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Three-component sequential synthesis of N,N′-disubstituted 5-arylidenedihydropyrimidine-2,4-dione
Authors:Maria Cristina BellucciAlessandro Volonterio
Institution:a Dipartimento di Scienze Molecolari Agroalimentari, Università degli Studi di Milano, via Celoria 2, 20133 Milano, Italy
b Department of Chemistry, Materials and Chemical Engineer ‘Giulio Natta’, Politecnico di Milano, via Mancinelli 7, 20131 Milano, Italy
Abstract:A three-component sequential process consisting in (1) in situ formation of carbodiimides by Staudinger reaction, (2) reaction with 2-(bromomethyl)-3-aryl-2-propenoic acids, and (3) final cyclization of the resulting N-acylurea intermediates in order to obtain the synthesis of an array of N,N′-disubstituted 5-arylidenedihydropyrimidine-2,4-dione under mild conditions is presented.
Keywords:Multi-component  Sequential synthesis  Carbodiimides  Dihydropyrimidine-2  4-dione  N-Acylurea
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