Study on Synthesis, Spectral Characterization and in vitro Antibacterial Evaluation of Triaza and Dioxa Aza Spiro Derivatives

M. Natarajan, Elanchezhian Balachandravinayagam, S. Ganesan, M. Selvaraju
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Abstract

Six compounds 7,9-diphenyl-1,4-dioxa-8-azaspiro[4.5]decane 1-6 have been synthesized by Mannich reaction and cyclo condensation. The structures and stereochemistry established by Elemental analysis, Mass, IR, 1H,13C, NMR studies. The purities were checked by elemental analysis. The synthesized compounds 1-6 adopt chair conformation with equatorial orientation of the aryl groups by coupling constant values of 1H NMR. All the compounds were screened for their antibacterial activity against Proteus mirabilis, Klebsiella oxytoca, Staphylococcus aureus and Salmonella paratyphi. The compound 5 exhibited excellent in vitro antibacterial activity in all species.
Triaza和Dioxa Aza类螺旋衍生物的合成、光谱表征及体外抗菌评价研究
通过曼尼希反应和环缩合合成了6个化合物7,9-二苯基-1,4-二氧杂甲-8-氮杂螺[4.5]癸烷1-6。通过元素分析、质量、红外、1H、13C、核磁共振等方法确定了其结构和立体化学性质。通过元素分析检查了纯度。通过1H NMR偶联常数,合成的化合物1-6为芳基赤道取向的椅状构象。对所有化合物进行了对奇异变形杆菌、氧化克雷伯菌、金黄色葡萄球菌和副伤寒沙门氏菌的抑菌活性筛选。化合物5在所有物种中均表现出良好的体外抗菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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