Facile synthesis, characterization and pharmacological activities of 3,6-disubstituted 1,2,4-triazolo[3,4-b][1,3,4]thiadiazoles and 5,6-dihydro-3,6-disubstituted-1,2,4-triazolo[3,4-b][1,3,4]thiadiazoles

被引:44
作者
Chidananda, N. [1 ,2 ]
Poojary, Boja [1 ]
Sumangala, V. [1 ,2 ]
Kumari, N. Suchetha [3 ]
Shetty, Prashanth [4 ]
Arulmoli, T. [2 ]
机构
[1] Mangalore Univ, Dept Studies Chem, Mangalagangothri 574199, Karnataka, India
[2] SeQuent Sci Ltd, Ind Area, New Mangalore 575011, Karnataka, India
[3] KS Hegde Med Acad, Dept Biochem, Deralakatte 574162, Karnataka, India
[4] NGSM Inst Pharmaceut Sci, Mangalore 574160, Karnataka, India
关键词
Triazoles; Triazolo[3,4-b][1,3,4]thiadiazoles; Anti-inflammatory activity; Analgesic activity; Antioxidant activity; Anti-microbial activities; HETEROCYCLIC SYSTEM; 1,2,4-TRIAZOLO;
D O I
10.1016/j.ejmech.2012.02.030
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Two new series of compounds namely, 3,6-disubstituted-1,2,4-triazolo[3,4-b][1,3,4]thiadizoles (5a-j) and 5,6-dihydro-3,6-disubstituted-1,2,4-triazolo[3,4-b][1,3,4]thiadizoles (7a-j) were prepared. In continuation of a previously reported study, the first series (5a-j) were synthesized by the cyclo-condensation of 4-amino-5-(2-bromo-5-methoxyphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (4) with various substituted aromatic carboxylic acids in phosphorus oxychloride and the second series (7a-j) by the reaction of (4) with various substituted aromatic aldehydes in the presence of p-Toluene sulfonic acid. Reaction of (4) with the aldehyde (9) afforded the Schiff's base (10) and not the cyclised product (11) on treatment with p-Toluene sulfonic acid. Synthesized compounds were structurally confirmed by spectral analysis and studied for their anti-inflammatory, analgesic, anti-oxidant and antimicrobial activities. Some of the tested compounds showed significant pharmacological activities. (C) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:124 / 136
页数:13
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