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A “One Pot,” Environmentally Friendly, Multicomponent Synthesis of 2‐Amino‐5‐cyano‐4‐[(2‐aryl)‐1 H ‐indol‐3‐yl]‐6‐hydroxypyrimidines and Their Antimicrobial Activity
Author(s) -
Gupta Ragini,
Jain Anshu,
Madan Yogita,
Menghani Ekta
Publication year - 2014
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.1796
Subject(s) - chemistry , aspergillus flavus , fusarium oxysporum , antimicrobial , aryl , carbon 13 nmr , proton nmr , guanidine , antibacterial activity , organic chemistry , nuclear chemistry , yield (engineering) , bacteria , food science , botany , alkyl , genetics , materials science , metallurgy , biology
A series of multifunctional 2‐amino‐5‐cyano‐4‐[(2‐aryl)‐1 H ‐indol‐3‐yl]‐6‐hydroxypyrimidines ( 4a , 4b , 4c , 4d , 4e , 4f ) was synthesized by multicomponent reaction of 3‐formylindole ( 1 ), cyanoethylacetate ( 2 ), and guanidine hydrochloride ( 3 ) with NaOH by using green chemical techniques, viz. microwave irradiation and grindstone technology. The same reactants when refluxed in ethanol also gave titled compounds ( 4a , 4b , 4c , 4d , 4e , 4f ). Compared with conventional procedure, the reaction can be carried out under milder conditions, requiring a shorter reaction time and giving higher yields following the green chemistry methodology. All the synthesized compounds have been characterized on the basis of elemental analyses and spectral data (IR, 1 H NMR, 13 C NMR, and mass). All synthesized compounds were also evaluated for their antimicrobial activity against nine pathogenic bacteria, antifungal activity against Rhizopus stolonifer , Aspergillus flavus , and Fusarium oxysporum and antibacterial activity against Escherichia coli and Pseudomonas aeruginosa at different concentrations. Most of the compounds showed mild to moderate activity.