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HRID 904961作成日:2026年10月27日

Ethylmorpholine → Z-Val-Tyr(But)-OBut

https://huagongshe.com/reaction/904961

反応式

関与物質

役割名称HCID仕込み量
反応物EthylmorpholineHCID 7525—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物N-Carbobenzoxy-L-valineHCID 726987—
反応物Tert-butyl (2S)-2-amino-3-[4-(tert-butoxy)phenyl]propanoateHCID 7350495—
溶媒DimethylformamideHCID 6228—
生成物Z-Val-Tyr(But)-OButHCID 131713283—

反応条件

温度0 °C

反応手順

13 ml (approx. 0.1 mole) of N-ethylmorpholine and 22 g (107 mmoles) of dicyclohexylcarbodiimide are added at 0° C. to a solution in 150 ml of dimethylformamide of 33 g (0.1 mole) of H-Tyr(But)-OBut, 25.1 g (0.1 mole) of Z-Val-OH and 13.5 g of 1-hydroxybenzotriazole. The mixture is stirred for one hour at 0° C. and allowed to stand overnight at room temperature. The precipitate is filtered off and the filtrate is concentrated. The residue is partitioned between 300 ml of ethyl acetate and 300 ml of water. The ethyl acetate phase is extracted by shaking successively with 100 ml of saturated NaHCO3 solution, 100 ml of KHSO4 /K2SO4 solution, 100 ml of saturated NaHCO3 solution and 100 ml of water. After drying over Na2SO4 the solution is concentrated. The residue is triturated with petroleum ether, cooled and filtered off. Yield 31.2 g (60%), melting point 82°-83°, [α]D21 =-20.9° (c=1, methanol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04420424
出典データセットuspto-grants-1983_12
ORD IDord-05bbf4852bd54c4f8f5d82550b654830
出典メモuspto-grants-1983_12