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Rapid, Microwave Accelerated Synthesis of [1,2,4]Triazolo[3,4-b][1,3,4]oxadiazoles from 4-Acylamino-1,2,4-Triazoles.


ABSTRACT: 1,2,4-Triazoles and 1,3,4-oxadiazoles are prevalent moieties in pharmaceutical agents, yet fused [1,2,4]-triazolo[3,4-b][1,3,4]oxadiazoles are surprisingly under-represented for both synthesis and biological application. We report a rapid, two-step synthesis of [1,2,4]-triazolo[3,4-b][1,3,4]oxadiazoles from commercial 4-amino-1,2,4-triazoles that is highlighted by a microwave accelerated intramolecular cyclization to generate the fused ring system. Our efforts to optimize reaction conditions and elucidate reaction mechanism are also described.

SUBMITTER: Breunig SL 

PROVIDER: S-EPMC5271595 | biostudies-literature | 2016 Sep

REPOSITORIES: biostudies-literature

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Rapid, Microwave Accelerated Synthesis of [1,2,4]Triazolo[3,4-<i>b</i>][1,3,4]oxadiazoles from 4-Acylamino-1,2,4-Triazoles.

Breunig Stesphanie L SL   Olson Margaret E ME   Harki Daniel A DA  

Tetrahedron letters 20160729 36


1,2,4-Triazoles and 1,3,4-oxadiazoles are prevalent moieties in pharmaceutical agents, yet fused [1,2,4]-triazolo[3,4-<i>b</i>][1,3,4]oxadiazoles are surprisingly under-represented for both synthesis and biological application. We report a rapid, two-step synthesis of [1,2,4]-triazolo[3,4-<i>b</i>][1,3,4]oxadiazoles from commercial 4-amino-1,2,4-triazoles that is highlighted by a microwave accelerated intramolecular cyclization to generate the fused ring system. Our efforts to optimize reaction  ...[more]

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