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HRID 276117作成日:2026年10月26日

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

https://huagongshe.com/reaction/276117

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon TetrachlorideHCID 5943—
反応物AnisoleHCID 7519—
反応物2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine N-methyl amideHCID 86757825—
触媒Mercuric acetateHCID 15337—
溶媒DichloromethaneHCID 6344—
生成物2-mercapto-pentanoyl-(L)-homophenylalanyl-(L)-phenylalanine-N-methyl amideHCID 5987874480.5%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06352976B1
出典データセットuspto-grants-2002_03
ORD IDord-27473199c8ff43b1ac82c772cd020e0b
出典メモuspto-grants-2002_03