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Immobilized Ni on TMEDA@ßSiO2@αSiO2@Fe3O4: as a novel magnetic nanocatalyst for preparation of pyrido[2,3-d:6,5-d']dipyrimidines.
Almajidi, Yasir Qasim; Ubaidullah, Mohd; Pandit, Bidhan; Kareem, A K; Romero-Parra, Rosario Mireya; Bobirjon, Adizov; Kadhum, Wesam R; Al-Erjan, Amran M; Abosaooda, Munther; Mahmoud, Aisha Kamal.
  • Almajidi YQ; Department of Pharmacy (Pharmaceutics), Baghdad College of Medical Sciences Baghdad Iraq.
  • Ubaidullah M; Department of Chemistry, College of Science, King Saud University P.O. Box 2455 Riyadh 11451 Saudi Arabia mtayyab@ksu.edu.sa mohdubaidullah2007@gmail.com.
  • Pandit B; Department of Materials Science and Engineering and Chemical Engineering, Universidad Carlos III de Madrid, Avenida de la Universidad 30 28911 Leganés Madrid Spain.
  • Kareem AK; Biomedical Engineering Department, Al-Mustaqbal University College 51001, Hillah Iraq.
  • Romero-Parra RM; Department of General Studies, Universidad Continental Lima Peru.
  • Bobirjon A; Chief Researcher of the Institute of General and Inorganic Chemistry, Academy of Sciences of the Republic of Uzbekistan Mirzo Ulugbek avenue 77A 100071 Uzbekistan Tashkent.
  • Kadhum WR; Department of Pharmacy, Kut University College Kut 52001 Wasit Iraq.
  • Al-Erjan AM; Department of Anesthesia, College of Health & Medical Technology, Al-Ayen University Thi-Qar Iraq.
  • Abosaooda M; College of Pharmacy, The Islamic University 54001 Najaf Iraq.
  • Mahmoud AK; Al-Nisour University College Baghdad Iraq.
RSC Adv ; 13(17): 11393-11405, 2023 Apr 11.
Article en En | MEDLINE | ID: mdl-37063709
ABSTRACT
In the current body of research, a very quick and effectual procedure for the synthesis of pyrido[2,3-d6,5-d']dipyrimidines has been developed. This method is accomplished through the one-pot multi-component reaction of 2-thiobarbituric acid, NH4OAc and aldehydes utilizing Ni-TMEDA@ßSiO2@αSiO2@Fe3O4 as a novel mesoporous nanomagnetic catalyst at room temperature. This protocol is one of the few reports of the preparation of these derivatives without the use of conventional heating as well as energies such as microwave and ultrasound radiation. The characterization of the prepared catalyst was well accomplished by different techniques such as FT-IR, ICP-OES, SEM, TEM, BET, XRD, VSM, TGA, EDX and Elemental mapping. This organometallic catalyst was reusable for seven times with negligible decrement in its catalytic performance. In addition, all of the products were produced with high TON and TOF values, which demonstrates that our catalyst has a very high level of activity in the preparation of pyrido[2,3-d6,5-d']dipyrimidines.