反应 #2298644

ord-f5e608738e7d4609bb79674cc2701688

反应方程式

CCc1nc(C)cc(=O)n1CCOc1ccc([N+](=O)[O-])cc1
4-[2-[2-ethyl-4-methyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]nitrobenzene
[H][H]
hydrogen
CCc1nc(C)cc(=O)n1CCOc1ccc(N)cc1
title compound
收率 70.0%
CCc1nc(C)cc(=O)n1CCOc1ccc(N)cc1
4-[2-[2-Ethyl-4-methyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]aniline
收率 70.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤The mixture was filtered through a bed of celite
  2. 2
    洗涤washed with dioxane
  3. 3
    其他evaporated to dryness under reduced pressure

实验过程

A solution of 4-[2-[2-ethyl-4-methyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]nitrobenzene (1.0 g, 3.3 mmol) (obtained from preparation 20) in 1,4-dioxane (20 ml) was reduced with hydrogen in the presence of 10% palladium on charcoal (100 mg) at 30 psi for 16 h. The mixture was filtered through a bed of celite and washed with dioxane and evaporated to dryness under reduced pressure to yield the title compound (625 mg, 70%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE039266E1uspto-grants-2006_09