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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276116생성일: 2026년 10월 25일

4-Methylmorpholine → 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine N-methyl amide

https://huagongshe.com/reaction/276116

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanineHCID 22950827—
반응물(l)-Phenylalanine n-methyl amide trifluoroacetic acid saltHCID 22950835—
반응물HCID 178418300HCID 178418300—
용매DichloromethaneHCID 6344—
용매Dichloromethane methanolHCID 21226129—
생성물2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine N-methyl amideHCID 86757825—

반응 단계

Combine (L)-phenylalanine N-methyl amide trifluoroacetic acid salt (0.22 g, 0.75 mmol) and N-methylmorpholine (0.09 mL, 0.83 mmol) in dichloromethane (5 mL). After 15 minutes, add 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine (0.18 g, 0.45 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.086 g, 0.45 mmol) and hydroxybenzotriazole (0.060 g, 0.45 mmol). After 18 hours, partition the reaction mixture between ethyl acetate and an aqueous 5% sulfuric acid solution. Separate the layers, extract the organic layer with a saturated sodium bicarbonate solution and then brine. Dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 4% methanol/dichloromethane to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352976B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-a377d96acc2640bca5fffce9b53ff5dc
출처 메모uspto-grants-2002_03