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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734149Generated: October 31, 2026

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

https://huagongshe.com/reaction/1734149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Bis-trifluoromethylphenylboronic acidHCID 156265—
Reactant3-Amino-6-bromopyrazine-2-carbonitrileHCID 11052611—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
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(O) 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 numberUS05532367
Source datasetuspto-grants-1996_07
ORD IDord-0decac49becc4f6ab0ae9d299ace4bed
Source noteuspto-grants-1996_07