首页> 外文期刊>Journal of Chemistry >Synthesis and Bioactivity of Some New 3-Alkyl-2,4-diisopropyl-1,2,4,5-tetrahydro-benzo[e][1,3,2]-diazaphosphepine 3-sulfides/selenides
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Synthesis and Bioactivity of Some New 3-Alkyl-2,4-diisopropyl-1,2,4,5-tetrahydro-benzo[e][1,3,2]-diazaphosphepine 3-sulfides/selenides

机译:一些新的3-烷基-2,4-二异丙基-1,2,4,5-四氢苯并[e] [1,3,2] - 二氧化亚甲基3-硫化物/硒化物的合成及生物活性

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Preparation of a series of novel seven membered heterocyclic compounds, 3-alkyl-2,4-diisopropyl-1,2,4,5-tetrahydro-benzo[e][1,3,2] diazaphosphepine 3-sulfides / selenides (8a-l) was accomplished in four steps. The synthetic route involves α,α′-dibromo-o-xylene (1) with two moles of isopropylamine (2) in the presence of triethylamine (TEA) in dry tetrahydrofuran (THF) at low temperature to form the compound3. This on treatment with phosphorus tribromide (4) in the presence of TEA in dry THF to form the corresponding phosphorobromodite (5). This on subsequent reaction with different Grignard reagents (6) in dry THF under N2atmosphere formed the compounds7. They are converted to the corresponding sulfides and selenides (8a-l) by reacting them with sulfur and selenium respectively. Their structures were established by elemental analysis, IR,1H,13C,31P NMR and mass spectral data. All the title compounds were screened for theirantibacterial activity. Most of the compounds exhibited significant antimicrobial activity.
机译:制备一系列新型七元杂环化合物,3-烷基-2,4-二异丙基-1,2,4,5-四氢 - 苯并[e] [1,3,2]二硫化物/硒化物(8A -L)是以四个步骤完成的。合成途径涉及α,α'-dibromo-O-二甲苯(1),其在低温下在干燥四氢呋喃(THF)中的三乙胺(THF)存在下具有两摩尔异丙胺(2)以形成化合物3。在干燥THF的茶叶存在下,用磷三溴化物(4)处理以形成相应的磷罗马霉(5)。在N 2液晶下的干燥THF中与不同格子试剂(6)的随后反应形成化合物7。它们通过分别用硫和硒反应而转化为相应的硫化物和硒化酯(8a-L)。它们的结构是由元素分析,IR,1H,13C,31P NMR和质谱数据建立的。筛选所有标题化合物以进行分散杆菌活性。大多数化合物表现出显着的抗微生物活性。

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