One-Pot Multicomponent Synthesis of Uracil Derivatives and Their Antiviral Activity

Objective: The development of effective antiviral agents targeting whitefly-transmitted begomoviruses using a one-pot multicomponent reaction (MCR) approach. Methods: The synthesis was performed via a one-pot multicomponent reaction of aryl aldehydes, thiourea, and ethyl cyanoacetate in an ethanolic solution of potassium carbonate. The compounds were characterized using 1H, 13C NMR, FT-IR spectroscopy, and mass spectrometry. In vivo antiviral studies of the resulting compounds were conducted against whitefly-transmitted begomovirus using simultaneous, protective, and curative approaches. Results and Discussion: The results revealed that the synthesized derivative 6-(4-chlorophenyl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile IVa exhibited the best antiviral activity at 125 µg/mL in the protective approach. Conclusions: The synthesized compound IVa shows promising antiviral activity and could be considered for further development.

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Publication Details

Journal
Russian Journal of Bioorganic Chemistry
Published
2025-12-01
DOI
https://doi.org/10.1134/s1068162025600527
Primary Topic
Multicomponent Synthesis of Heterocycles
Type
article
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article

One-Pot Multicomponent Synthesis of Uracil Derivatives and Their Antiviral Activity

Divya Utreja, Kunal Jain, Arvind Sharma, Shivali Sharma
Russian Journal of Bioorganic Chemistry
Multicomponent Synthesis of Heterocycles
article

One-Pot Multicomponent Synthesis of Uracil Derivatives and Their Antiviral Activity

Divya Utreja, Kunal Jain, Arvind Sharma, Shivali Sharma
article en

Abstract

Objective: The development of effective antiviral agents targeting whitefly-transmitted begomoviruses using a one-pot multicomponent reaction (MCR) approach. Methods: The synthesis was performed via a one-pot multicomponent reaction of aryl aldehydes, thiourea, and ethyl cyanoacetate in an ethanolic solution of potassium carbonate. The compounds were characterized using 1H, 13C NMR, FT-IR spectroscopy, and mass spectrometry. In vivo antiviral studies of the resulting compounds were conducted against whitefly-transmitted begomovirus using simultaneous, protective, and curative approaches. Results and Discussion: The results revealed that the synthesized derivative 6-(4-chlorophenyl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile IVa exhibited the best antiviral activity at 125 µg/mL in the protective approach. Conclusions: The synthesized compound IVa shows promising antiviral activity and could be considered for further development.

Russian Journal of Bioorganic ChemistryVol. 51(6)
Punjab Agricultural University (IN)
Openalex Percentile: Top 72%
Multicomponent Synthesis of Heterocycles
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