Literature DB >> 15877477

Formation of 4-aminopyrimidines via the trimerization of nitriles using focused microwave heating.

Ian R Baxendale1, Steven V Ley.   

Abstract

A series of substituted aliphatic nitriles have been trimerized to their corresponding pyrimidine structures under solvent-free conditions in the presence of catalytic quantities of potassium tert-butoxide using a focused microwave reactor. Multigram quantities of the corresponding 4-aminopyrimidines have been prepared in high yields and purity following a simple and scaleable protocol.

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Year:  2005        PMID: 15877477     DOI: 10.1021/cc049826d

Source DB:  PubMed          Journal:  J Comb Chem        ISSN: 1520-4766


  3 in total

1.  The flow synthesis of heterocycles for natural product and medicinal chemistry applications.

Authors:  Marcus Baumann; Ian R Baxendale; Steven V Ley
Journal:  Mol Divers       Date:  2010-10-20       Impact factor: 2.943

Review 2.  Advances in microwave-assisted combinatorial chemistry without polymer-supported reagents.

Authors:  Rafael Martínez-Palou
Journal:  Mol Divers       Date:  2006-08-01       Impact factor: 2.943

3.  Temperature controlled condensation of nitriles: efficient and convenient synthesis of β-enaminonitriles, 4-aminopyrimidines and 4-amidinopyrimidines in one system.

Authors:  Yinghua Li; Yingzu Zhu; Shiqun Xiang; Weibin Fan; Jiang Jin; Deguang Huang
Journal:  RSC Adv       Date:  2020-02-12       Impact factor: 3.361

  3 in total

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