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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | N-(5-bromo-3-cyano-2-pyrazinyl)benzamide | HCID 22662825 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-(3-cyano-5-fluoro-2-pyrazinyl)benzamide | HCID 22662846 | 13.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06800629B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-e816d635e3c2497f86902632a22136ef |
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| Source note | uspto-grants-2004_10 |
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