University of Groningen , Department of Drug Design, Antonius Deusinglaan 1 9713 AV, Groningen, The Netherlands.
Jagiellonian University , Faculty of Chemistry, Department of Crystal Chemistry and Crystal Physics, Biocrystallography Group, Ingardena 3, 30-060, Kraków, Poland.
Org Lett. 2017 Feb 3;19(3):642-645. doi: 10.1021/acs.orglett.6b03807. Epub 2017 Jan 19.
The morpholine and piperazine with their remarkable physical and biochemical properties are popular heterocycles in organic and medicinal chemistry used in rational property design. However, in the majority of cases these rings are added to an existing molecule in a building block approach thus limiting their substitution pattern and diversity. Here we introduce a versatile de novo synthesis of the morpholine and piperazine rings using multicomponent reaction chemistry. The large scale amenable building blocks can be further substituted at up to four positions, making this a very versatile scaffold synthesis strategy. Our methods thus fulfill the increasing demand for novel building block design and nontraditional scaffolds which previously were not accessible.
具有显著物理和生化性质的吗啉和哌嗪是有机和药物化学中常用的杂环,用于合理的性质设计。然而,在大多数情况下,这些环是作为构建块添加到现有分子中,从而限制了它们的取代模式和多样性。在这里,我们介绍了一种使用多组分反应化学的吗啉和哌嗪环的通用从头合成方法。这些易于扩大规模的构建块可以在多达四个位置进一步取代,这使其成为一种非常通用的支架合成策略。因此,我们的方法满足了对新型构建块设计和以前无法获得的非传统支架的日益增长的需求。