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Unexpected Formation of 5‐Nitro‐1H‐benzimidazoles by Nucleophilic Recyclization of 1‐Methyl‐5‐nitropyridinium Salts
Authors:Galina P Sagitullina  Anna K Garkushenko  Alexey N Novikov  Reva S Sagitullin
Institution:Department of Organic Chemistry, F. M. Dostoevsky Omsk State University, Omsk, Russian Federation
Abstract:The synthesis of substituted 5‐nitro‐2‐phenyl‐1H‐benzimidazoles has been described via domino anionic process rearrangement of 3‐benzoylamino‐1,2‐dimethyl‐5‐nitropyridinium salts in the presence of NaOH water–alcohol solution. Substituted N‐benzoyl‐o‐phenylenediamines was obtained via recyclization of 3‐benzoylamino‐1,2‐dimethyl‐5‐nitropyridinium salts in the presence of aqueous methylamine solution.
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