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HRID 6生成日期:2026年10月23日

结晶磺胺 → 4-((4-[(2,6-DIMETHYLPYRIDIN-3-YL)OXY]PYRIDIN-2-YL)AMINO)BENZENESULFONAMIDE

https://huagongshe.com/zh-CN/reaction/6

反应方程式

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-pyridineHCID 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)BENZENESULFONAMIDEHCID 2519227776.03%

反应条件

温度130 °C

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
ORD IDord-c34e3f2a76e4462999414a169b276944
来源说明750 AstraZeneca ELN dataset