Abstract

In vinyl nucleophilic substitution (SNvin) with the hydrochlorides or 4-toluenesulfonates of primary arylamines 1-alkyl-3-alkylaminopyrrole-2,5-diones form the corresponding 1-alkyl-3-arylaminopyrrole-2,5-diones, which are also produced in situ from the corresponding arylaminofumarates and primary alkylamines.

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