Reacción #2467953
ord-33066712eb4d4db8a40659289cebd0b7
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroFog 24 hours
- 2Extracciónthe resulting mixture is extracted three times with chloroform
- 3LavadoThe organic layer is washed with 10% hydrochloric acid
- 4Secadoa saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate
- 5workup.DISTILLATIONAfter the solvent is distilled away under reduced pressure
- 6Otrothe 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.