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聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 2-Amino-3-(4-chlorocinnamylamino)pyridine
参与物
| 角色 | 名称 | HCID | 投料 |
|---|---|---|---|
| 反应物 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 反应物 | 2,3-二氨基吡啶 | HCID 9956 | — |
| 反应物 | 碳酸钾 | HCID 11430 | — |
| 反应物 | p-Chlorocinnamyl chloride | HCID 53728250 | — |
| 溶剂 | N,N-二甲基甲酰胺 | HCID 6228 | — |
| 产物 | 2-Amino-3-(4-chlorocinnamylamino)pyridine | HCID 54252418 | 42.2% |
反应步骤
7.71 g of p-chlorocinnamyl chloride and 13.5 g of 2,3-diaminopyridine were dissolved in 220 ml of dimethylformamide, and to the solution was added 8.6 g of potassium carbonate, and the mixture was stirred at a room temperature for 50 hours, and after adding 300 ml of water, extracted twice with 200 ml of chloroform. The extract was dried over magnesium sulfate and concentrated under a reduced pressure, and resulting residue was applied to a silica gel column and eluted with chloroform/methanol (100:1 to 50:1), to obtain 4.52 g of the title compound as yellow crystals.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 专利号 | US05245034 |
| 来源数据集 | uspto-grants-1993_09 |
| ORD ID | ord-d4ee0e39c1e94258bf77463d69e44f83 |
| 来源说明 | uspto-grants-1993_09 |