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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392348Generated: October 30, 2026

Potassium Fluoride → HCID 22662803, compound

https://huagongshe.com/reaction/392348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
ReactantHCID 22662786HCID 22662786—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 22662803HCID 22662803—

Reaction Conditions

Temperature70 °C

Reaction Steps

In 10.5 mL of dimethyl sulfoxide was dissolved 0.35 g of t-butyl 5-bromo-3-cyano-2-pyrazinylcarbamate. After adding 0.17 g of potassium fluoride, the mixture was stirred first at 70° C. for 30 minutes and then at 90° C. for 30 minutes to form t-butyl 3-cyano-5-fluoro-2-pyrazinylcarbamate in the reaction system. Then, 0.17 g of potassium fluoride was added and stirred at 90° C. for 40 minutes. The reaction mixture was returned to room temperature and added to a mixture of 30 ml of ethyl acetate and 60 mL of water, pH was adjusted to 8 with saturated aqueous solution of sodium hydrogen carbonate, and the organic layer was separated. The organic layer thus obtained was washed with saturated aqueous solution of sodium chloride and dried on anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent: n-hexane:ethyl acetate=3:1] to obtain 20 mg of 3-amino-6-fluoro-2-pyrazinecarbonitrile as a yellow-colored solid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800629B2
Source datasetuspto-grants-2004_10
ORD IDord-cc6613561daf4791b3d49a6cbf55e692
Source noteuspto-grants-2004_10