反应 #9969

ord-48980c3bc29d442994e424cd77e71dc8

反应方程式

NC1CCN2CCCC2C1
(±)-7-Amino-1,2,3,5,6,7,8,8a-octahydroindolizine
O=Cc1ccncc1
4-formylpyridine
O=S(=O)([O-])[O-].[Mg+2]
magnesium sulfate
C(=NC1CCN2CCCC2C1)c1ccncc1
title compound
收率 100.7%
C(=NC1CCN2CCCC2C1)c1ccncc1
(±)-7-(Pyridin-4-yl)methyleneamino-1,2,3,5,6,7,8,8a-octahydroindolizine
收率 100.7%

溶剂

反应条件

温度
70°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤At the end of this time, the reaction mixture was filtered
  2. 2
    其他to remove the catalyst
  3. 3
    浓缩the filtrate was concentrated by evaporation under reduced pressure

实验过程

(±)-7-Amino-1,2,3,5,6,7,8,8a-octahydroindolizine (4.91 g (35.0 mmol), prepared as described in 1)) was dissolved in toluene (95 ml). To the solution were added 4-formylpyridine (3.34 ml, 35.0 mmol) and anhydrous magnesium sulfate (3.75 g, 31.2 mmol), and the resulting mixture was stirred at 70° C. for 3 hours. At the end of this time, the reaction mixture was filtered to remove the catalyst and the filtrate was concentrated by evaporation under reduced pressure, to give the title compound (8.08 g) as a pale yellow oil (yield quantitative).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07091352B2uspto-grants-2006_08