Rapid Access Synthesis of Quinoline, Chromene, Thiochromene Benzimidazol-Ylideneamines and Benzimidazolones via Traceless Tandem Transformation Under Microwave Irradiation on Ionic Liquid Support
Journal Title: UNKNOWN - Year 2018, Vol 8, Issue 8
Abstract
A fast and efficient protocol have explored to access the various benzimidazole constituted quinoline, chromene, thiochromenyldenamines and ones under microwave irradiation on ionic liquid support. Ionic liquid supported 4-floro3-nitrobenzoicacid has been used as a structural building block to generate these structural frameworks. After subsequent transformation the benzimidazole constituted cyanoacetic acid has been used as a molecular scaffold to generate various structural motifs. By taking the benzimidazole constituted cyanoacetic acid treated with various 2-substituted hydroxyl, amino and thiobanzaldehydes in order to get the described decorated structural scaffolds in the presence of organic base such as triethylamine. Under the same reaction conditions by leave the product and the cleavage of product from the support occurred sequence of transformations in traceless tandem manner. The same reaction under the hydrous conditions the imine hydrolysis leads to formation of quinoline, chromene, thiochromene benzimidazolones was described. The final compounds have been obtained high yield and purity making this procedure facile, practical, and rapid to execute.
Authors and Affiliations
Suman Thummanagoti, Chih Hau Chen, Chung Ming Sun
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