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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392364Generated: October 29, 2026

Water → N-(3-cyano-5-fluoro-2-pyrazinyl)benzamide

https://huagongshe.com/reaction/392364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium FluorideHCID 522689—
ReactantN-(5-bromo-3-cyano-2-pyrazinyl)benzamideHCID 22662825—
SolventDimethyl SulfoxideHCID 679—
ProductN-(3-cyano-5-fluoro-2-pyrazinyl)benzamideHCID 2266284613.7%

Reaction Conditions

Temperature112.5 °C

Reaction Steps

In 86 mL of dimethyl sulfoxide was dissolved 4.3 g of N-(5-bromo-3-cyano-2-pyrazinyl)benzamide. After adding 8.3 g of potassium fluoride, the mixture thus obtained was stirred at 110-115° C. for one hour. The reaction mixture was returned to room temperature, a mixture of 100 mL of ethyl acetate and 200 mL of water was added, and the organic layer was separated. The organic layer thus obtained was washed successively with water and saturated aqueous solution of sodium chloride, treated with active charcoal and dried on anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent: toluene:ethyl acetate=5:1] to obtain 0.47 g of N-(3-cyano-5-fluoro-2-pyrazinyl)benzamide as a white-colored solid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800629B2
Source datasetuspto-grants-2004_10
ORD IDord-e816d635e3c2497f86902632a22136ef
Source noteuspto-grants-2004_10