1184635-94-6Relevant academic research and scientific papers
N-Propyl benzoguanamine sulfonic acid supported on magnetic Fe3O4 nanoparticles: A novel and efficient magnetically heterogeneous catalyst for the synthesis of 1,8-dioxo-decahydroacridine derivatives
Gholami Dehbalaei, Masoumeh,Foroughifar, Naser,Pasdar, Hoda,Khajeh-Amiri, Alireza
, p. 327 - 335 (2018)
In this study, N-propyl-benzoguanamine-SO3H-stabilized magnetic nanoparticles were prepared as a new heterogeneous acid catalyst in accordance with the principles of green chemistry. The new catalyst is used for the synthesis of derivatives of
Synthesis, characterization and application of Fe3O4@Silicapropyl@vaniline-covalented isoniazid-copper(I) nanocomposite as a new, mild, effective and magnetically recoverable Lewis acid catalyst for the synthesis of acridines and novel azoacridines
Fekri, Leila Zare,Nikpassand, Mohammad,Torabi, Mogharab
, (2021/11/01)
Fe3O4@Silicapropyl@vaniline-covalented isoniazid-copper(I) nanocomposite was synthesized as a novel heterogeneous catalyst and was characterized by FT-IR, EDX, XRD, FESEM, TEM, zeta potential, VSM and TGA-DTG. The strategy relies on the covalently bonding of vaniline to Fe3O4@silicapropyl followed by the condensation reaction of aldehyde moiety of vaniline in the structure of catalyst with isoniazid drug (NH2 moiety). Finally, complexation process in pyridine ring of isoniazid with CuCl lead to Fe3O4@Silicapropyl@vaniline-covalented isoniazide-copper(I) nanocomposite. This novel nanocatalyst was applied as a green, and effective nanocatalyst for the mild synthesis of acridines and azoacridines via multicomponent reaction of various aromatic aldehydes, dimedone and various anilines or azolinked aniline under solvent-free conditions. The products were characterized by FT-IR, NMR and CHN analysis. This new protocol has benefits such as high yields, short reaction time, easy work-up and processing, eco-friendly and green aspects of chemistry. Also, the nanocatalyst is a magnetically recoverable catalyst and reused for six runs without decrease the efficiency.
A convenient and efficient one-pot method for the synthesis of novel acridine-calix[4]arene derivatives as new DNA binding agents via multicomponent reaction
Mirza-Aghayan, Maryam,Yarmohammadi, Masoud,Zadmard, Reza,Boukherroub, Rabah
, p. 442 - 449 (2014/06/09)
A new approach is applied for the synthesis of novel acridine-calix[4]arene derivatives via a multicomponent reaction. These compounds have been characterised by 1H NMR, 13C NMR and HR-MS. Our binding studies between acridine-functio
Fe3+-montmorillonite: An efficient solid catalyst for one-pot synthesis of decahydroacridine derivatives
Luo, Haitang,Kang, Yuru,Nie, Hongyun,Yang, Liming
experimental part, p. 1280 - 1285 (2009/12/04)
Fe3+-montmorillonite was used as a solid acidic catalyst for the synthesis of decahydroacridine derivatives through the condensation of aromatic aldehydes, dimedone and aniline in ethanol. The influence of reaction time, reaction temperature, and the amount of catalyst were studied. All the compounds were characterized by IR, Mp, 1H NMR and 13C NMR analysis.
