Synthesis and antioxidant activity of 2-methylthio-pyrido[3,2-e][1,2,4] triazolo[1,5-a]pyrimidines

被引:13
作者
Abuelizz, Hatem A. [1 ]
Taie, Hanan A. A. [2 ]
Marzouk, Mohamed [3 ]
Al-Salahi, Rashad [1 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11451, Saudi Arabia
[2] Natl Res Ctr, Dept Plant Biochem, Div Agr & Biol Res, 33 El Bohouth St, Giza 12622, Egypt
[3] Natl Res Ctr, Ctr Excellence Adv Sci, Chem Nat Prod Grp, 33 El Bohouth St, Cairo 12622, Egypt
来源
OPEN CHEMISTRY | 2019年 / 17卷 / 01期
关键词
pyrido-triazolopyrimidines; alkylation; thionation; antioxidants; DPPH; ANTIMICROBIAL ACTIVITY; DERIVATIVES;
D O I
10.1515/chem-2019-0092
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of 2-methylthio-pyrido-triazolopyrimidines (1-17) were prepared by the reaction of dimethyl-N-cyanoimidodithiocarbonate with hydrazinopyridine carboxylic acid as starting reactants. Their chemical structures were affirmed with HREI-MS, IR and NMR analyses. The target compounds (1-17) were evaluated for their antioxidant activity using 1,1-diphenyl-2-picryl hydrazyl (DPPH) radical scavenging, ferric reduction antioxidant power (FRAP) and reducing power capability (RPC). The results revealed that some pyrido-triazolopyrimidines showed good activity as antioxidant agents, in particular, compounds 12 and 15 were found to possess good antioxidant activity. Butylated hydroxyl toluene (BHT) was used as reference drug.
引用
收藏
页码:823 / 830
页数:8
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