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Synthesis 2019; 51(21): 4034-4042
DOI: 10.1055/s-0037-1611901
DOI: 10.1055/s-0037-1611901
paper
Combining Amines and 3-(2-Pyridyl)-[1,2,3]Triazolo[1,5-a]pyridine: An Easy Access to New Functional Polynitrogenated Ligands
This work was financially supported by the Ministerio de Economia, Industria y Competitividad (CONSOLIDER CTQ2017-90852-REDC), Generalitat Valenciana (Prometeo/2015/002) and the Universitat de València (Spain) (UV-INV-AE 15-332846).
Further Information
Publication History
Received: 22 May 2019
Accepted after revision: 03 July 2019
Publication Date:
07 August 2019 (online)
Abstract
Triazolopyridine-pyridine amine ligands are easily obtained by means of either thermal- or copper(II)-mediated reactions. Starting from a readily accessible iodo derivative of triazolopyridine-pyridine and different amines, this new family of compounds combines aromatic and aliphatic nitrogen atoms with promising coordinating properties. Furthermore, chemical derivatization of a new triazolopyridine-pyridine diamine compound, N1-[6-([1,2,3]triazolo[1,5-a]pyridin-3-yl)pyridin-2-yl]ethan-1,2-diamine, allows the preparation of several remote-pyridine-containing ligands.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0037-1611901.
- Supporting Information
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For the Ullmann–Goldberg reaction, see:
For the Buchwald–Hartwig cross-coupling reaction, see:
More specifically, the aryl halide amination reactions have been described by: