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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| 반응물 | 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine | HCID 22950827 | — |
| 반응물 | (l)-Phenylalanine n-methyl amide trifluoroacetic acid salt | HCID 22950835 | — |
| 반응물 | HCID 178418300 | HCID 178418300 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Dichloromethane methanol | HCID 21226129 | — |
| 생성물 | 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine N-methyl amide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06352976B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-a377d96acc2640bca5fffce9b53ff5dc |
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| 출처 메모 | uspto-grants-2002_03 |
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