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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406063Generated: October 31, 2026

Sodium Carbonate → 5-(3,4-Dimethylphenyl)pyrazin-2-amine

https://huagongshe.com/reaction/2406063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Amino-5-bromopyrazineHCID 599539—
Reactant3,4-Dimethylphenylboronic acidHCID 2734348—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-(3,4-Dimethylphenyl)pyrazin-2-amineHCID 65550074—

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of 5-bromopyrazin-2-amine (4 g, 22.99 mmol, 1.00 equiv) in 1,4-dioxane (68 mL) and methanol (23 mL) was added 3,4-dimethylphenylboronic acid (3.52 g, 23.47 mmol, 1.02 equiv), sodium carbonate (4.872 g, 45.96 mmol, 2.00 equiv) in water (23 mL), and Pd(PPh3)4 (532 mg, 0.46 mmol, 0.02 equiv) and the resulting solution was stirred for 4.5 h at 110° C. in an oil bath. The resulting mixture was concentrated under vacuum, diluted with 200 mL of ethyl acetate, washed with 2×100 mL of brine, dried over anhydrous sodium sulfate and then concentrated under vacuum. The residue was applied onto a silica gel column with petroleum ether/ethyl acetate=10:1˜1:1, then with dichloromethane/methanol (10:1˜5:1). The collected fractions were combined and concentrated under vacuum. This resulted in 4.82 g (crude) of 5-(3,4-dimethylphenyl)pyrazin-2-amine as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809339B2
Source datasetuspto-grants-2014_08
ORD IDord-f029186c36bf47b786bc3c30c7209427
Source noteuspto-grants-2014_08