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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101355Generated: October 30, 2026

Potassium Carbonate → 7,8-bis(4-chlorophenyl)-2-isobutyl-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one

https://huagongshe.com/reaction/2101355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant7-bromo-8-iodo-2-isobutyl-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-oneHCID 57799382—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product7,8-bis(4-chlorophenyl)-2-isobutyl-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-oneHCID 5779939640.8%

Reaction Conditions

Temperature200 °C

Reaction Steps

To a stirring, degassed mixture of 7-bromo-8-iodo-2-isobutyl-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one (50 mg, 0.13 mmol), 4-chlorophenylboronic acid (40 mg, 0.28 mmol), and tetrakis(triphenylphosphine)palladium (7 mg, 0.006 mmol) in dioxane (1.0 mL) at 20° C. was added K2CO3 (40 mg, 0.25 mmol) in water (0.3 mL). The resulting reaction mixture was heated in a microwave reactor at 200° C. for 10 min under argon. Analysis by HPLC/MS indicated that starting material had been consumed. The reaction mixture was brought to room temperature and was concentrated under reduced pressure. The crude product was purified by reverse phase preparative HPLC (acetonitrile-water-TFA) to isolate the title compound (22 mg, 0.053 mmol) as a light yellow solid. MS: [M+H]+=412.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572808B2
Source datasetuspto-grants-2009_08
ORD IDord-bda94cd0ae2243c5b56e8833cf3aaa4f
Source noteuspto-grants-2009_08