Reacción #95985

Ecuación de reacción

N-methyl-morpholine

chloroformic acid isobutyl ester

agmatine-dichlorohydrate

triethylamine

benzyloxycarbonyl-D-phenylalanyl-L-proline

→

Benzyloxycarbonyl-D-phenylalanyl-L-prolyl-agmatine-chlorohydrate

Disolventes

water

dimethylformamide

dimethylformamide

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONare added
2. 2
   workup.ADDITIONwhen the following solution is poured into it
3. 3
   Temperaturacooled to -15° C
4. 4
   workup.STIRRINGThe reaction mixture is stirred for 2 hours at -15° C., for 1 hour
5. 5
   Temperaturawithout cooling
6. 6
   Otrois evaporated at reduced pressure
7. 7
   workup.DISSOLUTIONThe evaporation residue is dissolved in 100 ml of 0.2 N hydrochloric acid
8. 8
   Extracciónextracted three times with 20 ml of ethyl acetate
9. 9
   Extracciónextracted five times with 20 ml of chloroform
10. 10
    LavadoThe combined chloroform layers are washed twice with 10 ml of water
11. 11
    Otroevaporated at reduced pressure
12. 12
    Filtraciónfiltered
13. 13
    Lavadowashed with diethyl ether
14. 14
    Otroair-dried

Procedimiento

4 g (10 mmoles) of benzyloxycarbonyl-D-phenylalanyl-L-proline (Nikolaides et al.: J.Med.Chem., 11, 74, 1968) are dissolved in 20 ml of dimethylformamide, cooled to -15° C., and at this temperature and constant stirring 1.11 ml (10 mmoles) of N-methyl-morpholine and 1.32 ml (10 mmoles) of chloroformic acid isobutyl ester are added. Stirring is continued for 10 minutes when the following solution is poured into it: 2.05 g (10 mmoles) of agmatine-dichlorohydrate (in formula II A means an H2N--C(NH)-- residue, B a chlorine atom and n=2) are suspended in 15 ml of dimethylformamide, 2 ml of water, then 1.4 ml (10 mmoles) of triethylamine are added, and cooled to -15° C. The reaction mixture is stirred for 2 hours at -15° C., for 1 hour without cooling, then is evaporated at reduced pressure. The evaporation residue is dissolved in 100 ml of 0.2 N hydrochloric acid and extracted three times with 20 ml of ethyl acetate. The pH of the aqueous layer is adjusted with solid sodium hydrogen carbonate to 8.0 to 8.5, and extracted five times with 20 ml of chloroform. The combined chloroform layers are washed twice with 10 ml of water, and evaporated at reduced pressure. The residue is worked up with diethyl ether, filtered, washed with diethyl ether and air-dried. Yield: 4.1 g (75 percent) of the named compound. RF3 0.5 to 0.6.

Fuente