An efficient N-selective alkylation of primary aromatic amines in molten quaternary ammonium salts, as the solvent, under relatively mild and base-free conditions is presented. On the basis of the Kamlet–Taft parameters and the nucleophilicity of the IL (ionic liquid) anions, the influence of the ionic liquid was evaluated. This protocol was validated on a larger multigram scale and with the syntheses of bioactive heterocycles (e.g., 1,4-benzothiazine and quinoxalines) and new efficient MALDI matrixes.

Selective N-Alkylation of Arylamines with Alkyl Chloride in Ionic Liquids: Scope and Applications

Monopoli, Antonio;COTUGNO, PIETRO;CALVANO, COSIMA DAMIANA;CIMINALE, Francesco;NACCI, Angelo
2012-01-01

Abstract

An efficient N-selective alkylation of primary aromatic amines in molten quaternary ammonium salts, as the solvent, under relatively mild and base-free conditions is presented. On the basis of the Kamlet–Taft parameters and the nucleophilicity of the IL (ionic liquid) anions, the influence of the ionic liquid was evaluated. This protocol was validated on a larger multigram scale and with the syntheses of bioactive heterocycles (e.g., 1,4-benzothiazine and quinoxalines) and new efficient MALDI matrixes.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11586/128819
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