HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879577Generated: October 30, 2026
Potassium Acetate → 3-Methyl-[1,2,3]triazolo[1,5-a]pyridin-5-ylboronic acid
https://huagongshe.com/reaction/879577
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reactant | 5-Bromo-3-methyl-[1,2,3]triazolo[1,5-a]pyridine | HCID 82660536 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Methyl-[1,2,3]triazolo[1,5-a]pyridin-5-ylboronic acid | HCID 86700396 | — |
Reaction Steps
To a vial flushed with argon was added 5-bromo-3-methyl-[1,2,3]triazolo[1,5-a]pyridine (424 mg, 2 mmol), PdCl2(dppf)-DCM (327 mg, 0.4 mmol), bis(pinacolato)diboron (660 mg, 2.6 mmol), and KOAc (589 mg, 6 mmol). Anhydrous dioxane (10 mL) was added, and the mixture was heated to 100° C. for 3 hours. After cooling to room temperature, the mixture was filtered over a plug of Celite, and concentrated to provide the crude product, which was used directly without further purification. LCMS-ESI+: calc'd for C7H9BN3O2: 178.1 (M+H+); Found: 178.04 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987250B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-4473cd2a509347d4862219db5590f92e |
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| Source note | uspto-grants-2015_03 |
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