反应 #1365751

ord-610fc9f60210400f8ffb8f825c3ba128

反应方程式

CC(c1n[nH]c2cc([C@@H]3CN(Cc4ccccc4)C[C@@]3(C)CO)ccc12)C1CCCC1
solution
CC(c1n[nH]c2cc([C@@H]3CN(Cc4ccccc4)C[C@@]3(C)CO)ccc12)C1CCCC1
[(3S,4S)-4-(1-Cyclopentyl-3-ethyl(1H-indazol-6-yl))-3-methyl-1-benzylpyrrolidin-3-yl]methan-1-ol
CC(c1n[nH]c2cc([C@@H]3CNC[C@@]3(C)CO)ccc12)C1CCCC1
pyrrolidine
收率 71.0%
CC(c1n[nH]c2cc([C@@H]3CNC[C@@]3(C)CO)ccc12)C1CCCC1
[(3S,4S)-4-(1-Cyclopentyl-3-ethyl(1H-indazol-6-yl))-3-methylpyrrolidin-3-yl]methan-1-ol
收率 71.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Hydrogen was vigorously bubbled through the solution for 5 minutes
  2. 2
    其他the catalyst was removed by filtration through celite
  3. 3
    其他The solvent then was removed in vacuo

实验过程

To a stirred solution of Example 3 (25.5 mg; 0.0611 mmol) in 190 proof ethanol (2.0 mL) was added 10% Pd/C (5 mg; 20 wt. % catalyst). Hydrogen was vigorously bubbled through the solution for 5 minutes. The reaction was allowed to stir at room temperature for 2 hours, then the catalyst was removed by filtration through celite. The solvent then was removed in vacuo to provide the named pyrrolidine (14 mg; 71%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06444671B1uspto-grants-2002_09