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首页> 外文期刊>Asian journal of research in chemistry >Synthesis, Identification of Heterocyclic Compounds and Study of Biological Activity
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Synthesis, Identification of Heterocyclic Compounds and Study of Biological Activity

机译:杂环化合物的合成,鉴定及生物活性研究

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The aim of this work , synthesis of various hetero cycles (three, four, five, six, seven, and eight) -membered ring , containing one or more of hetero atoms as (N, S, O). This work involved five part , first part included synthesis of compounds (1-5) derived from cysteine when react with hydrazine , followed by electrophilic reactions to yield (aziridine ,diazhidine ,diazetidine, isoindole, diazine ) derivative . In second part ,the compound (6-14) was synthesized from reaction of phenylene diamine with carbondisulfide or glycine with phthalic anhydride to yield (thiazetidine,thiazepine, thiazolidine, diazirine.diazocin, benzimidazole, isoindole) derivatives .Third part, involved synthesis of triazole derivatives ( 17 ) from azotation of 1,3,4-thiadiazole to give (azo-imine ) compound (16) , followed by cyclization reaction. Four part involved synthesis of several hetero cycles from reaction of 1, 3,4-thiadiazole with sugars (xylose, arabinose, ribose), then reacted with (o-thiol benzoic, glycine, salicylic acid ) to produce the compounds (18-23). Five parts involved study of biological activity of some compounds. The structure of these compounds were characterized by (H.NMR ,FT.IR ,C.H.N) techniques ana their melting
机译:这项工作的目的是合成各种杂环(三个,四个,五个,六个,七个和八个),其中一个或多个杂原子为(N,S,O)。这项工作涉及五个部分,第一部分包括与肼反应时半胱氨酸衍生的化合物(1-5)的合成,然后进行亲电反应生成(氮丙啶,二氮杂,二氮杂啶,异吲哚,二嗪)衍生物。在第二部分中,由亚苯基二胺与二硫化碳或甘氨酸与邻苯二甲酸酐的反应合成了化合物(6-14),得到了(噻唑烷,噻氮平,噻唑烷,重氮嗪,重氮星,苯并咪唑,异吲哚)衍生物。将1,3,4-噻二唑偶氮化得到三唑衍生物(17),得到(偶氮-亚胺)化合物(16),然后环化反应。四个部分涉及从1,3,4-噻二唑与糖(木糖,阿拉伯糖,核糖)反应,然后与(邻硫醇苯甲酸,甘氨酸,水杨酸)反应生成化合物(18-23)合成几个杂环)。五个部分涉及某些化合物的生物活性研究。这些化合物的结构通过(H.NMR,FT.IR,C.H.N)技术进行了表征,并对其熔融进行了表征。

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