Campestre Cristina, Keglevich György, Kóti János, Scotti Luca, Gasbarri Carla, Angelini Guido
Department of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara via dei Vestini 66100 Chieti Italy
Department of Organic Chemistry and Technology, Budapest University of Technology and Economics 1521 Budapest Hungary.
RSC Adv. 2020 Mar 25;10(21):12249-12254. doi: 10.1039/d0ra00833h. eCollection 2020 Mar 24.
A series of 2-anilinopyrimidines including novel derivatives has been obtained from 2-chloro-4,6-dimethylpyrimidine by aromatic nucleophilic substitution with differently substituted anilines under microwave conditions. The substituents had a significant impact on the course and efficiency of the reaction. The results reported herein demonstrate the efficacy of microwaves in the synthesis of the title heterocyclic compounds as compared to the results obtained with conventional heating. The 2-anilinopyrimidines described are of potential bioactivity.
通过在微波条件下用不同取代的苯胺进行芳香亲核取代反应,从2-氯-4,6-二甲基嘧啶中获得了一系列包括新型衍生物在内的2-苯胺基嘧啶。取代基对反应过程和效率有显著影响。本文报道的结果表明,与传统加热方法相比,微波在合成标题杂环化合物方面具有有效性。所述的2-苯胺基嘧啶具有潜在的生物活性。