Transition‐Metal‐Free Synthesis of 7‐Aminocoumarins from 7‐Hydroxycoumarins Using Multifunctional Reagent

Abstract We have successfully synthesized N‐substituted 7‐aminocoumarins by reacting 7‐hydroxycoumarins with amines using 5,6‐dichloro‐2,3‐dicyanopyrazine, a readily available multifunctional reagent. This reagent effectively brings both coupling partners into close proximity, facilitating dehydrative C─N coupling reactions under mild, metal‐free conditions. Our approach demonstrates a broad substrate scope and enables gram‐scale production.

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Publication Details

Journal
ChemistrySelect
Published
2025-02-01
DOI
https://doi.org/10.1002/slct.202404808
Citations
1
Primary Topic
Synthesis and Biological Evaluation
Type
article
Field-Weighted Citation Impact
0.94

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article

Transition‐Metal‐Free Synthesis of 7‐Aminocoumarins from 7‐Hydroxycoumarins Using Multifunctional Reagent

Pallavi Saha, Harish K. Indurthi, Samarpita Das, Deepak K. Sharma
1 citations
ChemistrySelect
Synthesis and Biological Evaluation
0.94
article

Transition‐Metal‐Free Synthesis of 7‐Aminocoumarins from 7‐Hydroxycoumarins Using Multifunctional Reagent

Pallavi Saha, Harish K. Indurthi, Samarpita Das, Deepak K. Sharma
article en
1 citations

Abstract

Abstract We have successfully synthesized N‐substituted 7‐aminocoumarins by reacting 7‐hydroxycoumarins with amines using 5,6‐dichloro‐2,3‐dicyanopyrazine, a readily available multifunctional reagent. This reagent effectively brings both coupling partners into close proximity, facilitating dehydrative C─N coupling reactions under mild, metal‐free conditions. Our approach demonstrates a broad substrate scope and enables gram‐scale production.

ChemistrySelectVol. 10(6)
Banaras Hindu University (IN)
Department of Biotechnology, Ministry of Science and Technology, India
Openalex Percentile: Top 29%
Synthesis and Biological Evaluation
0.94
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