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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440892Generated: October 25, 2026

Water → 2-Amino-3-cyano-5-[3,5-di(trifluoromethyl)phenyl]pyrazine

https://huagongshe.com/reaction/440892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Bis-trifluoromethylphenylboronic acidHCID 156265—
Reactant3-Amino-6-bromopyrazine-2-carbonitrileHCID 11052611—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2-Amino-3-cyano-5-[3,5-di(trifluoromethyl)phenyl]pyrazineHCID 15335268—

Reaction Steps

A stirred solution of 1.6 grams (0.008 mole) of 2-amino-3-cyano-5-bromopyrazine [prepared by the method of Taylor and Ray--JOC, 52, 3997 (1987)], 3.2 grams (0.012 mole) of 3,5-di(trifluoromethyl)phenylboronic acid commercially available or prepared by the method of Thompson and Gaudino--JOC, 49, 5237 (1984)], 4.3 grams (0.031 mole) of potassium carbonate and 0.3 gram of tetrakis(triphenylphosphine)palladium(0) in 150 mL of toluene is heated at 90° C. for about 20 hours. After this time, the reaction mixture is stirred with 100 mL of water, and the organic layer is separated. The organic layer is concentrated under reduced pressure to a residue. The residue is subjected to column chromatography on silica gel. The product-containing fractions are combined and concentrated under reduced pressure, yielding 2-amino-3-cyano-5-[3,5-di(trifluoromethyl)phenyl]pyrazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521190
Source datasetuspto-grants-1996_05
ORD IDord-0daa9f0493404b04bb0ee48ace48d093
Source noteuspto-grants-1996_05