Green and solid-phase synthesis of new dihydro-1,2,4]triazolo1,5-a]pyrimidine scaffolds by using poly-melamine-formaldehyde as a nitrogen-rich porous organocatalyst

Khaligh, Nader Ghaffari and Mihankhah, Taraneh (2022) Green and solid-phase synthesis of new dihydro-1,2,4]triazolo1,5-a]pyrimidine scaffolds by using poly-melamine-formaldehyde as a nitrogen-rich porous organocatalyst. Polycyclic Aromatic Compounds, 42 (3). pp. 942-950. ISSN 1040-6638, DOI https://doi.org/10.1080/10406638.2020.1756357.

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Abstract

This work presents a new catalytic application of porous poly-melamine-formaldehyde (mPMF) for the efficient synthesis of new dihydro-1,2,4]triazolo1,5-a]pyrimidines. According to the principals of green chemistry, the reaction was performed by the planetary ball milling process at ambient and neat conditions. The heterogeneous catalyst could be reused up to five runs with no reducing of catalytic efficiency. A variety of substituted dihydro-1,2,4]triazolo1,5-a]pyrimidines were obtained in good to excellent yields under eco-friendly conditions. This work revealed that bifunctional porous organic polymers (POPs) containing base sites and acceptor-donner hydrogen bonding groups, as well as high porosity could play a vital role in the promotion of the one-pot multicomponent reactions in the solid phase. The main merits of the current methodology include short reaction time, wide substrate-scope, and use of a metal-free heterogeneous organocatalyst, simple work-up process.

Item Type: Article
Funders: High Impact Research Grant Universiti of Malaya [Grant No: NANOCAT RU001-2018]
Uncontrolled Keywords: Porous material; Solid-phase synthesis; Heterogeneous catalysis; Multicomponent reactions; Sustainable chemistry
Subjects: H Social Sciences > H Social Sciences (General)
Divisions: Nanotechnology & Catalysis Research Centre
Depositing User: Ms. Juhaida Abd Rahim
Date Deposited: 10 Oct 2023 06:06
Last Modified: 10 Oct 2023 06:06
URI: http://eprints.um.edu.my/id/eprint/42487

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