Department of Chemistry & Pharmaceutical Sciences and Amsterdam Institute for Molecules Medicines and Systems (AIMMS), VU University Amsterdam , De Boelelaan 1083, 1081 HV Amsterdam, The Netherlands.
J Org Chem. 2013 Oct 18;78(20):10469-75. doi: 10.1021/jo401924h. Epub 2013 Oct 8.
Isocyanides have emerged as valuable C1 building blocks in palladium catalysis. Their potential has, however, mainly been exploited for the synthesis of amidines and amidine-containing heterocycles. To illustrate the broader applicability of isocyanides, we have recently developed a novel oxidative coupling of diamines and isocyanides furnishing valuable guanidine-containing heterocycles. We here report the extension of this protocol to the coupling of anthranilic acids and isocyanides leading to medicinally relevant 2-aminobenzoxazinones. This is a particularly challenging substrate class for this reaction due to the possibility of undesired decarboxylative pathways and the susceptibility of the products to nucleophilic attack. Therefore, this work underlines the generality and broad potential of the oxidative coupling of bisnucleophiles and isocyanides, facilitating the further implementation of this chemistry in library design.
异氰化物已成为钯催化中有用的 C1 构建块。然而,它们的潜力主要用于合成脒和含脒的杂环化合物。为了说明异氰化物的更广泛适用性,我们最近开发了一种新型的二胺和异氰化物的氧化偶联反应,可提供有价值的胍基含杂环化合物。我们在此报告了该方案的扩展,用于芳基丙氨酸和异氰化物的偶联,得到具有药物相关性的 2-氨基苯并恶嗪酮。由于可能存在不希望的脱羧途径以及产物对亲核攻击的敏感性,因此对于该反应来说,该底物类是特别具有挑战性的。因此,这项工作突出了双亲核试剂和异氰化物的氧化偶联的通用性和广泛潜力,促进了该化学在文库设计中的进一步应用。