反応 #531775
ord-f36af1f0c6ba4cc79e10cd5b4f7447ae
反応方程式
反応物
試薬
溶媒
反応条件
後処理
- 1workup.STIRRINGThe mixture was stirred for 5 minutes at 0° C.
- 2workup.STIRRINGStirring
- 3workup.WAITat room temperature for 48 hours
- 4温度The reaction mixture was cooled to 0° C.
- 5その他the resulting precipitate was collected
- 6濃縮The filtrate was concentrated in vacuo
- 7workup.DISSOLUTIONThe residue was dissolved in ethyl acetate
- 8抽出the ethyl acetate solution was extracted successively with 1 N sodium bicarbonate, water, 0.75 N citric acid, and water
- 9乾燥The ethyl acetate solution was dried over magnesium sulfate
- 10濃縮concentrated in vacuo
- 11その他The resulting oil was crystallized from ether
- 12その他recrystallized from ethyl acetate
実験手順
To 30 ml. of DMF were added 2.5 gms. (0.005 moles) of Nα -t-butyloxycarbonyl-O-benzyl-L-tyrosyl-D-alanyl-glycine (prepared as in Example 1) and 1.08 gms. (0.005 moles) of the hydrochloride salt of L-phenylalanine, methyl ester. The mixture was stirred at 0° C., and 0.99 ml. (0.005 moles) of dicyclohexylamine was added. The mixture was stirred for 5 minutes at 0° C., and 670 mg. (0.005 mmoles) of HBT and 1.03 gms. (0.005 moles) of DCC were added. Stirring was continued at 0° C. for 2 hours and then at room temperature for 48 hours. The reaction mixture was cooled to 0° C., and the resulting precipitate was collected. The filtrate was concentrated in vacuo. The residue was dissolved in ethyl acetate, and the ethyl acetate solution was extracted successively with 1 N sodium bicarbonate, water, 0.75 N citric acid, and water. The ethyl acetate solution was dried over magnesium sulfate and concentrated in vacuo. The resulting oil was crystallized from ether and recrystallized from ethyl acetate to give 2.7 grams (82%) of the title compound, m.p. 149°-152° C. [α]D25 +22° (C=0.5, MeOH).