Diversity Oriented Synthesis of 4H-Pyrimido[2,1-b]benzothiazole Derivatives via Biginellis Reaction: A Review

被引:13
|
作者
Gandhi, Divyani [1 ]
Kalal, Priyanka [1 ]
Prajapat, Prakash [1 ]
Agarwal, Dinesh Kumar [2 ]
Agarwal, Shikha [1 ]
机构
[1] Mohanlal Sukhadia Univ, Dept Chem, Synthet Organ Chem Lab, Udaipur 313001, Rajasthan, India
[2] PAHER Univ, Dept Pharmacol, Udaipur 313001, Rajasthan, India
关键词
2-Aminobenzothiazole; fused pyrimidobenzothiazole; Biginellis reaction; substituted benzaldehyde; 1,3-diketone; multicomponent one pot green synthesis; ONE-POT SYNTHESIS; ACIDIC IONIC LIQUID; MULTICOMPONENT SYNTHESIS; ANTIMICROBIAL ACTIVITY; PYRIMIDINE-DERIVATIVES; BIOLOGICAL EVALUATION; 3-COMPONENT REACTION; EFFICIENT SYNTHESIS; ANTITUMOR-ACTIVITY; FACILE SYNTHESIS;
D O I
10.2174/1386207321666180330170456
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Heterocycles have extended into widespread use for generating large collection of molecules in multi-component reactions. The development of new strategies for fused pyrimidobenzothiazole system has remained a highly attractive but challenging proposition for scientists working all around. Objective: The main objective of this work is to explore the utility of different catalysts as an ecofriendly reaction medium for green Biginellis reaction. Method: A detailed study of Biginellis reactions using various catalysts was done using different research tools. The methods involved reaction of equimolar mixture of benzothiazole, 1,3-diketone and aldehyde as reactants by conventional and greener pathways via Knoevenagal condensation. Results: The present review has several significant advantages for the scientists regarding green synthesis viz. green conditions, short reaction times, high yields, clean reaction conditions, easy isolation of products, simple work-up procedure and mild reaction conditions. Conclusion: Our report gives an overview of the combinatorial libraries for fused benzothiazole entities using metal catalyst, acid catalyst, ionic liquids, phase transfer catalyst, nano catalyst, etc.
引用
收藏
页码:236 / 253
页数:18
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