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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205732Generated: November 1, 2026

Sodium Carbonate → 6-(3-Fluoro-4-(trifluoromethoxy)phenyl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyridine

https://huagongshe.com/reaction/2205732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-2-fluoro-1-(trifluoromethoxy)benzeneHCID 2782217—
Reactant3-(Trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyridin-6-ylboronic acidHCID 58118915—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product6-(3-Fluoro-4-(trifluoromethoxy)phenyl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyridineHCID 86650229—

Reaction Conditions

Temperature110 °C

Reaction Steps

3-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyridin-6-ylboronic acid (56.2 mg, 0.217 mmol), 4-bromo-2-fluoro-1-(trifluoromethoxy)benzene (50.0 mg, 0.217 mmol, 1.0 equiv.) and Pd(PPh3)4 (12.6 mg, 0.0109 mmol, 0.05 equiv.) was placed in a 50 mL round bottomed flask under a nitrogen atmosphere. To the flask were added 2M-Na2CO3 (1.0 mL, 2.0 mmol) and DMF (4 mL) subsequently at ambient temperature. The mixture was heated at 110° C. for 1 hours. The mixture was filtered through Celite (3 g) and the Celite was washed with EtOAc (70 mL). The organic layer was washed with brine (30 mL) and dried with Na2SO4. The solvent was removed under a reduced pressure. Obtained crude mixture was purified by a column chromatography (SiO2=25 g, EtOAc/hexane=1:3 to 1:1, Rf=0.3 with EtOAc/hexane=1:1) to give 6-(3-fluoro-4-(trifluoromethoxy)phenyl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyridine as colorless crystals

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371329B2
Source datasetuspto-grants-2016_06
ORD IDord-f00a47c2c58a4e8b92b7d7a53341e60d
Source noteuspto-grants-2016_06