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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710676Generated: October 25, 2026

Sodium Carbonate → 6-(3-Fluorophenyl)pyrazin-2-amine

https://huagongshe.com/reaction/1710676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Amino-6-ChloropyrazineHCID 118458—
Reactant3-Fluorophenylboronic acidHCID 2733986—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product6-(3-Fluorophenyl)pyrazin-2-amineHCID 4578834295.6%

Reaction Steps

To a stirred solution of 2-amino-6-chloropyrazine (2.0 g, 15.43 mmol) in a mixture of toluene (90 mL) and ethanol (8.5 mL) was added 3-fluorophenyl boronic acid (2.60 g, 18.51 mmol) and a 2M aqueous solution of sodium carbonate (16.2 mL, 32.40 mmol). The mixture was subjected to three cycles of evacuation-backfilling with argon, and tetrakis(triphenylphosphine)palladium (0.713 g, 0.617 mmol) was added. The mixture was subjected again to three cycles of evacuation-backfilling with argon the flask was capped and placed in a 110° C. oil bath. After 4 h, the mixture was cooled, partitioned between dichloromethane and water the organic layer was washed with brine, dried (MgSO4) and evaporated. The residue was purified by silica gel flash chromatography (33% ethyl acetate in hexanes to 50% ethyl acetate in hexanes). Concentration in vaccuo of the product-rich fractions provided the titled compound (2.79 g, 95%) as a yellowish solid (2.79 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790728B2
Source datasetuspto-grants-2010_09
ORD IDord-7050240071ad40968653655cc854aedb
Source noteuspto-grants-2010_09