{"title":"类似哌嗪的三唑类化合物的合成及生物活性研究","authors":"A. Nagaraj, S. Srinivas, G. N. Rao","doi":"10.29055/JCCS/684","DOIUrl":null,"url":null,"abstract":"A new series of novel (5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)(4arylpiperazino)methanone 8(a-j) has been synthesized from 5-methyl-1-phenyl-1H1,2,3-triazole-4-carboxylic acid 4 and 1-arylpiperazine 7(a-j). Chemical structures of all the new compounds were established by IR, H, C NMR and MS data. The compounds 8(a-j) were evaluated for their antibacterial activity against four human pathogenic bacteria viz., Escherichia coli, Klebseilla pneumoniae, Shigella dysentriae and Shigella flexnei. Amongst them, compounds having 4-methylphenyl 8b, 4-methoxyphenyl 8c, 4-fluorophenyl 8d, 4-bromophenyl 8e and 3-nitrophenyl 8f moieties on piperazine ring showed significant inhibition of bacterial growth and emerged as potential molecules for further development.","PeriodicalId":15337,"journal":{"name":"Journal of Chemistry and Chemical Sciences","volume":"70 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Synthesis and Biological Activity of Triazole Analogues\\nof Piperazine\",\"authors\":\"A. Nagaraj, S. Srinivas, G. N. Rao\",\"doi\":\"10.29055/JCCS/684\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A new series of novel (5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)(4arylpiperazino)methanone 8(a-j) has been synthesized from 5-methyl-1-phenyl-1H1,2,3-triazole-4-carboxylic acid 4 and 1-arylpiperazine 7(a-j). Chemical structures of all the new compounds were established by IR, H, C NMR and MS data. The compounds 8(a-j) were evaluated for their antibacterial activity against four human pathogenic bacteria viz., Escherichia coli, Klebseilla pneumoniae, Shigella dysentriae and Shigella flexnei. Amongst them, compounds having 4-methylphenyl 8b, 4-methoxyphenyl 8c, 4-fluorophenyl 8d, 4-bromophenyl 8e and 3-nitrophenyl 8f moieties on piperazine ring showed significant inhibition of bacterial growth and emerged as potential molecules for further development.\",\"PeriodicalId\":15337,\"journal\":{\"name\":\"Journal of Chemistry and Chemical Sciences\",\"volume\":\"70 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemistry and Chemical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.29055/JCCS/684\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemistry and Chemical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29055/JCCS/684","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis and Biological Activity of Triazole Analogues
of Piperazine
A new series of novel (5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)(4arylpiperazino)methanone 8(a-j) has been synthesized from 5-methyl-1-phenyl-1H1,2,3-triazole-4-carboxylic acid 4 and 1-arylpiperazine 7(a-j). Chemical structures of all the new compounds were established by IR, H, C NMR and MS data. The compounds 8(a-j) were evaluated for their antibacterial activity against four human pathogenic bacteria viz., Escherichia coli, Klebseilla pneumoniae, Shigella dysentriae and Shigella flexnei. Amongst them, compounds having 4-methylphenyl 8b, 4-methoxyphenyl 8c, 4-fluorophenyl 8d, 4-bromophenyl 8e and 3-nitrophenyl 8f moieties on piperazine ring showed significant inhibition of bacterial growth and emerged as potential molecules for further development.