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作为潜在抗菌剂的恶唑烷酮的简便合成

Facile Synthesis of Oxazolidinones as Potential Antibacterial Agents.

作者信息

Els Secret P, Govender Kimberleigh B, Sokhela Mxolisi K, Bhatt Nilay, Reddy Nakita, Kruger Hendrik G, Arvidsson Per I, Gunosewoyo Hendra, Govender Thavendran, Naicker Tricia

机构信息

Discipline of Pharmaceutical Sciences, Catalysis and Peptide Research Unit, University of KwaZulu-Natal, Durban, 4000, South Africa.

Science for Life Laboratory, Drug Discovery & Development Platform and Division of Translational Medicine and Chemical Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.

出版信息

ChemistryOpen. 2025 Jul;14(7):e202400432. doi: 10.1002/open.202400432. Epub 2025 Jan 7.

Abstract

An efficient microwave-assisted synthesis route for novel oxazolidinone analogues has been developed. The general synthesis of these compounds began with an L-proline-mediated three-component Mannich reaction between commercially available 3-fluoro-4-morpholinoaniline, aqueous formaldehyde and α-hydroxyacetone. This was followed by a one-step cyclisation to form the core structure of oxazolidinone antibiotics which was subsequently derivatized. The novel compounds were evaluated for their antibacterial activity against M. smegmatis. One of the novel oxazolidinone derivatives 18 a1 produced a MIC of 8 mg/L, comparable with the commercial Rifampicin. The methodology is a useful addition to the field since it can make highly sought-after oxazolidinone derivatives, using cheaper, less harsh commercially available reagents, in a short time and one pot.

摘要

已开发出一种用于新型恶唑烷酮类似物的高效微波辅助合成路线。这些化合物的一般合成始于L-脯氨酸介导的市售3-氟-4-吗啉基苯胺、甲醛水溶液和α-羟基丙酮之间的三组分曼尼希反应。随后进行一步环化反应以形成恶唑烷酮抗生素的核心结构,该结构随后进行衍生化。评估了这些新型化合物对耻垢分枝杆菌的抗菌活性。新型恶唑烷酮衍生物之一18 a1的最低抑菌浓度为8 mg/L,与市售利福平相当。该方法是该领域的一项有益补充,因为它可以使用更便宜、腐蚀性更小的市售试剂,在短时间内一锅法制备出备受追捧的恶唑烷酮衍生物。

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