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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879334Generated: October 27, 2026

Potassium Carbonate → 6-(3-bromophenyl)-1-methyl-1H-pyrazolo[4,3-b]pyridine

https://huagongshe.com/reaction/879334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Bromophenyl)boronic acidHCID 2734318—
Reactant6-Bromo-1-methyl-1H-pyrazolo(4,3-b)pyridineHCID 40152261—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product6-(3-bromophenyl)-1-methyl-1H-pyrazolo[4,3-b]pyridineHCID 86699853—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 6-bromo-1-methyl-1H-pyrazolo[4,3-b]pyridine (120 mg, 0.566 mmol) and 3-bromophenylboronic acid (136 mg, 0.679 mmol) in degassed 1,4-dioxane (6 mL) and water (2 mL) was added K2CO3 (391 mg, 2.83 mmol) and tetrakis(triphenylphosphine)palladium(0) (32 mg, 0.028 mmol). The reaction mixture was heated at 90° C. for 1 h, cooled and partitioned between ethyl acetate and brine. The organic layer was separated, dried over Na2SO4 and concentrated to give crude which was purified by chromatographic column to afford the desired product. LCMS-ESI+: calc'd for C13H10BrN3: 288.01 (M+H+); Found: 288.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987250B2
Source datasetuspto-grants-2015_03
ORD IDord-47c6628427564d20818fd5f6ec3567dc
Source noteuspto-grants-2015_03