One Pot Multicomponent Synthesis of Highly Commutated 1,2,3-Triazoles using some Pyrazole aldehyde through "Click" Reaction

被引:1
|
作者
VETRISELVAN, M. O. O. R. T. H. Y. [1 ]
PRAMESH, M. A. N. I. C. K. A. M. [1 ]
JAYANTHI, S. E. L. V. A. R. A. J. [1 ]
GUNASUNDARI, K. I. T. T. A. P. P. A. [1 ]
SHANMUGAM, P. O. N. N. U. S. A. M. Y. [2 ]
机构
[1] AVVM Sri Pushpam Coll, PG & Res Dept Chem, Poondi 613503, Tamil Nadu, India
[2] CSIR Cent Leather Res Inst CLRI, Organ & Bioorgan Chem Div, Chennai 60020, Tamil Nadu, India
关键词
1,2,3-triazole; Pyrazole aldehyde; Click reaction; CuAAC; AZIDE-ALKYNE CYCLOADDITION; RUTHENIUM-CATALYZED CYCLOADDITION; CHEMISTRY; THERAPY;
D O I
10.13005/ojc/380209
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
1,2,3 Trizole compounds are widely applied in major several technical and research areas especially in drug discovery new chemical entities like trizoles are developed via click reactions. Synthesis of heterocycles through cycloaddition reaction between azides and alkynes by employing and azides using copper as catalyst is said to be Click reaction. Most commonly triazoles are utilized in medicinal field as a drug linkers for bioconjugation. It found to have potential multiple applications in biological as well as medical sciences. We describe herein the novel and efficient three step multicomponent synthesis of highly substituted 1,2,3-triazole derivatives from pyrazole aldehyde, diaminobenzene via N-alkylation by Click reaction. For the future, our perspective is studies of anti-cancer, anti-viral and antimicrobial activities in 1,2,3-triazole.
引用
收藏
页码:295 / 301
页数:7
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