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HRID 20074生成日期:2026年10月23日

4-溴吡啶 → Ethyl 4-(pyridin-4-ylamino)piperidine-1-carboxylate

https://huagongshe.com/zh-CN/reaction/20074

反应方程式

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 acetateHCID 167845—
溶剂甲苯HCID 1140—
产物Ethyl 4-(pyridin-4-ylamino)piperidine-1-carboxylateHCID 2229322341.1%

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

DOI10.6084/m9.figshare.5104873.v1
专利号US07745427B2
来源数据集uspto-grants-2010_06
ORD IDord-101a650b45d542b081d56e34c403fdfc
来源说明uspto-grants-2010_06