Contact Us
Click Here

"ZnCl2 at MMT K-10 Catalysed Synthesis of 1,5-Benzodiazepine-2,4-diones from β-amino carbonyls", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.8, Issue 2, page no.743-751, February-2021, Available :http://www.jetir.org/papers/JETIR2102087.pdf

• Sagar Narayan Dakhane

1,5-benzodiazepine-2,4-diones are the most studied group of diazepine, which act as inhibitors of HIV-1 capsid assembly and reverse transcriptase. The benzodiazepine-2,4-dinone derivatives were prepared from β-amino carbonyl compounds by greener method using metal catalyst loaded on MMT K-10. The starting materials β-amino carbonyls were synthesized by multicomponent Mannich reaction at room temperature using 20 mol percentage of NH4Cl. Metal supported Montmorillonite K10-catalyzed reactions of various substituted β-amino carbonyls with OPDAs afforded 1,5-bezodiazapine-2,4-diones. Among the synthesized catalysts, the 10% Zn-K10 exhibited high conversion up to 90% and high selectivity up to 100% towards 1,5-bezodiazapine-2,4-diones

β-aminocarbonyls, 1,5 –benzodiazepine, MMT-K-10, impregnation method, OPDAs

"ZnCl2 at MMT K-10 Catalysed Synthesis of 1,5-Benzodiazepine-2,4-diones from β-amino carbonyls", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.8, Issue 2, page no. pp743-751, February-2021, Available at : http://www.jetir.org/papers/JETIR2102087.pdf