Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734159Generated: October 27, 2026

Triethylamine → 2-Amino-3-cyano-5-[(4-trifluoromethylphenyl)ethynyl]pyrazine

https://huagongshe.com/reaction/1734159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzene, 1-iodo-4-(trifluoromethyl)-HCID 67993—
Reactant2-Amino-3-cyano-5-ethynylpyrazineHCID 15335273—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product2-Amino-3-cyano-5-[(4-trifluoromethylphenyl)ethynyl]pyrazineHCID 15335274—

Reaction Steps

A solution of 3.2 grams (0.022 mole) of 2-amino-3-cyano-5-ethynylpyrazine, 8.4 grams (0.031 mole) of 4-trifluoromethylphenyl iodide, 10.7 grams (0.077 mole) of triethylamine, 0.5 gram (catalyst) of bis(triphenylphosphine)palladium(II) chloride, and 0.5 gram (catalyst) of copper iodide in 100 mL of acetonitrile is stirred at ambient temperature for about 18 hours. After this time the reaction mixture is concentrated under reduced pressure to a residue. The residue is partitioned between ethyl acetate and aqueous 1N hydrochloric acid. The two-layered mixture is filtered to remove a solid. The aqueous layer and the organic layer are separated, and the aqueous layer is washed with ethyl acetate. The ethyl acetate wash is combined with the organic layer, and the combination is washed with an aqueous solution of 10% lithium chloride. The organic layer is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residue. The residue is triturated with methylene chloride and filtered. The filtrate is subjected to column chromatography on silica gel. Elution is accomplished using methanol/methylene chloride combinations. The product-containing fractions are combined and concentrated under reduced pressure, yielding 2-amino-3-cyano-5-[(4-trifluoromethylphenyl)ethynyl]pyrazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532367
Source datasetuspto-grants-1996_07
ORD IDord-d21fb125e33d4b5c9d7d67d561300fd0
Source noteuspto-grants-1996_07