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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101360Generated: October 30, 2026

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

https://huagongshe.com/reaction/2101360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
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-methoxyphenyl)-2-isobutyl-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-oneHCID 5779942419.2%

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-methoxyphenylboronic 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 20 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 (10 mg, 0.025 mmol) as a pale yellow solid. MS: [M+H]+=404.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572808B2
Source datasetuspto-grants-2009_08
ORD IDord-319628f0e2c449de84a3e7c7c6f6bece
Source noteuspto-grants-2009_08