反应 #1465651

反应方程式

2-[[2-(1-tert-butoxycarbonyl-3-methylbutylcarbamoyl)-4-fluorophenyldisulfanyl]-5-fluorobenzoylamino]-4-methylpentanoic acid tert-butyl ester

trifluoroacetic acid

→

title compound

2-[2-[2-(1-Carboxy-3-methylbutyl-carbamoyl)-4-fluorophenyldisulfanyl]-5-fluorobenzoylamino]-4-methyl-pentanoic acid

溶剂

anisole

dichloromethane

反应条件

后处理

1. 1
   其他The general method of Preparation 20
2. 2
   其他The crude product was recrystallized from methanol/water

实验过程

The general method of Preparation 20 was followed using [S-(R*,R*)]-2-[2-[[2-(1-tert-butoxycarbonyl-3-methylbutylcarbamoyl)-4-fluorophenyldisulfanyl]-5-fluorobenzoylamino]-4-methylpentanoic acid tert-butyl ester (1.8 g, 2.6 mmol) in 20 mL dichloromethane, anisole (2 mL), and 20 mL trifluoroacetic acid. The crude product was recrystallized from methanol/water to afford 0.9 g of the title compound.

来源