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Synthesis and Tactics of Organic Synthesis of 6-(5-mercapto-4R-4H-1,2,4-triazol-3-YL)pyrimidine-2,4(1H,3H)-dione Derivatives

Title: Synthesis and Tactics of Organic Synthesis of 6-(5-mercapto-4R-4H-1,2,4-triazol-3-YL)pyrimidine-2,4(1H,3H)-dione Derivatives
Authors: Yuriy Karpenko
Source: Chemistry Proceedings ; Volume 18 ; Issue 1 ; Pages: 46
Publisher Information: Multidisciplinary Digital Publishing Institute
Publication Year: 2025
Collection: MDPI Open Access Publishing
Subject Terms: pyrimidine-2,4(1 H ,3 H )-dione; 1,2,4-triazole; orotic acid; cyclocondensation
Description: Synthesis of 6-(5-mercapto-4R-4H-1,2,4-triazol-3-yl)pyrimidine-2,4(1H,3H)-dione derivatives offer a versatile platform for the development of new heterocyclic compounds. These molecules combine the biologically relevant 1,2,4-triazole ring, known for its antimicrobial and antioxidant properties, with a pyrimidine-2,4-dione core structurally related to vitamin B13 (orotic acid), essential in nucleic acid metabolism. This dual structure opens a wide spectrum of synthetic possibilities, particularly in heterocyclization reactions. The synthesis usually begins with the formation of the triazole ring through cyclocondensation of thiosemicarbazides with appropriate carbonyl precursors, followed by functionalization of the thiol group via S-alkylation or S-arylation.
Document Type: text
File Description: application/pdf
Language: English
DOI: 10.3390/ecsoc-29-26848
Availability: https://doi.org/10.3390/ecsoc-29-26848
Rights: https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.6A2B61A3
Database: BASE