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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576890Generated: November 3, 2026

Potassium Cyanide → 5-Amino-3-chloropyrazine-2-carbonitrile

https://huagongshe.com/reaction/576890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant5-Bromo-6-chloropyrazin-2-amineHCID 18180207—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Catalyst18-Crown-6HCID 28557—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-Amino-3-chloropyrazine-2-carbonitrileHCID 2107539282%

Reaction Steps

A mixture of 5-bromo-6-chloropyrazin-2-amine (1.00 g, 4.8 mmol), copper (I) iodide (914 mg, 4.8 mmol), 18-crown-6 (95 mg, 0.36 mmol) and tetrakis(triphenylphosphine)palladium (0) (83 mg, 0.072 mmol) was suspended in dry DMF (20 mL) and a stream of nitrogen was passed through for 5 minutes. Potassium cyanide (312 mg, 4.8 mmol) was added and the mixture was stirred at room temperature for 30 minutes, then refluxed at 200° C. for 3 hours. The mixture was cooled, diluted with EtOAc and absorbed onto silica gel (10 g). DMF was removed by evaporation. The product was purified by flash chromatography, eluting with 1:1 EtOAc-hexanes, to yield 5-amino-3-chloropyrazine-2-carbonitrile as a yellow solid (607 mg, 3.93 mmol, 82% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040540B2
Source datasetuspto-grants-2015_05
ORD IDord-6c279f6b506646d4b9b78aaedd593045
Source noteuspto-grants-2015_05