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HRID 550生成日期:2026年10月23日

2-溴苯甲醚 → HCID 178418215,化合物

https://huagongshe.com/zh-CN/reaction/550

反应方程式

参与物

角色名称HCID投料
反应物2-溴苯甲醚HCID 11358—
反应物(1S,4S)-2-BOC-2,5-二氮双环[2.2.1]庚烷HCID 11521263—
试剂叔丁醇钠HCID 23676156—
催化剂1,1'-联萘-2,2'-双二苯膦 (BINAP)HCID 634876—
催化剂三(二亚苄基丙酮)二钯HCID 9811564—
溶剂甲苯HCID 1140—
产物HCID 178418215HCID 17841821568.91%

反应条件

温度105 °C

反应步骤

TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (0.046 g, 0.05 mmol) and rac-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.063 g, 0.10 mmol) were mixed together and evacuated and purged with nitrogen 3 times. toluene (24.91 ml) was added and the resulting mixture heated to 50°C for 10 minutes. In a second reaction vessel was mixed sodium tert-butoxide (0.387 g, 4.03 mmol), (1S,4S)-tert-butyl 2,5-diazabicyclo[2.2.1]heptane-2-carboxylate (0.500 g, 2.52 mmol), 1-bromo-2-methoxybenzene (0.314 ml, 2.52 mmol) and toluene (24.91 ml). The mixture was evacuated and purged with nitrogen 3 times. The solution of catalyst was added to the reaction mixture and the resulting mixture was heated at 105 °C for 16 hours. The reaction mixture was cooled to RT and filtered through celite and evaporated. The crude product was purified by flash silica chromatography, elution gradient 100% DCM. Pure fractions were evaporated to dryness to afford (1S,4S)-tert-butyl 5-(2-methoxyphenyl)-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate (0.529 g, 68.9 %) as a yellow gum.

来源与证据

来源数据集750 AstraZeneca ELN dataset
ORD IDord-0c726797efaf4f12802e1de309e7f336
来源说明750 AstraZeneca ELN dataset