参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 碳酸氢铯 | HCID 10796 | — |
| 反应物 | 2-溴苯甲醚 | HCID 11358 | — |
| 反应物 | 水合肼 | HCID 24654 | — |
| 反应物 | 2-双环己基膦-2',6'-二甲氧基联苯 | HCID 11269872 | — |
| 催化剂 | palladium acetate | HCID 167845 | — |
| 溶剂 | (5BETA,17BETA)-17-羟基-17-(甲基-D3)-2'H-雄甾-2-烯并[3,2-C]吡唑-5'(1'H)-酮 | HCID 887 | — |
| 溶剂 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 溶剂 | 乙酸乙酯 | HCID 8857 | — |
| 溶剂 | 1,4-二氧六环 | HCID 31275 | — |
| 产物 | Dicyclohexyl(2',6'-dimethoxy[1,1'-biphenyl]-2-YL)phosphine oxide | HCID 67122844 | 45.4% |
反应步骤
To the mixture of 2-bromoanisole (0.020 ml, 0.16 mmol) and 1,4-dioxane (2 ml), water (0.2 ml), cesium carbonate (0.32 g, 0.97 mmol), sodium 1,3-dioxo-1,3-dihydro-isoindole-2-ylmethyl trifluoroborate (81 mg, 0.32 mmol), palladium(II) acetate (3.6 mg, 0.016 mmol), and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (13 mg, 0.032 mmol) were added, and then the obtained reaction mixture was stirred at 95° C. (an outer temperature) overnight. The reaction mixture was cooled to room temperature, and then hydrazine hydrate (0.039 ml, 0.81 mmol) and methanol (2 ml) were added thereto, followed by heating to reflux for 1 hour. The reaction mixture was cooled to room temperature, and then water and ethyl acetate were added to the reaction mixture, followed by filtration with celite. The organic layer of the filtrate was separated and washed with saline. The solvents were evaporated under reduced pressure from the organic layer, and then the obtained residue was purified with NH-silica gel column chromatography (heptane:ethyl acetate=1:4), thereby obtaining the entitled compound (4.1 mg, 19%) as the mixture with 2′-(dicyclohexyl-phosphinoyl)-2,6-dimethoxy-biphenyl (6.2 mg).
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 专利号 | US08524946B2 |
|---|
| 来源数据集 | uspto-grants-2013_09 |
|---|
| ORD ID | ord-d01713c474f74d42b87c525175407e98 |
|---|
| 来源说明 | uspto-grants-2013_09 |
|---|