Volume 32, Issue 45
Isocyclic Compounds
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ChemInform Abstract: Desymmetrization Reactions: A Convenient Synthesis of Aromatic Diamide Diamines.

Claude Picard

Claude Picard

Lab. Synth. Physicochim. Mol. Interet Biol., Univ. Paul Sabatier, F-31062 Toulouse, Fr.

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Nathalie Arnaud

Nathalie Arnaud

Lab. Synth. Physicochim. Mol. Interet Biol., Univ. Paul Sabatier, F-31062 Toulouse, Fr.

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Pierre Tisnes

Pierre Tisnes

Lab. Synth. Physicochim. Mol. Interet Biol., Univ. Paul Sabatier, F-31062 Toulouse, Fr.

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First published: 23 May 2010

Abstract

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ChemInform Abstract

The synthesis of various diamine diamides (III) derived from diaminobenzenes is described, involving their reaction with bis(thiazolidinethiones) (I) under mild reaction conditions. When substituted diaminobenzene derivatives like (IV) are used, the amidation reactions proceed with exclusive regioselectivity (product structure is not given). 2,3-Diaminonaphthalene does not undergo amidation reaction, probably due to its low nucleophilicity.

chemical structure image

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