 mL) was heated at 125° C. in a sealed tube for 5 days. The mixture was diluted with ethyl acetate and washed with water. The organic phase was dried, filtered and evaporated. Chromatography of the residue over silica gel (methylene chloride to 2% ethanol/methylene chloride gradient gave the above-named compound (0.22 g) mp 152-153° C. NMR (CDCl3) 8.45 (1H, m), 7.86 (3H, m), 7.48 (2H, d), 7.20 (1H, br s), 7.07 (1H, s), 6.91 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506747B1
Source datasetuspto-grants-2003_01
ORD IDord-75206f775d2343318e1bbd2630cf48e5
Source noteuspto-grants-2003_01