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Indium Trichloride (InCl3) Catalyzed Synthesis of Fused 7‐Azaindole Derivatives Using Domino Knoevenagel‐Michael Reaction
Authors:Sakharam B. Dongare  Hemant V. Chavan  Datta N. Surwase  Pravin S. Bhale  Yoginath B. Mule  Babasaheb P. Bandgar
Affiliation:1. School of Chemical Sciences, Solapur University, Solapur‐413 255, Maharashtra, India;2. Department of Chemistry, A.S.P. College, Devrukh, Dist‐Ratnagiri‐415 804, Maharashtra, India
Abstract:An efficient and high yielding methodology developed for the synthesis of fused 7‐azaindole derivatives via one pot multicomponent assembly process of cyclic 1,3‐dicarbonyls with substituted aldehydes and 5‐amino‐1‐tert‐butyl‐1H‐pyrrole‐3‐carbonitrile. The transformation occurs via domino Knoevenagel‐ Michael reaction followed by intramolecular cyclization in the presence of catalytic amount of InCl3 (10 mol %). Mild reaction conditions, easy isolation of products, and good to excellent yields in a shorter period of time are the silent features of present methodology. Structures of all the newly prepared compounds have been corroborated by various spectroscopic methods.
Keywords:Indium trichloride  Fused 7‐azaindoles  Knoevenagel condensation  Michael addition  Domino reaction
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