反应 #43736

反应方程式

sodium hydroxide

water

tin(II) chloride

N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-nitro-1-benzofuran-2-carboxamide

→

title compound

N-[(3R)-1-Azabicyclo[2.2.2]oct-3-yl]-5-amino-1-benzofuran-2-carboxamide

溶剂

DMF

反应条件

后处理

1. 1
   萃取The aqueous phase is extracted six times with ethyl acetate
2. 2
   干燥The combined organic phases are dried over magnesium sulfate
3. 3
   其他the solvent is removed under reduced pressure
4. 4
   其他a rotary evaporator
5. 5
   workup.STIRRINGshaken together with acidic ion exchange resin (Dowex WX2-200) for about 20 min
6. 6
   洗涤The loaded ion exchanger is washed three times with in each ase 30 ml of methanol
7. 7
   洗涤The product is eluted
8. 8
   其他The solvent is removed under reduced pressure
9. 9
   其他a rotary evaporator

实验过程

2.0 ml (4 mmol) of a 2 M tin(II) chloride solution in DMF are added to N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-nitro-1-benzofuran-2-carboxamide (100 mg, 0.32 mmol). The mixture is stirred overnight. The reaction mixture is poured into water and made basic using 1N aqueous sodium hydroxide solution. The aqueous phase is extracted six times 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 shaken together with acidic ion exchange resin (Dowex WX2-200) for about 20 min. The loaded ion exchanger is washed three times with in each ase 30 ml of methanol, then with water/methanol 8:2, again with methanol, with dichloromethane and finally again with methanol. The product is eluted using methanol/triethylamine 95:5. The solvent is removed under reduced pressure using a rotary evaporator. 52 mg (58% of theory) of the title compound are isolated.

来源