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Microwave-assisted three-component domino reaction: Synthesis of indolodiazepinotriazoles

DOI: 10.3762/bjoc.9.41

Keywords: 2-alkynylindoles , azides , 1 , 3-dipolar cycloaddition , domino reaction , indolodiazepinotriazoles

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Abstract:

A microwave-assisted three-component protocol involving N-1 alkylation of 2-alkynylindoles with epichlorohydrin, ring opening of the epoxide with sodium azide, and an intramolecular Huisgen azide–internal alkyne 1,3-dipolar cycloaddition domino sequence has been described. The efficacy of the methodology has been demonstrated by treating various 2-alkynylindoles (aromatic/aliphatic) with epichlorohydrin and sodium azide furnishing annulated tetracyclic indolodiazepinotriazoles in satisfactory yields.

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