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HRID 4950生成日期:2026年10月23日

醋酸 → N-(1-azabicyclo[2.2.2]oct-3 yl)-N'-(3-chlorphenyl)-1,2-diaminoethane

https://huagongshe.com/zh-CN/reaction/4950

反应方程式

参与物

角色名称HCID投料
反应物醋酸HCID 176—
反应物1-Azabicyclo(2.2.2)octan-3-one, hydrochloride (1:1)HCID 102019—
反应物氰基硼氢化钠HCID 5003444—
反应物N1-(3-chlorophenyl)ethane-1,2-diamineHCID 11008376—
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—
产物N-(1-azabicyclo[2.2.2]oct-3 yl)-N'-(3-chlorphenyl)-1,2-diaminoethaneHCID 104929773.7%

反应步骤

To a stirred solution of N-(3-chlorophenyl)-1,2-diaminoethane (1 g; 0,00586 moles) in 25 ml of anhydrous methanol kept under nitrogen atmosphere, 3-quinuclidinone hydrochloride (1.01 g, 0.0062? moles) is added. The pH is adjusted to pH 6 by addition of glacial acetic acid. Sodium cyanoborohydride (0.74 g; 0.0117 moles) is added in two portions. The reaction mixture is refluxed for 10 hours, cooled and then filtered. After evaporation to dryness the residue is taken up with water, basified with 20% sodium hydroxide solution and extracted three times with ethyl acetate. The organic layer is washed with brine, dried over anhydrous sodium sulfate and, after filtration, evaporated to dryness. The residue is purified by silica gel flash-chromatography (methylene chloride--methanol--30% ammonium hydroxide, 150:50:5 as eluant) to give the desired product as a clear oil (0.06 g).

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US05242929
来源数据集uspto-grants-1993_09
ORD IDord-6155d4e4a76d41d69a88452893850b2d
来源说明uspto-grants-1993_09