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HRID 241生成日期:2026年10月23日

邻氯苯胺 → N-(2-chlorophenyl)-1H-indazol-6-amine

https://huagongshe.com/zh-CN/reaction/241

反应方程式

参与物

角色名称HCID投料
反应物邻氯苯胺HCID 7240—
反应物6-溴吲唑HCID 17842471—
试剂碳酸氢铯HCID 10796—
催化剂1,1'-联萘-2,2'-双二苯膦 (BINAP)HCID 634876—
催化剂醋酸钯HCID 4144353—
溶剂甲苯HCID 1140—
产物N-(2-chlorophenyl)-1H-indazol-6-amineHCID 910618340%

反应条件

温度80 °C

反应步骤

Palladium(II) acetate (0.342 g, 1.52 mmol) and rac-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (1.422 g, 2.28 mmol) were added to a stirred slurry of 2-chloroaniline (1.763 mL, 16.75 mmol), 6-bromo-1H-indazole (3 g, 15.23 mmol) and cesium carbonate (9.92 g, 30.45 mmol) in toluene (50 mL) at 23°C under nitrogen. The resulting slurry was stirred at 80 °C for 2 hours. The reaction was incomplete (both SM left) so the temperature was increased to 100°C and the reaction mixture was stirred for a further 2 hours. Mainly 2 SM detected. problem of solubility of bromoindazole? The reaction was incomplete and further Palladium(II) acetate (30mg), rac-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (200mg) and cesium carbonate (1g) were added as well as dioxane and the slurry was stirred at 110 °C for a further 3 hours. Only SMs detected. No further work on this sample. Perform coupling with reverse coupling partners using Boc 6-aminoindazole. Known to work as used in project.

来源与证据

来源数据集750 AstraZeneca ELN dataset
ORD IDord-870573203c2744a5906bd6a9d998822e
来源说明750 AstraZeneca ELN dataset