Title of article
Efficient and selective synthesis of alkoxy substituted di(pyridin-2-yl)amines and N-arylpyridin-2-ylamines
Author/Authors
I.C Grig-Alexa، نويسنده , , Irina-Claudia and Simionescu، نويسنده , , Iuliana and Patriciu، نويسنده , , Oana-Irina and Massip، نويسنده , , Stéphane and Fînaru، نويسنده , , Adriana-Luminita and Jarry، نويسنده , , Christian and Léger، نويسنده , , Jean-Michel and Guillaumet، نويسنده , , Gérald، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2012
Pages
4
From page
1885
To page
1888
Abstract
The formation of alkoxy substituted di(pyridin-2-yl)amines and N-arylpyridin-2-ylamines by nitro group reduction is described. Unexpected substitution of ortho with the amino at C-6 was observed during the reduction using SnCl2·2H2O in different alcohols. The influence of the nature of the atom at the 3- and 5-positions of nitro-substituted di(pyridin-2-yl)amines and N-arylpyridin-2-ylamines was investigated.
Keywords
pyridines , Amines , Reduction , Stannous chloride dihydrate , Ortho position
Journal title
Tetrahedron Letters
Serial Year
2012
Journal title
Tetrahedron Letters
Record number
1880458
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