HRID655980

反应详情

EQUATION

反应方程式

HRID 655980 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of crude (2S,4R)-tert-butyl 4-(((9H-fluoren-9-yl)methoxy)carbonylamino)-2-((4-ethylphenylcarbamoyloxy)methyl)pyrrolidine-1-carboxylate in MeOH was added HCl (4 N in dioxane). The reaction was stirred at rt for 1 h and concentrated. The residue was dissolved in THF (10 mL). To this solution were added DIEA (469 μL, 2.7 mmol) and 2-chlorobenzylisocyanate. The mixture was stirred at rt for 1 h and concentrated. The residue was dissolved in 10 ml of 20% piperidine in DCM. The reaction mixture was stirred at rt for 15 min, concentrated and purified on RP-HPLC using a mixture of acetonitrile and H2O to give ((2S,4R)-4-amino-1-(2-chlorobenzylcarbamoyl)pyrrolidin-2-yl)methyl 4-ethylphenylcarbamate (210 mg, 53% for 4 steps). LRMS (M+H+) m/z 431.1.

WORKUP

后处理

  1. concentrationconcentrated
  2. dissolutionThe residue was dissolved in THF (10 mL)
  3. stirringThe mixture was stirred at rt for 1 h
  4. concentrationconcentrated
  5. dissolutionThe residue was dissolved in 10 ml of 20% piperidine in DCM
  6. stirringThe reaction mixture was stirred at rt for 15 min
  7. concentrationconcentrated
  8. custompurified on RP-HPLC
  9. additiona mixture of acetonitrile and H2O