Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/8943
Title: Carbon-SO3H catalyzed expedient synthesis of new spiro-[indeno[1,2-b]quinoxaline-[11,2′]-thiazolidine]-4′-ones as biologically important scaffold
Authors: Chaudhary, Archana
Keywords: 3' (4 methylphenyl)spiro(indeno[1,2 b]quinoxaline 11,2'[1,3]thiazolidine) 4' one;carbon;molecular scaffold;new drug;thiazolidine derivative;unclassified drug;Article;catalyst;cyclization;drug synthesis;drug transformation;electrophilicity;evaporation;feasibility study;filtration;Fourier transform infrared spectroscopy;nucleophilicity;reaction temperature;reaction time;room temperature;scanning electron microscopy;thin layer chromatography;X ray analysis;X ray crystallography;X ray diffraction
Issue Date: 2019
Publisher: Taylor and Francis Inc.
Citation: Singh, R., Ahmad Ganaie, S., Singh, A., & Chaudhary, A. (2019). Carbon-SO3H catalyzed expedient synthesis of new spiro-[indeno[1,2-b]quinoxaline-[11,2′]-thiazolidine]-4′-ones as biologically important scaffold. Synthetic Communications, 49(1), 80-93. doi:10.1080/00397911.2018.1542003
Abstract: In this report, we have described a convenient and eco-compatible approach for synthesis of new hybrid spiro[indeno[1,2-b]quinoxaline-[11,2′]-thiazolidine]-4′-ones (4a–k) via multi-component reaction of indeno[1,2-b]quinoxalinone, α-mercaptocarboxylic acids and various types of amines using urea-choline chloride as green deep eutectic solvent and carbon-SO3H as a solid acid catalyst. This new protocol produces a thiazolidine ring attached to indeno[1,2-b]quinoxaline through spiro carbon in good to excellent yields. The advantages of this protocol are avoidance of toxic and harmful catalyst and solvents further both catalyst and DES were recovered from the reaction mixture quantitatively and reused several times. Synthesized compounds were characterized on the basis of spectral and single crystal X-ray analysis. The prepared catalyst was characterized by FT-IR, SEM, and X-ray diffraction method. © 2019, © 2019 Taylor & Francis Group, LLC.
URI: https://doi.org/10.1080/00397911.2018.1542003
https://dspace.iiti.ac.in/handle/123456789/8943
ISSN: 0039-7911
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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