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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 904961생성일: 2026년 10월 26일

Ethylmorpholine → Z-Val-Tyr(But)-OBut

https://huagongshe.com/reaction/904961

반응식

참여 물질

역할이름HCID투입량
반응물EthylmorpholineHCID 7525—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물N-Carbobenzoxy-L-valineHCID 726987—
반응물Tert-butyl (2S)-2-amino-3-[4-(tert-butoxy)phenyl]propanoateHCID 7350495—
용매DimethylformamideHCID 6228—
생성물Z-Val-Tyr(But)-OButHCID 131713283—

반응 조건

온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04420424
출처 데이터셋uspto-grants-1983_12
ORD IDord-05bbf4852bd54c4f8f5d82550b654830
출처 메모uspto-grants-1983_12