Reacción #343674

ord-36c498b4fc154cc8999156e4508253f2

Ecuación de reacción

CCOC(=O)CN.Cl
H-Gly-OEt.HCl
CC(C)[C@H](NC(=O)OC(C)(C)C)C(=O)O
Boc-Val-OH
On1nnc2ccccc21
HOBT
CCN=C=NCCCN(C)C.Cl
WSC.HCl
CCOC(=O)CNC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C
Boc-Val-Gly-OEt
Rendimiento 85.3%

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Temperatura
-5°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe reaction mixture was concentrated under reduced pressure
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in ethyl acetate
  3. 3
    Lavadosuccessively washed three times with 1N hydrochloric acid
  4. 4
    Secadoonce with saturated aqueous sodium chloride, three times with 5% aqueous sodium hydrogen carbonate, three times with saturated aqueous sodium chloride, and dried over anhydrous sodium sulfate
  5. 5
    Concentraciónfollowed by concentration under reduced pressure
  6. 6
    OtroThe residue was recrystallized from ethyl acetate-n-hexane

Procedimiento

To a solution of 3.21 g of the H-Gly-OEt.HCl dissolved in 10 ml of DMF, under cooling at -5° C., 5.00 g of Boc-Val-OH, 3.10 g of HOBT and 4.79 g of WSC.HCl were added, and the mixture was stirred at -5° C. for one hour and at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate, successively washed three times with 1N hydrochloric acid, once with saturated aqueous sodium chloride, three times with 5% aqueous sodium hydrogen carbonate, three times with saturated aqueous sodium chloride, and dried over anhydrous sodium sulfate, followed by concentration under reduced pressure. The residue was recrystallized from ethyl acetate-n-hexane to give 5.93 g (yield: 85.2%) of Boc-Val-Gly-OEt melting at 91.5° to 93° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04703106uspto-grants-1987_10