Реакция #2467953
ord-33066712eb4d4db8a40659289cebd0b7
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1ДругоеFog 24 hours
- 2Экстракцияthe resulting mixture is extracted three times with chloroform
- 3ПромывкаThe organic layer is washed with 10% hydrochloric acid
- 4Сушкаa saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate
- 5workup.DISTILLATIONAfter the solvent is distilled away under reduced pressure
- 6Другоеthe residue is purified by silica gel column chromatography
Методика
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.