4.6 Article

Multicomponent Click Synthesis of New 1,2,3-Triazole Derivatives of Pyrimidine Nucleobases: Promising Acidic Corrosion Inhibitors for Steel

Journal

MOLECULES
Volume 18, Issue 12, Pages 15064-15079

Publisher

MDPI AG
DOI: 10.3390/molecules181215064

Keywords

nucleobases; multicomponent reaction; 1,2,3-triazoles; acidic corrosion; steel

Funding

  1. Consejo Nacional de Ciencia y Tecnologia, CONACyT [181448]
  2. SNI (Sistema Nacional de Investigadores)

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A series of new mono-1,2,3-triazole derivatives of pyrimidine nucleobases were synthesized by one-pot copper(I)-catalyzed 1,3-dipolar cycloaddition reactions between N-1-propargyluracil and thymine, sodium azide and several benzyl halides. The desired heterocyclic compounds were obtained in good yields and characterized by NMR, IR, and high resolution mass spectrometry. These compounds were investigated as corrosion inhibitors for steel in 1 M HCl solution, using electrochemical impedance spectroscopy (EIS) technique. The results indicate that these heterocyclic compounds are promising acidic corrosion inhibitors for steel.

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