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Updated: Jan 21, 2026

Preparation of Binary and Ternary Deep Eutectic Systems
Published on: October 31, 2019
Multicomponent Approach to Hydantoins and Thiohydantoins Involving a Deep Eutectic Solvent.
Sambasivarao Kotha1, Naveen K Gupta1, Vikas R Aswar1
1Department of Chemistry, Indian Institute of Technology, Bombay, Powai, Mumbai, 400 076, India.
A novel three-component reaction efficiently synthesizes diverse hydantoins and thiohydantoins using deep eutectic solvents. This method provides a straightforward route to valuable 5-amino-1,3-dialkyl-substituted compounds in good yields.
Area of Science:
- Organic Chemistry
- Green Chemistry
Background:
- Hydantoins and thiohydantoins are important heterocyclic compounds with diverse biological activities.
- Efficient synthesis of these scaffolds is crucial for drug discovery and development.
- Traditional synthetic methods often involve harsh conditions or multiple steps.
Purpose of the Study:
- To develop an efficient and green synthetic strategy for diverse hydantoins and thiohydantoins.
- To utilize deep eutectic solvents as both reaction medium and reactant source.
- To provide a facile access to 5-amino-1,3-dialkyl-substituted hydantoins and thiohydantoins.
Main Methods:
- A three-component reaction strategy was employed.
- Deep eutectic solvent systems were utilized, with N,N'-dimethyl urea or N,N'-dimethyl thiourea and l-(+)-tartaric acid serving dual roles.
- The reaction conditions were optimized for yield and purity.
Main Results:
- The developed method efficiently synthesized a range of hydantoins and thiohydantoins.
- Good yields were obtained for the target 5-amino-1,3-dialkyl-substituted compounds.
- The use of deep eutectic solvent facilitated a greener and more efficient process.
Conclusions:
- This study presents an efficient and environmentally friendly synthetic route to hydantoins and thiohydantoins.
- The three-component reaction in deep eutectic solvent offers a practical approach for accessing valuable heterocyclic compounds.
- The methodology holds promise for scalable synthesis in medicinal chemistry.
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