HRID133128

反应详情

EQUATION

反应方程式

HRID 133128 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of benzyl (5S)—N2,N2-bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-6-nitro-D-norleucinate from Step C (15.5 g, 26.8 mmol) and 10% Pd/C (12.0 g) in EtOH (175 mL), was hydrogenated at 55 psi for 18 h. An additional portion of 10% Pd/C (4.0 g) was added and the reaction mixture was hydrogenated at 55 psi for a further 18 h. The reaction mixture was filtered through Celite, washing with EtOH, and the filtrate was concentrated in vacuo to afford the title compound. MS: m/z=459 (M+1).

WORKUP

后处理

  1. waitthe reaction mixture was hydrogenated at 55 psi for a further 18 h
  2. filtrationThe reaction mixture was filtered through Celite
  3. washwashing with EtOH
  4. concentrationthe filtrate was concentrated in vacuo