Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | HCID 22180767 | HCID 22180767 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 22180765 | HCID 22180765 | 76.9% |
Reaction Steps
A degassed solution of 2,6-dibromopyridine (0.86 g, 3.56 mmol) and 4-(5,5-dimethyl-[1,3,2]dioxaborinan-2-yl)isothiazole (0.35 g, 1.78 mmol) in dry 1,4-dioxane (10 ml) was stirred under an atmosphere of nitrogen, then cesium carbonate (1.20 g, 3.68 mmol) and tetrakis(triphenylphosphine)-palladium(0) (0.10 g, 5 mol %) added. This mixture was heated to reflux for 18 h. After cooling to ambient temperature, solvent was removed in vacuo, the residue dissolved in dichloromethane, 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 on a gradient of methanol (0-5%), gave 2-bromo-6-(isothiazol-4-yl)pyridine (0.33 g) as a white solid: δH (400 MHz, CDCl3) 7.42 (1H, dd, J 7 and 2), 7.60 (2H, m), 9.01 (1H, s), 9.16 (1H, s); m/z (ES+) 240/242 (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-a0a622d06a7a4f0692968fa1b1a1b600 |
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| Source note | uspto-grants-2006_04 |
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