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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734214Generated: November 2, 2026

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

https://huagongshe.com/reaction/1734214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzene, 1-iodo-4-(trifluoromethyl)-HCID 67993—
Reactant2-Amino-3-cyano-4-methyl-5-ethynylpyridineHCID 23356702—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product2-Amino-3-cyano-4-methyl-5-[(4-trifluoromethylphenyl)ethynyl]pyridineHCID 19707204—

Reaction Steps

A solution of 1.6 grams (0.010 mole) of 2-amino-3-cyano-4-methyl-5-ethynylpyridine, 3.8 grams (0.014 mole) of 4-trifluoromethylphenyl iodide (commercially available), 3.5 grams (0.035 mole) of triethylamine, 0.3 gram (catalyst) of bis(triphenylphosphine)palladium(II) chloride, and 0.3 gram (catalyst) of copper(I)iodide in 75 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 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, yielding 2-amino-3-cyano-4-methyl-5-[(4-trifluoromethylphenyl)ethynyl]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532370
Source datasetuspto-grants-1996_07
ORD IDord-393a88828a174ff5bb84ec3f20b39fdd
Source noteuspto-grants-1996_07