Reaction #2467953
ord-33066712eb4d4db8a40659289cebd0b7
Reaction equation
Reactants
Reagents
Solvents
Conditions
Workup
- 1OtherFog 24 hours
- 2Extractionthe resulting mixture is extracted three times with chloroform
- 3WashThe organic layer is washed with 10% hydrochloric acid
- 4Dryinga saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate
- 5workup.DISTILLATIONAfter the solvent is distilled away under reduced pressure
- 6Otherthe residue is purified by silica gel column chromatography
Procedure
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.