» Articles » PMID: 30141796

Nucleophilic Amination of Methoxypyridines by a Sodium Hydride-iodide Composite

Overview
Specialty Chemistry
Date 2018 Aug 25
PMID 30141796
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

A new protocol for nucleophilic amination of methoxypyridines and their derivatives was developed using sodium hydride (NaH) in the presence of lithium iodide (LiI). The method offers a concise access to various aminopyridines which are potentially of medicinal interest.

Citing Articles

LiCl-promoted amination of β-methoxy amides (γ-lactones).

Zhao R, Zeng B, Jia W, Zhao H, Shen L, Wang X RSC Adv. 2022; 10(57):34938-34942.

PMID: 35514391 PMC: 9056935. DOI: 10.1039/d0ra07170f.


Aggregation and Solvation of Sodium Hexamethyldisilazide: Across the Solvent Spectrum.

Woltornist R, Collum D J Org Chem. 2021; 86(3):2406-2422.

PMID: 33471993 PMC: 8011853. DOI: 10.1021/acs.joc.0c02546.


Cation Radical-Accelerated Nucleophilic Aromatic Substitution for Amination of Alkoxyarenes.

Venditto N, Nicewicz D Org Lett. 2020; 22(12):4817-4822.

PMID: 32484681 PMC: 7476680. DOI: 10.1021/acs.orglett.0c01621.


Concerted Nucleophilic Aromatic Substitution Reactions.

Rohrbach S, Smith A, Pang J, Poole D, Tuttle T, Chiba S Angew Chem Int Ed Engl. 2019; 58(46):16368-16388.

PMID: 30990931 PMC: 6899550. DOI: 10.1002/anie.201902216.