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4-溴吡啶 → Ethyl 4-(pyridin-4-ylamino)piperidine-1-carboxylate
参与物
| 角色 | 名称 | HCID | 投料 |
|---|---|---|---|
| 反应物 | 4-溴吡啶 | HCID 14268 | — |
| 反应物 | 4-氨基-1-哌啶甲酸乙酯 | HCID 100867 | — |
| 反应物 | 1,1'-联萘-2,2'-双二苯膦 (BINAP) | HCID 634876 | — |
| 反应物 | 叔丁醇钠 | HCID 23676156 | — |
| 催化剂 | palladium acetate | HCID 167845 | — |
| 溶剂 | 甲苯 | HCID 1140 | — |
| 产物 | Ethyl 4-(pyridin-4-ylamino)piperidine-1-carboxylate | HCID 22293223 | 41.1% |
反应步骤
A solution of ethyl 4-aminopiperidine-1-carboxylate (2.20 g, 12.7 mmol), 4-bromopyridine (3.47 g, 17.8 mmol), sodium t-butoxide (4.54 g, 47.2 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.398 g, 0.639 mmol) and palladium acetate (0.143 g, 0.639 mmol) in toluene (40 mL) was heated at 60° C. overnight. The reaction was cooled and partitioned between ethyl acetate and water. The aqueous layer was washed 3 times with methylene chloride, and the combined organic layers dried over sodium sulfate. The crude product was purified by chromatography (silica gel, 0 to 10% {5% ammonium hydroxide in methanol}in methylene chloride gradient elution), which gave the title compound (1.3 g, 41% yield).
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 专利号 | US07745427B2 |
| 来源数据集 | uspto-grants-2010_06 |
| ORD ID | ord-101a650b45d542b081d56e34c403fdfc |
| 来源说明 | uspto-grants-2010_06 |