Synthesis and Antitubercular Activity of Novel 1,3,4-Oxadiazole and 1,3,4-Thiadiazole Derivatives

被引:0
|
作者
Joshi, Shrinivas D. [1 ]
Tiwari, Sahilkumar [1 ]
Kulkarni, Venkatarao H. [1 ]
机构
[1] Soniya Educ Trusts, Coll Pharm, Dept Pharmaceut Chem, Novel Drug Design & Discovery Lab, Dharwad, Karnataka, India
关键词
Oxadiazoles; Thiadiazoles; 2-(1H-Benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate; N'; N'-Diisopropylethylamine; N'-Dimethyl formamide; Mycobacterium tuberculosis H(37)Rv; Antitubercular activity; ACID HYDRAZIDE ANALOGS; PYRROLE RING-SYSTEMS; ANTIMYCOBACTERIAL AGENTS; POTENTIAL ANTIBACTERIAL; INHIBITORS; OXADIAZOLE; TRIAZOLE;
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Oxadiazole pyrrolyl benzamide derivatives (4a-e) and thiadiazole pyrrolyl benzamide derivatives (5a-e) were synthesized by the reaction of 4-(1H-pyrrol-1-yl) benzoic acid with N-(5-(4substituted phenyl)-1,3,4-oxadiazole-2-amines and N-(5-(4-substituted phenyl)-1,3,4-thiadiazole-2-amines, respectively, in N', N'-dimethyl formamide using 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate as amide coupling agent and N', N'-Diisopropylethylamine as a catalyst. All the newly synthesized compounds (4a-e/5a-e) were screened for in vitro antitubercular activity against Mycobacterium tuberculosis H(37)Rv, and compounds 4c, 4d, 5c, and 5d have exhibited significant minimum inhibitory concentration values.
引用
收藏
页码:417 / 421
页数:5
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