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HRID 31080生成日期:2026年10月23日

聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → (E)-2-(吡啶-3-亚甲基)奎宁环素-3-酮

https://huagongshe.com/zh-CN/reaction/31080

反应方程式

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3-吡啶甲醛HCID 10371—
反应物氢氧化钾HCID 14797—
反应物1-Azabicyclo(2.2.2)octan-3-one, hydrochloride (1:1)HCID 102019—
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(E)-2-(吡啶-3-亚甲基)奎宁环素-3-酮HCID 61182276.2%

反应步骤

Potassium hydroxide (56 g, 0.54 mole) was dissolved in methanol (420 mL). 3-Quinuclidinone hydrochloride (75 g, 0.49 mole) was added and the mixture was stirred for 30 min at ambient temperature. 3-Pyridinecarboxaldehyde (58 g, 0.54 mole) was added and the mixture stirred for 16 h at ambient temperature. The reaction mixture became yellow during this period, with solids caking on the walls of the flask. The solids were scraped from the walls and the chunks broken up. With rapid stirring, water (390 mL) was added. When the solids dissolved, the mixture was cooled at 4° C. overnight. The crystals were collected by filtration, washed with water, and air dried to obtain 80 g of yellow solid. A second crop (8 g) was obtained by concentration of the filtrate to ˜10% of its former volume and cooling at 4° C. overnight. Both crops were sufficiently pure for further transformation (88 g, 82%).

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US07425561B2
来源数据集uspto-grants-2008_09
ORD IDord-e9df5fb87eb04db0b64bbf87f9d32055
来源说明uspto-grants-2008_09