S<sub>N</sub>Ar Reactions on 2-Amino-4,6-dichloropyrimidine-5-carbaldehyde

We report the experimental results of unexpected aromatic nucleophilic substitution reaction products on 2-amino-4,6-dichloropyrimidine-5-carbaldehyde. The isolated compounds are products of amination, solvolysis, and condensation processes under mild and environmentally friendly conditions, due to...

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Bibliographic Details
Main Authors: Jorge Trilleras, Alfredo Pérez-Gamboa, Jairo Quiroga
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Molbank
Subjects:
Online Access:https://www.mdpi.com/1422-8599/2022/3/M1426
Description
Summary:We report the experimental results of unexpected aromatic nucleophilic substitution reaction products on 2-amino-4,6-dichloropyrimidine-5-carbaldehyde. The isolated compounds are products of amination, solvolysis, and condensation processes under mild and environmentally friendly conditions, due to the influence of structural factors of the starting pyrimidine and a high concentration of alkoxide ions. This method allows the building of pyrimidine-based compound precursors of <i>N</i>-heterocyclic systems.
ISSN:1422-8599