HRID723135

反应详情

EQUATION

反应方程式

HRID 723135 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a solution of ({3′-[5-(tert-butoxycarbonylamino-imino-methyl)-2-methylsulfanyl-thiophene-3-sulfonyl]-2-methyl-biphenyl-4-ylamino}-methyl)phosphonic acid diethyl ester (38 mg, 0.057 mmol) in DCM (1.2 mL) at 0° C. was added iodotrimethylsilane (25 μL) over 3 minutes period. After 1 h at 0° C., H2O was added. The mixture was stirred for 30 minutes, and then concentrated to give a brown solid. The solid was dissolved in MeOH (1.32 mL), 20% HCl was added, and stirred at ambient temperature for 3 h. The mixture was concentrated to give a brown solid. To this solid was added TFA/DCM (1:1, 3 mL) and stirred at ambient temperature for 40 minutes. The reaction mixture was then concentrated and purified by HPLC (C18 column, 10–70% CH3CN over 30 minutes) to give the title compound (11 mg, 38% yield) as a white solid.

WORKUP

后处理

  1. concentrationconcentrated
  2. customto give a brown solid
  3. stirringstirred at ambient temperature for 3 h
  4. concentrationThe mixture was concentrated
  5. customto give a brown solid
  6. stirringstirred at ambient temperature for 40 minutes
  7. concentrationThe reaction mixture was then concentrated
  8. custompurified by HPLC (C18 column, 10–70% CH3CN over 30 minutes)