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A One-pot process for the synthesis of Alkyne-3-tretrazolyl-tetrazolo [1,5-a] quinolines.
Sandra Cecilia Ramírez López, Murali Venkata Basavanag Unnamatla, María del Rocio Gámez Montaño *
1  Universidad de Guanajuato, División de Ciencias Naturales y Exactas, Departamento de Química

10.3390/ecsoc-22-05798
Abstract:

An efficient synthesis of alkyne-3-tetrazolyl-Tetrazolo[1,5-a] quinolone via a one-pot process: I-MCR Ugi-azide /SNAr/ ring-chain azido tautomerization under ecofriendly conditions. We report the one-pot synthesis of tris-heterocycles containing the tetrazolo[1,5-a]quinoline bound with 1,5-disubstituted-tetrazole (1,5-DS-T). The synthesis of this compounds can be of high interest for synthetic and medicinal chemistry because all the heterocycles are considered privilegied scaffolds and could lead to the discovery of novel bioactive molecules.

Keywords: Isocyanide based multicomponent reactions; Ugi-azide; Tetrazolo [1,5-a] quinolines; ring-chain azido tautomerization; one-pot process.
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