参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 结晶磺胺 | HCID 5333 | — |
| 反应物 | 3-(2-Chloropyridin-4-yl)oxy-2,6-dimethyl-pyridine | HCID 44598200 | — |
| 试剂 | 碳酸氢铯 | HCID 10796 | — |
| 催化剂 | 4,5-双二苯基膦-9,9-二甲基氧杂蒽 | HCID 636044 | — |
| 催化剂 | 醋酸钯 | HCID 4144353 | — |
| 溶剂 | N,N-二甲基乙酰胺 | HCID 31374 | — |
| 产物 | 4-((4-[(2,6-DIMETHYLPYRIDIN-3-YL)OXY]PYRIDIN-2-YL)AMINO)BENZENESULFONAMIDE | HCID 25192277 | 76.03% |
反应步骤
XANTPHOS (2.466 g, 4.26 mmol) was added to 3-(2-chloropyridin-4-yloxy)-2,6-dimethylpyridine (10g, 42.61 mmol), Sulfanilamide (9.54 g, 55.39 mmol) and CESIUM CARBONATE (20.83 g, 63.92 mmol) in DMA (200 ml) at 20ºC. Nitrogen was bubbled through the reaction mixture for 1 hour then PALLADIUM(II) ACETATE (0.670 g, 2.98 mmol) added. The suspension was stirred at 130 °C for 3 hours. The reaction mixture was filtered then evaporated to dryness. The residue was triturated with water (150 mL) and filtered to give crude product as a cream solid - 90% pure. The crude solid was triturated with hot acetonitrile (300 mL) and filtered to afford crude product as a cream solid - 98% by LCMS. This was combined with the product from EN02084-31 and dissolved in boiling acetonitrile (approx 1 L). The solution was concentrated to 500 mL and cooled to ice bath temperature with stirring. A precipitate formed which and the suspension was stirred at room temperature overnight. The solid was filtered to afford 4-(4-(2,6-dimethylpyridin-3-yloxy)pyridin-2-ylamino)benzenesulfonamide (12.00 g, 76 %) as a cream solid.
来源与证据
| 来源数据集 | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-c34e3f2a76e4462999414a169b276944 |
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| 来源说明 | 750 AstraZeneca ELN dataset |
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