HRID502693

反应详情

EQUATION

反应方程式

HRID 502693 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a 100 mL RBF was added (S)-tert-butyl methyl(1-(2-nitro-4-(trifluoromethyl)phenyl)piperidin-3-yl)carbamate (1.75 g, 4.34 mmol) and palladium, 10 wt. % on activated carbon wet (0.923 g, 0.868 mmol) under nitrogen. MeOH was added via syringe, and the atmosphere was purged with hydrogen from a balloon. The reaction was allowed to stir rapidly under hydrogen for 8 h. The flask was purged with nitrogen, filtered through celite, rinsing with 100 mL MeOH, and concentrated to give (S)-tert-butyl 1-(2-amino-4-(trifluoromethyl)phenyl)piperidin-3-yl(methyl)carbamate as a gray solid. MS m/z=374 [M+H]+. Calc'd for C18H26F3N3O2: 373.

WORKUP

后处理

  1. customthe atmosphere was purged with hydrogen from a balloon
  2. customThe flask was purged with nitrogen
  3. filtrationfiltered through celite
  4. washrinsing with 100 mL MeOH
  5. concentrationconcentrated