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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406251Generated: October 31, 2026

Potassium Carbonate → 3-Phenyl-2-p-tolylpyrido[2,3-b]pyrazine

https://huagongshe.com/reaction/406251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTolylboronic acidHCID 79799—
Reactant2-Chloro-3-phenylpyrido[2,3-b]pyrazineHCID 86681858—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-Phenyl-2-p-tolylpyrido[2,3-b]pyrazineHCID 59090400—

Reaction Steps

2-Chloro-3-phenylpyrido[2,3-b]pyrazine (step 3) (175 mg, 0.724 mmol) in dry dioxane (4 ml) under nitrogen was treated with p-tolylboronic acid (108 mg, 0.797 mmol), potassium carbonate (200 mg, 1.448 mmol) in water (0.5 ml) and tetrakis(triphenylphosphine)palladium(0) (41.8 mg, 0.036 mmol). The resulting mixture was heated using microwave radiation at 150° C. for 1 hour. After cooling to RT, the mixture was diluted with water (100 ml) and extracted with DCM (×3). The combined organic extracts were washed with brine, dried over MgSO4 and filtered. The solvent was removed in vacuo and the crude product was purified by chromatography on silica eluting with 0-30% EtOAc/iso-hexane to afford the title compound as a yellow solid; LCMS; Rt 1.19 mins MS m/z 298 [ M+H]+; Method 2minLC_v003

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754085B2
Source datasetuspto-grants-2014_06
ORD IDord-0fe3e16955694dee9ae773eb2d2c9e34
Source noteuspto-grants-2014_06