Synthesis of Pyrido[2,3-d]pyrimidine Carbodithioates Using Deep Eutectic Solvent as Recyclable Media and Three-Component Reaction

A facile, three-component one-pot synthesis of a combinatorial library of pyrido[2,3- d]pyrimidines by condensation of easily accessible β-oxodithioesters with 1,3-dimethyl-6-amino uracil and aldehydes under deep eutectic solvent medium is achieved. The yields of the desired products are good to excellent, irrespective of the steric and electronic nature of the substituents. The advantages of operational simplicity, economic viability, generality, and atom economy, together with its ecologically benign nature, make this protocol a very efficient alternative to literature methods. These compounds contain reactive functionalities for further ring annulation reactions and thus can be utilized as building blocks for complex natural products.

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Publication Details

Journal
Letters in Organic Chemistry
Published
2024-12-12
DOI
https://doi.org/10.2174/0115701786362985241206081037
Primary Topic
Synthesis of heterocyclic compounds
Type
article
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article

Synthesis of Pyrido[2,3-d]pyrimidine Carbodithioates Using Deep Eutectic Solvent as Recyclable Media and Three-Component Reaction

Mayanglambam Maneeta Devi, Ramesh Singh, Okram Mukherjee Singh, Narinder Singh et al.
Letters in Organic Chemistry
Synthesis of heterocyclic compounds
article

Synthesis of Pyrido[2,3-d]pyrimidine Carbodithioates Using Deep Eutectic Solvent as Recyclable Media and Three-Component Reaction

Mayanglambam Maneeta Devi, Ramesh Singh, Okram Mukherjee Singh, Narinder Singh, Langpoklakpam Gellina Chanu
article en

Abstract

A facile, three-component one-pot synthesis of a combinatorial library of pyrido[2,3- d]pyrimidines by condensation of easily accessible β-oxodithioesters with 1,3-dimethyl-6-amino uracil and aldehydes under deep eutectic solvent medium is achieved. The yields of the desired products are good to excellent, irrespective of the steric and electronic nature of the substituents. The advantages of operational simplicity, economic viability, generality, and atom economy, together with its ecologically benign nature, make this protocol a very efficient alternative to literature methods. These compounds contain reactive functionalities for further ring annulation reactions and thus can be utilized as building blocks for complex natural products.

Letters in Organic ChemistryVol. 22(5)
Manipur University (IN)
Openalex Percentile: Top 83%
Synthesis of heterocyclic compounds
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