HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440892Generated: October 25, 2026
Water → 2-Amino-3-cyano-5-[3,5-di(trifluoromethyl)phenyl]pyrazine
https://huagongshe.com/reaction/440892
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Bis-trifluoromethylphenylboronic acid | HCID 156265 | — |
| Reactant | 3-Amino-6-bromopyrazine-2-carbonitrile | HCID 11052611 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Amino-3-cyano-5-[3,5-di(trifluoromethyl)phenyl]pyrazine | HCID 15335268 | — |
Reaction Steps
A stirred solution of 1.6 grams (0.008 mole) of 2-amino-3-cyano-5-bromopyrazine [prepared by the method of Taylor and Ray--JOC, 52, 3997 (1987)], 3.2 grams (0.012 mole) of 3,5-di(trifluoromethyl)phenylboronic acid commercially available or prepared by the method of Thompson and Gaudino--JOC, 49, 5237 (1984)], 4.3 grams (0.031 mole) of potassium carbonate and 0.3 gram of tetrakis(triphenylphosphine)palladium(0) in 150 mL of toluene is heated at 90° C. for about 20 hours. After this time, the reaction mixture is stirred with 100 mL of water, and the organic layer is separated. The organic layer is concentrated under reduced pressure to a residue. The residue is subjected to column chromatography on silica gel. The product-containing fractions are combined and concentrated under reduced pressure, yielding 2-amino-3-cyano-5-[3,5-di(trifluoromethyl)phenyl]pyrazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05521190 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-0daa9f0493404b04bb0ee48ace48d093 |
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| Source note | uspto-grants-1996_05 |
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