scholarly journals Simple, novel, and efficient synthesis of ethyl 2-(2-(1H-indol-3-yl)benzo[d]thiazol-3(2H)-yl)-2-cyanoacetate or acetate via a three-component reaction

2020 ◽  
pp. 174751982095201
Author(s):  
Mahmoud Nassiri ◽  
Forough Jalili Milani

Ethyl 2-(2-(1 H-indol-3-yl)benzo[ d]thiazol-3(2 H)-yl)-2-cyanoacetate or acetate 6a–f as a series of novel compounds were synthesized from the reactions of benzothiazole, 2-methylbenzothiazole, or 2,5-dimethylbenzothiazole and ethyl bromocyanoacetate with indole derivatives. The reactions proceeded in acetone as a solvent under reflux for 5 h in good yields. The structures of new compounds were confirmed by 1H nuclear magnetic resonance, 13C nuclear magnetic resonance, infrared, elemental analyses, and mass spectroscopy.

2020 ◽  
pp. 174751982093990
Author(s):  
Yuting Liu ◽  
Lan Yang ◽  
Dawei Yin

Ferrocenyl imidazolo[2,1- b]-1,3,4-thiadiazoles are synthesized using 2-amino-5-substituted-1,3,4-thiadiazole and α-bromoacetyl ferrocene as substrates under microwave-assisted and catalyst-free conditions. The structures are characterized by infrared, 1H nuclear magnetic resonance, 13C nuclear magnetic resonance, mass spectrometry, and elemental analysis. Compared with conventional methods, the present protocol has the advantages of being rapid, efficient, environmentally friendly, and low cost. The results of biological activity studies showed that the products displayed better activities than those of 2-amino-5-substituted-1,3,4-thiadiazole. The biological activities of compounds in which R = phenyl were better than those with alkyl groups. Compounds with electron-withdrawing groups on the aryl moiety showed increased biological activities.


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