TY - JOUR
T1 - Metal-doped TiO2nanocatalysts in an MX2/urea mixture for the synthesis of benzothiazoles bearing substituted pyrrolidin-2-ones
T2 - Enhanced catalytic performance and antibacterial activity
AU - Geesi, Mohammed H.
AU - Ouerghi, Oussama
AU - Dehbi, Oussama
AU - Riadi, Yassine
N1 - Publisher Copyright:
© 2021 Elsevier Ltd.
PY - 2021/8
Y1 - 2021/8
N2 - Solvents and catalysts are among the key factors in achieving the green chemical synthesis of bioactive compounds. In this regard, metal-doped nanoparticles, as a heterogeneous catalyst, in urea-based deep eutectic mixtures were used to prepare a series of pyrrolidinone-substituted benzothiazoles. In the strategy developed herein, pyrrolidinone derivatives were synthesized by reacting different arylamines with dimethyl itaconate using water as the solvent in a microwave. Then, the as-obtained pyrrolidinone derivatives were reacted with 2-aminothiophenol under microwave irradiation with the assistance of a deep eutectic mixture (CuCl2 or NiCl2/urea) and Cu- or Ni-doped TiO2 nanoparticles to afford the final derivative incorporating both pyrrolidin-2-one and benzothiazole rings. To determine the optimum reaction conditions, the effect of temperature, solvent nature, and reaction time was investigated. Under the optimal operation conditions, high reaction yields were achieved. The developed strategy exhibited advantages of a short reaction time, eco-friendliness, and high productivity. Finally, the obtained derivatives were examined in terms of their antibacterial potential against selected Gram-negative and Gram-positive bacterial strains: Eight of the derivatives exhibited activity against the tested bacteria.
AB - Solvents and catalysts are among the key factors in achieving the green chemical synthesis of bioactive compounds. In this regard, metal-doped nanoparticles, as a heterogeneous catalyst, in urea-based deep eutectic mixtures were used to prepare a series of pyrrolidinone-substituted benzothiazoles. In the strategy developed herein, pyrrolidinone derivatives were synthesized by reacting different arylamines with dimethyl itaconate using water as the solvent in a microwave. Then, the as-obtained pyrrolidinone derivatives were reacted with 2-aminothiophenol under microwave irradiation with the assistance of a deep eutectic mixture (CuCl2 or NiCl2/urea) and Cu- or Ni-doped TiO2 nanoparticles to afford the final derivative incorporating both pyrrolidin-2-one and benzothiazole rings. To determine the optimum reaction conditions, the effect of temperature, solvent nature, and reaction time was investigated. Under the optimal operation conditions, high reaction yields were achieved. The developed strategy exhibited advantages of a short reaction time, eco-friendliness, and high productivity. Finally, the obtained derivatives were examined in terms of their antibacterial potential against selected Gram-negative and Gram-positive bacterial strains: Eight of the derivatives exhibited activity against the tested bacteria.
KW - Antibacterial
KW - Arylamines
KW - Benzothiazole
KW - Metal-doped TiOnanocatalyst
KW - Pyrrolidin-2-one
KW - Urea-based DESs
UR - http://www.scopus.com/inward/record.url?scp=85102891515&partnerID=8YFLogxK
U2 - 10.1016/j.jece.2021.105344
DO - 10.1016/j.jece.2021.105344
M3 - Article
AN - SCOPUS:85102891515
SN - 2213-2929
VL - 9
JO - Journal of Environmental Chemical Engineering
JF - Journal of Environmental Chemical Engineering
IS - 4
M1 - 105344
ER -