HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178418268, compound → 6,8-Dibromo-2-furan-2-yl-[1,2,4]triazolo[1,5-a]pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178418268 | HCID 178418268 | — |
| Reactant | HCID 178512066 | HCID 178512066 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6,8-Dibromo-2-furan-2-yl-[1,2,4]triazolo[1,5-a]pyrazine | HCID 86007546 | 40% |
Reaction Steps
A mixture of N-(3,5-dibromo-pyrazin-2-yl)-furan-2-carboxamidine (47 g, 0.14 mol), lead tetraacetate (95% purity, 160 g, 0.34 mol), and toluene (940 ml) was refluxed for 2 hours. The reaction was allowed to cool to room temperature and concentrated in vacuo. The resulting residue was purified by flash column chromatography on silica (hexanes:EtOAc (5:1 to 3:1)) as eluent to afford 6,8-dibromo-2-furan-2-yl-[1,2,4]triazolo[1,5-a]pyrazine as a yellow solid (19.2 g, 40% yield). 1H NMR (300 MHz, CDCl3) δ 6.60 (dd, 1H), 7.33 (d, 1H), 7.62 (d, 1H), 8.63 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07674791B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-0eaaf5f2ec174970afb48501280d32bc |
| Source note | uspto-grants-2010_03 |