Reacción #1155265

ord-184297fd148c4f2d9f87bb8c352a0d9b

Ecuación de reacción

CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
O.On1nnc2ccccc21
1-hydroxybenzo-triazole hydrate
COC(=O)[C@H](C)N.Cl
(L)-alanine methyl ester hydrochloride
CSCC[C@@H](NC(=O)OC(C)(C)C)C(=O)O
Boc-(D)-methionine
CN1CCOCC1
N-Methylmorpholine
COC(=O)[C@H](C)NC(=O)[C@@H](CCSC)NC(=O)OC(C)(C)C
Boc-(D)-Met-(L)-Ala-OMe
Rendimiento 84.8%

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturamaintaining the temperature of the mixture at 0-5° C
  2. 2
    Temperaturamaintaining the temperature of the mixture at 0-5° C
  3. 3
    LavadoThe reaction mixture is washed successively with water (2×100 ml), 10% aqueous citric acid solution (100 ml), saturated aqueous sodium bicarbonate solution (100 ml), water (100 ml)
  4. 4
    Otroevaporated to dryness at 40° C. under reduced pressure

Procedimiento

Boc-(D)-methionine (50.0 g) is dissolved in dichloromethane (200 ml) and 1-hydroxybenzo-triazole hydrate (29.7 g) and (L)-alanine methyl ester hydrochloride (31.0 g) is added. The mixture is cooled to 0° C. and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (43.0 g) is added in portions, maintaining the temperature of the mixture at 0-5° C. N-Methylmorpholine (42.2 g) is then added over 30 minutes, maintaining the temperature of the mixture at 0-5° C. The mixture is then stirred at 0° C. for 5 hours. The reaction mixture is washed successively with water (2×100 ml), 10% aqueous citric acid solution (100 ml), saturated aqueous sodium bicarbonate solution (100 ml), water (100 ml) and evaporated to dryness at 40° C. under reduced pressure to give Boc-(D)-Met-(L)-Ala-OMe (67.0 g estimated to contain 0.17 mol) as an oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06248903B1uspto-grants-2001_06