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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SYNTHESIS, CRYSTAL STRUCTURE AND ANTIBACTERIAL EVALUATION OF N-SUBSTITUTED PERHYDRO-1,3-OXAZIN-2-ONES CONTAINING N-PHENYLSULFONAMIDE
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SYNTHESIS, CRYSTAL STRUCTURE AND ANTIBACTERIAL EVALUATION OF N-SUBSTITUTED PERHYDRO-1,3-OXAZIN-2-ONES CONTAINING N-PHENYLSULFONAMIDE

机译:含N-苯磺酰胺的N-取代的-1,3-恶嗪-2-酮的合成,晶体结构和抗菌评估

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摘要

The synthesis of a new series of N-substituted perhydro-1,3-oxazin-2-ones containing N-phenylsulfonamide is described. The compounds 7a-7f were obtained in a one-pot reaction from chlorosulfonyl isocyanate, selected 1,3-halogenoalcohols and various aromatic amines in alkaline conditions, to give the target N-heterocyclic 6-membered ring compounds with good yields. The X-ray crystal structure of N-[(N-4-fluorophenyl)sulfamoyl]perhydro-1,3-oxazin-2-one 7d was solved. All the synthesized compounds have been screened for their in-vitro antibacterial activity against Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa. Structures of 7d and 6e can be further optimized to give new potent antibacterial agents with structures significantly different from those of existing classes of antibiotics.
机译:描述了含有N-苯基磺酰胺的一系列新的N-取代的全氢-1,3-恶嗪-2-酮的合成。在碱性条件下,通过一锅反应从异氰酸氯磺酰基酯,选择的1,3-卤代醇和各种芳香胺获得化合物7a-7f,从而以良好的收率得到目标N-杂环6元环化合物。解析了N-[(N-4-氟苯基)氨磺酰基]过氢-1,3-恶嗪-2-酮7d的X射线晶体结构。已经筛选了所有合成的化合物对金黄色葡萄球菌,大肠杆菌和铜绿假单胞菌的体外抗菌活性。可以进一步优化7d和6e的结构,以提供新的有效抗菌剂,其结构与现有抗生素类别明显不同。

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