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Thienopyrimidine–piperazine hybrids as multifunctional pharmacophores: design, synthesis, and biological evaluation

Aug 2026 · Phosphorus Sulfur and Silicon and the Related Elements · Vol 201, pp. 1554 - 1563 · 0 citations · 26 references

TL;DR

The results suggest that the thienopyrimidine–piperazine scaffold is a promising framework for the development of multifunctional therapeutic agents.

Abstract

Abstract A series of novel 5,6-dimethylthieno[2,3-d]pyrimidine-piperazine hybrids was rationally designed, synthesized, and evaluated to explore their potential as multifunctional bioactive agents. The target compounds were synthesized via nucleophilic substitution of 4-chloro-5,6-dimethylthieno[2,3-d]pyrimidine with structurally diverse substituted piperazines, affording the desired derivatives in good yields. Structural confirmation was achieved through elemental analysis and comprehensive spectroscopic techniques, which were consistent with the proposed molecular frameworks. Derivatives 4h and 4i showed the most potent antimicrobial activity, while 4f and 4g exhibited superior antioxidant effects. Compounds 4g, 4j, and 4k demonstrated comparatively higher anti-inflammatory activity. Structure–activity relationship (SAR) analysis revealed that electron-withdrawing groups enhance antimicrobial activity, whereas aromatic and electron-rich substituents favor antioxidant and anti-inflammatory responses. Although the activity was lower than that of standard drugs, several compounds displayed meaningful biological potential. These results suggest that the thienopyrimidine–piperazine scaffold is a promising framework for the development of multifunctional therapeutic agents. GRAPHICAL ABSTRACTDiagram of Thienopyrimidine-Piperazine core linked to antibacterial, antifungal, anti-inflammatory, and antioxidant activities with icons.The diagram showcases a central Thienopyrimidine-Piperazine core structure, with arrows pointing to four activity categories: Antibacterial (depicted by Gram-positive and Gram-negative icons), Antifungal (featuring Candida and Aspergillus), Anti-inflammatory (illustrating protein denaturation and COX inhibition), and Antioxidant (showcasing DPPH radical scavenging and OPPH). It includes sections for "Efficient Synthesis & Characterization" and "Broad Spectrum Biological Activities." The overall title emphasizes the multifunctional potential of these hybrids as antimicrobial, antioxidant, and anti-inflammatory agents.

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