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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926772Generated: October 31, 2026

Sodium Carbonate → 5-[3-(Trifluoromethyl)phenyl]pyrazin-2-amine

https://huagongshe.com/reaction/926772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Amino-5-bromopyrazineHCID 599539—
Reactant3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-[3-(Trifluoromethyl)phenyl]pyrazin-2-amineHCID 20567072—

Reaction Conditions

Temperature135 °C

Reaction Steps

Into a 500-mL sealed tube purged and maintained with an inert atmosphere of nitrogen, was placed 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), 3-(trifluoromethyl)phenylboronic acid (4.46 g, 23.48 mmol, 1.02 equiv), a solution of sodium carbonate (4.88 g, 46.04 mmol, 2.00 equiv) in water (23 mL), and Pd(PPh3)4 (532 mg, 0.46 mmol, 0.02 equiv). The resulting solution was stirred overnight at 135° C. in an oil bath. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column and eluted with ethyl acetate/petroleum ether (1:5). This resulted in 4.4 g (80%) of 5-(3-(trifluoromethyl)phenyl)pyrazin-2-amine as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09289429B2
Source datasetuspto-grants-2016_03
ORD IDord-4196e923c74f44a59b9eaeac57e25f54
Source noteuspto-grants-2016_03