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HRID 2373071作成日:2026年10月26日

4-Methylmorpholine → Z-Gly-Leu-PheCH2F

https://huagongshe.com/reaction/2373071

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物BenzyloxycarbonylglycineHCID 14349—
反応物Sodium HydroxideHCID 14798—
反応物Z-Gly-Leu-OHHCID 96816—
反応物PheCH2F hydrochlorideHCID 131717227—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物Z-Gly-Leu-PheCH2FHCID 13171722954%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05101068
出典データセットuspto-grants-1992_03
ORD IDord-1a2cdad7a44c445db5cfed2e12ca1dee
出典メモuspto-grants-1992_03