반응 #9969

ord-48980c3bc29d442994e424cd77e71dc8

반응 방정식

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
수율 100.7%
C(=NC1CCN2CCCC2C1)c1ccncc1
(±)-7-(Pyridin-4-yl)methyleneamino-1,2,3,5,6,7,8,8a-octahydroindolizine
수율 100.7%

용매

반응 조건

온도
70°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과At the end of this time, the reaction mixture was filtered
  2. 2
    기타to remove the catalyst
  3. 3
    농축the filtrate was concentrated by evaporation under reduced pressure

실험 절차

(±)-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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07091352B2uspto-grants-2006_08