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 178418215 | HCID 178418215 | 68.91% |
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 ID | ord-0c726797efaf4f12802e1de309e7f336 |
|---|
| 来源说明 | 750 AstraZeneca ELN dataset |
|---|