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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389142Generated: October 30, 2026

Sodium Carbonate → 4-[5-chloro-2-(1-methyl-1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}ethoxy)phenyl]pyridine dihydrochloride

https://huagongshe.com/reaction/389142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
Reactant3-[1-(2-bromo-4-chlorophenoxy)-1-methylethyl]-4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazoleHCID 58243845—
SolventToluene-ethanol waterHCID 66602552—
Product4-[5-chloro-2-(1-methyl-1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}ethoxy)phenyl]pyridine dihydrochlorideHCID 8665302049.6%

Reaction Conditions

Temperature110 °C

Reaction Steps

Pyridin-4-ylboronic acid (26 mg), tetrakis triphenylphosphine palladium (10 mg) and sodium carbonate (156 mg) were added to a mixed solution of 3-[1-(2-bromo-4-chlorophenoxy)-1-methylethyl]-4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazole (100 mg) in toluene-ethanol-water (2 ml, 3:2:1), followed by stirring at 110° C. for 2 days. The reaction solution was concentrated under reduced pressure and diluted with chloroform. The organic layer was washed with water and saturated brine in this order and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by thin layer chromatography (ethyl acetate:methanol=98:2). The resulting solid was dissolved in ethyl acetate and 4M hydrogen chloride-ethyl acetate was added thereto, followed by stirring at room temperature for 2 hours. The precipitated crystal was collected by filtration and washed with ethyl acetate to obtain 4-[5-chloro-2-(1-methyl-1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}ethoxy)phenyl]pyridine dihydrochloride (19 mg) as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377923B2
Source datasetuspto-grants-2013_02
ORD IDord-1ba5f80a9bd247d6b57576d9a1e09fd5
Source noteuspto-grants-2013_02