The Core‐Shell Magnetic Mesoporous Microspheres Immobilized NHC‐Palladacycles: An Efficient and Recyclable Catalyst for Suzuki‐Miyaura Cross‐Coupling of Pharmaceutical Synthesis
نویسندگان
چکیده
Abstract The core‐shell magnetic mesoporous microspheres immobilized NHC‐palladacycles (NHC= N ‐heterocyclic carbene) catalyst with constrained aliphatic linker group (Fe 3 O 4 @mSiO 2 @NHC−Pd) were readily prepared by the well‐designed method, which showed higher palladium loading (0.20 mmol g −1 ) and catalytic activity than non‐mesoporous catalysts @SiO same process in Suzuki‐Miyaura cross‐coupling reactions of aryl chlorides boronic acids. Herein, Fe @NHC−Pd could be used 12 times without significant loss, no leakage was detected both product residue, highlighting efficiency our strategy for immobilizing catalyst. Remarkably, this approach allows synthesis important drug intermediates 2‐aryl‐4‐aminoquinazolines o ‐tolylbenzonitrile (OTBN).
منابع مشابه
nano-rods zno as an efficient catalyst for the synthesis of chromene phosphonates, direct amidation and formylation of amines
چکیده ندارد.
Natural kaolin as an efficient recyclable catalyst for the synthesis of new 2,4-disubstituted quinolines
Substituted 2, 4- diphenyl quinolines were synthesized by a multicomponent domino reaction of anilines, aldehydes and terminal aryl alkynes. The synthetic pathway involves the formation of an imine, followed by the intermolecular addition of an alkyne to the imine. This intermediate immediately undergoes ring closure and oxidative aromatization. The reaction is catalyzed by natural kaolin, a st...
متن کاملNatural kaolin as an efficient recyclable catalyst for the synthesis of new 2,4-disubstituted quinolines
Substituted 2, 4- diphenyl quinolines were synthesized by a multicomponent domino reaction of anilines, aldehydes and terminal aryl alkynes. The synthetic pathway involves the formation of an imine, followed by the intermolecular addition of an alkyne to the imine. This intermediate immediately undergoes ring closure and oxidative aromatization. The reaction is catalyzed by natural kaolin, a st...
متن کاملBiFeO3 Magnetic Nanoparticles: A Novel, Efficient and Reusable Magnetic Catalyst for the Synthesis of Polyhydroquinoline Derivatives
Herein, it has been shown that the bismuth ferrite magnetic nanoparticles (BFO-MNPs) are new, efficient and recyclable catalysts for the synthesis of polyhydroquinoline derivatives by the Hantzsch reaction. The one-pot four-component cyclocondensation reaction of dimedone, aromatic aldehydes, ethyl acetoacetate and ammonium acetate was carried out under solvent-free conditions. The...
متن کامل-OSO3H Functionalized Mesoporous MCM-41 Coated on Fe3O4 Nanoparticles: an Efficient and Recyclable Nano-Catalyst for Preparation of 3,2′-Bisindoles
Mesoporous MCM-41 was coated on Fe3O4 nanoparticles and then functionalized with sulfurochloridic acid to provide a core-shell solid acid nano-catalyst. The catalyst was characterized by transmission electron microscopy (TEM), infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TG), Brunauer-Emmet-Teller analysis (BET) and vibrating sample magnetometery (VSM). The...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Asian Journal of Organic Chemistry
سال: 2022
ISSN: ['2193-5815', '2193-5807']
DOI: https://doi.org/10.1002/ajoc.202200018