反应 #1994224
ord-63c7f83afefd4282930dd4f4fde5c3c6
反应方程式
溶剂
反应条件
后处理
- 1温度The solution was cooled in an ice-water bath for 5 min
- 2其他the bath was removed
- 3workup.ADDITIONTo the solution DCC was added (778 mg, 3.73 mmol, 2.4 equiv.)
- 4workup.STIRRINGto stir at room temperature under argon
- 5其他reaction
- 6过滤The reaction mixture was filtered
- 7浓缩the filtrate was concentrated to dryness on a rotary-evaporator
- 8其他The crude product was then purified by silica gel chromatography
- 9workup.DISSOLUTIONThe crude product was dissolved in a mixed solvent of hexane-ethyl acetate (6 mL, 4:1 v/v)
- 10洗涤The column was eluted with hexane-ethyl acetate (4:1 v/v)
- 11其他evaporated by rotary-evaporation
- 12其他dried under vacuum overnight
实验过程
In a 50 mL round bottom flask, rotigotine (500 mg, 1.56 mmol, 1 equiv.), 3-azidopropionic acid (447 mg, 3.73 mmol, 2.4 equiv.—in 5 mL DCM), and pyridine (302 μL, 3.73 mmol, 2.4 equiv.) were dissolved in 50 mL anhydrous DCM and allowed to stir under argon. The solution was cooled in an ice-water bath for 5 min, and the bath was removed. To the solution DCC was added (778 mg, 3.73 mmol, 2.4 equiv.). The solution was allowed to stir at room temperature under argon. Following overnight reaction, reverse phase HPLC analysis of the reaction mixture showed complete conversion of free rotigotine to the ester form. The reaction mixture was filtered and the filtrate was concentrated to dryness on a rotary-evaporator. The crude product was then purified by silica gel chromatography. The crude product was dissolved in a mixed solvent of hexane-ethyl acetate (6 mL, 4:1 v/v) and then loaded onto a 300 mL silica gel column (30 mm id). The column was eluted with hexane-ethyl acetate (4:1 v/v). The fractions (10 mL each) were analyzed by TLC and reversed phase HPLC. The product fractions were pooled, evaporated by rotary-evaporation, and then dried under vacuum overnight. Yield: 292 mg.