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Three-Component Cascade Reaction of 1,1-Enediamines, N,N-Dimethylformamide Dimethyl Acetal, and 1,3-Dicarbonyl Compounds: Selective Synthesis of Diverse 2-Aminopyridine Derivatives.


ABSTRACT: A novel approach has been developed for the synthesis of three kinds of highly functionalized 2-aminopyridine derivatives (APDs) through a three-component reaction of 1,1-enediamines (EDAMs) 1, N,N-dimethylformamide dimethyl acetal (DMF-DMA) 2, and 1,3-dicarbonyl compounds 3-5 via a base-promoted cascade reaction, producing the desired products in good to excellent yields. This method represents a route to obtain a novel class of APDs in a concise, rapid, and practical manner. This approach is particularly attractive because of the following features: low cost, mild temperature, atom economy, high yields, and potential biological activity of the product.

SUBMITTER: Zi QX 

PROVIDER: S-EPMC6648487 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Three-Component Cascade Reaction of 1,1-Enediamines, <i>N</i>,<i>N</i>-Dimethylformamide Dimethyl Acetal, and 1,3-Dicarbonyl Compounds: Selective Synthesis of Diverse 2-Aminopyridine Derivatives.

Zi Quan-Xing QX   Yan Sheng-Jiao SJ   Yang Chang-Long CL   Li Kun K   Lin Jun J  

ACS omega 20190207 2


A novel approach has been developed for the synthesis of three kinds of highly functionalized 2-aminopyridine derivatives (APDs) through a three-component reaction of 1,1-enediamines (EDAMs) <b>1</b>, <i>N</i>,<i>N</i>-dimethylformamide dimethyl acetal (DMF-DMA) <b>2</b>, and 1,3-dicarbonyl compounds <b>3</b>-<b>5</b> via a base-promoted cascade reaction, producing the desired products in good to excellent yields. This method represents a route to obtain a novel class of APDs in a concise, rapid  ...[more]

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2011-10-06 | GSE32593 | GEO