Contemporary progress in the synthesis and reactions of 2-aminobenzothiazole: a review

被引:61
作者
Dadmal, Tulshiram L. [1 ,2 ]
Katre, Sangita D. [3 ]
Mandewale, Mustapha C. [1 ]
Kumbhare, Ravindra M. [2 ]
机构
[1] Govt Maharashtras, Ismail Yusuf Coll, Dept Chem, Bombay 400060, Maharashtra, India
[2] Indian Inst Chem Technol, Fluoroorgan Div, Hyderabad 500607, Andhra Prades, India
[3] Chhotabhai Javerbhai Patel Coll, Dept Chem, Tirora 441911, Gondia, India
关键词
ONE-POT SYNTHESIS; COPPER-CATALYZED SYNTHESIS; METAL-FREE SYNTHESIS; OXIDATIVE C-H; BIOLOGICAL EVALUATION; UREA DERIVATIVES; DIRECT AMINATION; BENZOTHIAZOLES; INHIBITORS; EFFICIENT;
D O I
10.1039/c7nj03776g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the past few decades, heterocyclic compounds and their derivatives have gained popularity due to their prominent medicinal importance. The versatile and synthetically accessible 2-aminobenzothiazole scaffolds are quite fascinating for multiple applications in both synthetic organic chemistry and biological fields due to their potent pharmacological activities. A large number of efforts have been made to develop a wide range of methodologies for the synthesis of 2-aminobenzothiazole and its derivatives. Moreover, 2-aminobenzothiazole significantly serves as a reactant or a reaction intermediate for affording various fused heterocycles since NH2 and endocyclic N functions of 2-aminobenzothiazole are suitable to assist reactions with common bis electrophilic reagents to form a diverse fused heterocyclic scaffold. This review highlights various synthetic methodologies and chemical reactions of 2-aminobenzothiazole.
引用
收藏
页码:776 / 797
页数:22
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