Heterocycles 39. Synthesis, characterization and evaluation of the anti-inflammatory activity of thiazolo[3,2-b][1,2,4]triazole derivatives bearing pyridin-3/4-yl moiety

被引:18
|
作者
Toma, Alexandra [1 ]
Mogosan, Cristina [2 ]
Vlase, Laurian [3 ]
Leonte, Denisa [1 ]
Zaharia, Valentin [1 ]
机构
[1] Iuliu Hatieganu Univ Med & Pharm, Dept Organ Chem, 41 Victor Babes St, RO-400012 Cluj Napoca, Romania
[2] Iuliu Hatieganu Univ Med & Pharm, Dept Pharmacol Physiol & Physiopathol, 6A L Pasteur St, RO-400349 Cluj Napoca, Romania
[3] Iuliu Hatieganu Univ Med & Pharm, Dept Pharmaceut Technol & Biopharmaceut, 12 I Creanga St, RO-400010 Cluj Napoca, Romania
关键词
Thiazolo[3,2-b][1,2,4]triazole; Pyridine; Antiinflammatory activity; BIOLOGICAL EVALUATION; PHARMACOLOGICAL EVALUATION; ANTIMICROBIAL ACTIVITY; RESISTANT BACTERIA; ANTICANCER AGENTS; THIAZOLES; INHIBITORS; ANALOGS; DESIGN;
D O I
10.1007/s00044-017-1959-x
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of pyridin-3/4-yl-thiazolo[3,2-b][1,2,4]triazole derivatives (5a-g, 6a-g) were synthesised by Hantzsch condensation of 5-pyridin-3/4-yl-1,2,4-triazole-3-thiol and diverse alpha-halocarbonyl compounds. Different reaction conditions (pH, temperature, solvent) were investigated for the efficient obtention of the target compounds. Under reflux and acidic conditions, the Hantzsch condensation was a one-step reaction. At room temperature and under basic conditions, it was possible to isolate the iminothioether intermediates 3/4a-g. These intermediates were cyclized in a subsequent step by treatment with concentrated sulphuric acid. The obtained compounds were evaluated for their anti-inflammatory activity. Three synthesised pyridyl-thiazolo[3,2-b][1,2,4]triazole derivatives (6c, 6d, 6f) were found to be good anti-inflammatory agents. [GRAPHICS] .
引用
收藏
页码:2602 / 2613
页数:12
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