Synthesis of Triazoloindazole Triones under Solvent-Free Condition using Cu(I) Coordinated to Vanillin-Isoniazid Supported Fe3O4/Silica Propyl as an Efficient and Magnetically Retrievable Nanocatalyst
Cu(I) coordinated to vanillin-isoniazid supported Fe3O4/silica propyl NPs were prepared and were analyzed by XRD, FT-IR, VSM, FE-SEM, TEM, and TGA-DTG. These nano catalysts were applied as an efficient and magnetically reusable nanocatalyst for the preparation of various derivatives of triazoloindazole triones and pyrazolyl-linked triazoloindazole triones under solvent-free condition. All of synthesized compounds were analyzed by NMR, FT-IR, and elemental analysis. This avenue offers many benefits such as productivity, fast reaction, and convenience for work and recovery. The catalyst is reusable for 8 runs by decantation using an efficient magnet without notable loss in activity.
Authors
- L. Zare Fekri
- Payam Nankali
- Romina Ataei Khorrami
- Taha Parkhondeh
Institutions
- National Iranian Oil Company (Iran) (IR)
- University of Toronto (CA)
- Iran Khodro (Iran) (IR)
- Payame Noor University (IR)
Publication Details
- Journal
- Russian Journal of Organic Chemistry
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1134/s1070428025602237
- Primary Topic
- Multicomponent Synthesis of Heterocycles
- Type
- article
- Field-Weighted Citation Impact
- 0.00