Reaktion #342763

Reaktionsgleichung

L-glutamic acid

L-phenylalanine benzyl ester toluenesulfonic acid

N-ethylmorpholine

dicyclohexylcarbodiimide

→

L-glutamyl-L-phenylalanine benzyl ester

Lösungsmittel

dimethylformamide

dichloromethane

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGThe reaction mixture was stirred in an ice water bath for 1 hour
2. 2
   Sonstigeat room temperature
3. 3
   Sonstigeovernight
4. 4
   SonstigeDicyclohexylurea was removed by filtration
5. 5
   Waschenthe product was washed in ethyl acetate
6. 6
   SonstigeSolvents of the combined filtrates were removed under reduced pressure with a rotary evaporator at 40° C
7. 7
   workup.ADDITIONEthyl acetate (25 ml) was added to the residue
8. 8
   Waschenthe organic solution was washed until neutral
9. 9
   TrocknenThe organic phase was dried over anhydrous MgSO4
10. 10
    Filtrationfiltered
11. 11
    Sonstigethe solvent was removed with a rotary evaporator
12. 12
    SonstigeThe material was crystalized from isopropanol and ether, yield: 1.01 g of white needles, m.p. 103°-104.5° C

Vorschrift

A solution of 0.52 g of pyro-L-glutamic acid, 1.72 g of L-phenylalanine benzyl ester toluenesulfonic acid and 0.55 mg of N-ethylmorpholine in 5 ml of dimethylformamide (DMF) and 20 ml of dichloromethane was cooled in an ice bath with stirring. A solution of 0.826 g of dicyclohexylcarbodiimide in 2 ml dichloromethane was added to the above reaction mixture. The reaction mixture was stirred in an ice water bath for 1 hour and then at room temperature overnight. Dicyclohexylurea was removed by filtration and the product was washed in ethyl acetate. Solvents of the combined filtrates were removed under reduced pressure with a rotary evaporator at 40° C. Ethyl acetate (25 ml) was added to the residue and the organic solution was washed until neutral. The organic phase was dried over anhydrous MgSO4, filtered and then the solvent was removed with a rotary evaporator. The material was crystalized from isopropanol and ether, yield: 1.01 g of white needles, m.p. 103°-104.5° C. The material was homogeneous on all TLC and electrophoresis systems.

Quelle