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首页> 外文期刊>Asian journal of research in chemistry >Application of Chalcones in Synthesis of Novel 1, 5-Benzodiazepine Derivatives Containing Thieno [2,3-d] Pyrimidine Core Unit and its Biological Activity Screening
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Application of Chalcones in Synthesis of Novel 1, 5-Benzodiazepine Derivatives Containing Thieno [2,3-d] Pyrimidine Core Unit and its Biological Activity Screening

机译:Chalcons在含硫[2,3-D]嘧啶核心单元的新型1,5-苯二氮卓衍生物的应用及其生物活性筛选

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摘要

Di azepines, which were synthesized by different methods shown in literature and also Di azepines are great importance in heterocyclic chemistry and more importance in biology and pharmacology. Di azepines are very biological active molecules. In this work A new series of 1,5-Benzodizepine derivatives were synthesized from chalcones and evaluated for their Antimicrobial activities. First Chalcones were prepared by treatment of Thieno [2, 3-d] pyrimidine-6-carbaldehyde with different acetophenones by Claisen-Schimidt Condensation. Various Benzodiazepines derivatives were prepared by reaction of Chalcone in DMF with o-phenylene di amine in presence of piperidine. The structures of the newly synthesized Benzodiazepine derivatives have been established on the basis of their spectral data. The synthesized selected compounds were evaluated for their antimicrobial activities.
机译:通过文献中所示的不同方法合成的二氮杂豆类在杂环化学和对生物学和药理学中的重视方面具有重要意义。 DI ZZEPINE是非常生物的活性分子。 在这项工作中,新系列1,5-苯并嗪衍生物由Chalcone合成并评估其抗微生物活性。 首先通过Claisen-Schimidt缩合处理噻吩[2,3-D]嘧啶-6-咔啉,用不同的苯甲酮治疗噻吩[2,3-D]嘧啶-6-咔啉代表。 通过在哌啶存在下通过丙酮在DMF中的Chalcone在DMF中反应来制备各种苯二氮氧基喹啉衍生物。 新合成的苯并二氮卓衍生物的结构已经基于其光谱数据建立。 评价合成的选定化合物的抗微生物活性。

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