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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392335Generated: October 29, 2026

Hydrochloric Acid → 6-Chloro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile

https://huagongshe.com/reaction/392335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantThiophenolHCID 7969—
ReactantPotassium CarbonateHCID 11430—
Reactant3,6-Dichloropyrazine-2-carbonitrileHCID 22662845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-Chloro-3-(phenylsulfanyl)-2-pyrazinecarbonitrileHCID 22662804—

Reaction Conditions

Temperature40 °C

Reaction Steps

In 50 mL of N,N-dimethylformamide was dissolved 10.0 g of 3,6-dichloro-2-pyrazinecarbonitrile. After adding 6.49 mL of thiophenol and 11.91 g of potassium carbonate successively, the mixture thus obtained was stirred at 40° C. for 3 hours. The reaction mixture was poured into a mixture of 100 mL of ethyl acetate and 100 mL of water, and pH was adjusted to 2 with 6 mol/L hydrochloric acid. The organic layer was separated, washed successively with water and saturated aqueous solution of sodium chloride, and dried on anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent: toluene:n-hexane=1:3] to obtain 3.80 g of 6-chloro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile as a light yellow-colored oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800629B2
Source datasetuspto-grants-2004_10
ORD IDord-a144a20ceaec43b280990f5f7eafb94f
Source noteuspto-grants-2004_10