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HRID 15464生成日期:2026年10月23日

N,N-二异丙基乙胺 → N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5,7-difluoro-1-benzofuran-2-carboxamide

https://huagongshe.com/zh-CN/reaction/15464

反应方程式

参与物

角色名称HCID投料
反应物N,N-二异丙基乙胺HCID 81531—
反应物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反应物R-3-氨基奎宁环二盐酸盐HCID 12494972—
反应物5,7-二氟苯并呋喃-2-羧酸HCID 59341426—
溶剂N,N-二甲基甲酰胺HCID 6228—
产物N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5,7-difluoro-1-benzofuran-2-carboxamideHCID 59341435—

反应步骤

55 mg (0.28 mmol) of 5,7-difluoro-1-benzofuran-2-carboxylic acid, 50 mg (0.25 mmol) of (R)-3-aminoquinuclidine dihydrochloride, 114.6 mg (0.3 mmol) of HATU, 117 mg (0.9 mmol) of N,N-diisopropylethylamine and 2.0 ml of DMF are reacted according to the general procedure (variant B). DMF is removed under reduced pressure and the crude product is dissolved in 1N aqueous sodium hydroxide solution. The aqueous phase is extracted with ethyl acetate. The combined organic phases are dried over magnesium sulfate and the solvent is removed under reduced pressure using a rotary evaporator. The crude product is taken up in methanol and, together with acidic ion exchange resin (Dowex WX2-200), shaken for about 20 min. The loaded ion exchanger is washed three times with in each case 30 ml of methanol, then with water, again with methanol, with dichloromethane and finally again with methanol. The product is eluted with methanol/triethylamine 95:5. The solvent is removed under reduced pressure using a rotary evaporator. 40 mg (52% of theory) of the title compound are isolated.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US07732477B2
来源数据集uspto-grants-2010_06
ORD IDord-bb2b1acbb9aa4d18911994645d145dcd
来源说明uspto-grants-2010_06