돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2373071생성일: 2026년 10월 26일

4-Methylmorpholine → Z-Gly-Leu-PheCH2F

https://huagongshe.com/reaction/2373071

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물BenzyloxycarbonylglycineHCID 14349—
반응물Sodium HydroxideHCID 14798—
반응물Z-Gly-Leu-OHHCID 96816—
반응물PheCH2F hydrochlorideHCID 131717227—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물Z-Gly-Leu-PheCH2FHCID 13171722954%

반응 단계

Z-Gly-LeuOH was made by mixed anhydride coupling of Z-GlyOH and LeuOBzl tosylate, followed by NaOH hydrolysis of the benzyl ester. To a solution of Z-Gly-LeuOH (0.223 g, 0.69 mmol) in THF (4 mL) at -20° C. was added NMM (76 uL, 0.69 mmol), followed by IBCF (90 uL, 0.69 mmol). After 10 minutes, a precooled solution of PheCH2F hydrochloride (0.15 g, 0.69 mmol) in DMF (1 mL) was added, followed by a second equivalent (76 uL, 0.69 mmol) of NMM. After 30 minutes of stirring, the mixture was quenched with 1M HCl (5 mL), extracted with ethyl acetate (20 mL), washed with saturated aqueous NaHCO3 (6 mL), brine (5 mL), dried over MgSO4, filtered, and evaporated to dryness. The residue was crystallized from ether/hexane to give 0.18 g (54%) of Z-Gly-Leu-PheCH2F.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05101068
출처 데이터셋uspto-grants-1992_03
ORD IDord-1a2cdad7a44c445db5cfed2e12ca1dee
출처 메모uspto-grants-1992_03