Reacción #2467953

ord-33066712eb4d4db8a40659289cebd0b7

Ecuación de reacción

CC(=O)NC(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)O
N-[2-(Acetylamino)propionyl]phenylalanine
CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
On1nnc2ccccc21
1-hydroxybenzotriazole
C1CCNCC1
piperidine
CC(=O)NC(C)C(=O)NC(Cc1ccccc1)C(=O)N1CCCCC1
1-{2-[N-(2-(acetylamino)propionyl)amino]-3-phenylpropionyl}piperidine

Condiciones de reacción

Temperatura
50°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroFog 24 hours
  2. 2
    Extracciónthe resulting mixture is extracted three times with chloroform
  3. 3
    LavadoThe organic layer is washed with 10% hydrochloric acid
  4. 4
    Secadoa saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONAfter the solvent is distilled away under reduced pressure
  6. 6
    Otrothe residue is purified by silica gel column chromatography

Procedimiento

N-[2-(Acetylamino)propionyl]phenylalanine obtained in Experimental Example 21 (10 mg, 0.036 mmol) is suspended in N,N-dimethylformamide (5 ml), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (14 mg, 0.073 mmol), 1-hydroxybenzotriazole (15 mg, 0.11 mmol) and piperidine (40 μl, 0.40 mmol) are added to the suspension at room temperature, followed by stirring at 50° C. Fog 24 hours. To the reaction mixture is added water, and the resulting mixture is extracted three times with chloroform. The organic layer is washed with 10% hydrochloric acid and a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. After the solvent is distilled away under reduced pressure, the residue is purified by silica gel column chromatography to obtain 1-{2-[N-(2-(acetylamino)propionyl)amino]-3-phenylpropionyl}piperidine.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08257943B2uspto-grants-2012_09