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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276117생성일: 2026년 10월 26일

Carbon Tetrachloride → 2-mercapto-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine-N-methyl amide

https://huagongshe.com/reaction/276117

반응식

참여 물질

역할이름HCID투입량
반응물Carbon TetrachlorideHCID 5943—
반응물AnisoleHCID 7519—
반응물2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine N-methyl amideHCID 86757825—
촉매Mercuric acetateHCID 15337—
용매DichloromethaneHCID 6344—
생성물2-mercapto-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine-N-methyl amideHCID 5987874480.5%

반응 단계

Combine 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine N-methyl amide (0.26 g, 0.45 mmol), mercury (II) acetate (0.156 g, 0.49 mmol), and anisole (0.49 mL, 4.5 mmol) in dichloromethane (10 mL). Cool in an ice bath and degas by repeatedly applying vacuum and filling the vessel with nitrogen. Add trifluoroacetic acid (2 mL). After 3 hours, filter and evaporate in vacuo to give a residue. Repeatedly, combine the residue and carbon tetrachloride and evaporate in vacuo to give a residue. Triturate the residue with hexane to give the title compound as a solid (165 mg, 80.4%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352976B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-27473199c8ff43b1ac82c772cd020e0b
출처 메모uspto-grants-2002_03