HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796076Generated: November 3, 2026
2,6-Dibromopyridine → HCID 22180772, compound
https://huagongshe.com/reaction/1796076
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | 1h-1,2,4-Triazole sodium salt | HCID 45489822 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22180772 | HCID 22180772 | 45% |
Reaction Steps
A stirred solution of 2,6-dibromopyridine (2.0 g, 8.3 mmol) and 1,2,4-triazole sodium salt (1.0 g, 9.9 mmol) in dimethylsulfoxide (10 ml) was heated at 60° C. for 5 h. After cooling to ambient temperature the reaction was diluted with water and extracted into dichloromethane. Combined organic extracts were washed with water and saturated brine then dried over magnesium sulfate, filtered and evaporated in vacuo to give a solid. Purification by chromatography on silica gel eluting with dichloromethane, then dichloromethane containing 5% methanol, gave 2-bromo-6-(1H-[1,2,4]triazol-1-yl)pyridine (0.84 g) as a white solid: δH (400 MHz, CDCl3) 7.49 (1H, d, J 8), 7.74 (1H, dd, J 8 and 8), 7.87 (1H, d, J 8), 8.09 (1H, s), 9.15 (1H, s); m/z (ES+) 224/226 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030128B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-e50726fde56844959515246589ac0676 |
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| Source note | uspto-grants-2006_04 |
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