Reacción #75326

Ecuación de reacción

L-alanyl-L-proline ethylamide hydrobromide

p-toluenesulphonyl chloride

→

N-(p-toluenesulphonyl)-L-alanyl-L-proline ethylamide

Rendimiento 33.0%

Disolventes

pyridine

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrothe pyridine was then removed by evaporation
2. 2
   workup.DISSOLUTIONThe oily residue was dissolved in chloroform
3. 3
   Lavadothe solution was washed with water
4. 4
   Secadodried over magnesium sulphate
5. 5
   Otroevaporated to an oil
6. 6
   workup.DISSOLUTIONThis oil was dissolved in water
7. 7
   Otrofreeze-dried

Procedimiento

1.0 g (0.0033 mol) of L-alanyl-L-proline ethylamide hydrobromide was dissolved in 20 ml of dry pyridine and 0.63 g (0.0033 mol) of p-toluenesulphonyl chloride was added. The mixture was stirred at room temperature for 1 hour and the pyridine was then removed by evaporation. The oily residue was dissolved in chloroform and the solution was washed with water, dried over magnesium sulphate and evaporated to an oil. This oil was dissolved in water and freeze-dried to yield 0.40 g (33%) of N-(p-toluenesulphonyl)-L-alanyl-L-proline ethylamide; [α]D20 =-90.7° (c=0.94% in water).

Fuente