反应 #95076

反应方程式

2-(N,N-diethylamino)ethanol

N-decyl-3-(3-[4-carboxy-2-oxo-pyrrolidino]phenyl)propenamide

carbonyldiimidazole

2-(N,N-diethylamino)ethanol

→

N-Decyl-3-(3-[4-(2-[N,N-diethylamino]ethoxycarbonyl)-2-oxo-pyrrolidino]phenyl)propenamide

溶剂

tetrahydrofuran

反应条件

后处理

1. 1
   温度The mixture was heated
2. 2
   温度under reflux for 10 minutes
3. 3
   温度The mixture was again heated
4. 4
   温度under reflux for 10 minutes
5. 5
   温度The mixture was heated
6. 6
   温度under reflux for 15 minutes
7. 7
   其他The solvent was removed by evaporation in vacuo
8. 8
   workup.DISSOLUTIONthe residue was dissolved in 75 ml
9. 9
   洗涤The ethyl acetate solution was washed successively with water, 1 N sodium hydroxide, water and saturated sodium chloride solution
10. 10
    干燥The ethyl acetate solution was then dried
11. 11
    其他the ethyl acetate was removed by evaporation in vacuo
12. 12
    其他The residue (960 mg.) was recrystallized from isopropyl ether giving 570 mg

实验过程

To a stirred solution of 829 mg. of N-decyl-3-(3-[4-carboxy-2-oxo-pyrrolidino]phenyl)propenamide in 25 ml. of tetrahydrofuran was added 357 mg. of carbonyldiimidazole. The mixture was heated under reflux for 10 minutes, and then 258 mg. of 2-(N,N-diethylamino)ethanol was added. The mixture was again heated under reflux for 10 minutes, and then an additional 258 mg. of 2-(N,N-diethylamino)ethanol was added. The mixture was heated under reflux for 15 minutes and then it was cooled to room temperature. The solvent was removed by evaporation in vacuo, and the residue was dissolved in 75 ml. of ethyl acetate. The ethyl acetate solution was washed successively with water, 1 N sodium hydroxide, water and saturated sodium chloride solution. The ethyl acetate solution was then dried using sodium sulfate, and the ethyl acetate was removed by evaporation in vacuo. The residue (960 mg.) was recrystallized from isopropyl ether giving 570 mg. of the title compound, m.p. 78°-80° C.

来源