1245815-50-2

Upstream product

• 504-29-0 2-aminopyridine 
• 104-88-1 4-chlorobenzaldehyde 
• 536-74-3 phenylacetylene 
• 102990-14-7 1-(4-chlorophenyl)-3-phenylprop-2-yn-1-ol 
• 59045-98-6 N-(4-chlorobenzylidene)pyridin-2-amine 
• 637-44-5 phenylpropyolic acid 
• 7099-88-9 4-chlorophenylglyoxylic acid 

Relevant academic research and scientific papers

Magnetic Cu0@HAP@γ-Fe2O3 nanoparticles: An efficient catalyst for one-pot three-component reaction for the synthesis of imidazo[1,2-a]pyridines

Cu(0) incorporated magnetic hydroxyapatite nanoparticles (Cu0@HAP@γ-Fe2O3 NPs) was conveniently synthesized via the ion exchange reaction, oxidation, and reduction steps. The structure and composition of the nanohybrid wer

Magnetic nanostructure-anchored mixed-donor ligand system based on carboxamide and N-heterocyclic thiones: An efficient support of CuI catalyst for synthesis of imidazo[1,2-a]pyridines in eutectic medium

A Cu-incorporated nanocatalyst has been developed by immobilizing copper iodide on a magnetically retrievable mixed-donor ligand system, containing carboxamide, imidazolidine-2-thione and imidazole-2-thione donor groups and characterized by various analys

CuI/Fe3O4 NPs@Biimidazole IL-KCC-1 as a leach proof nanocatalyst for the synthesis of imidazo[1,2-a]pyridines in aqueous medium

In the present work, an innovative leach proof nanocatalyst based on dendritic fibrous nanosilica (DFNS) modified with ionic liquid loaded Fe3O4 NPs and CuI salts was designed and applied for the rapid synthesis of imidazo[1,2-a]pyri

Hydromagnesite sheets impregnated with cobalt-ferrite magnetic nanoparticles as heterogeneous catalytic system for the synthesis of imidazo[1,2-a]pyridine scaffolds

This paper manifests an A3-coupling strategy assisted by novel hydromagnesite sheets impregnated with cobalt ferrite (CoFe2O4-HMS) magnetic nanoparticles (MNPs) as an environmentally benign nanocomposite to synthesize imid

Copper Iodide Nanoparticles Immobolized Porous Polysulfonamide: An Effective Nanocatalyst for Synthesis of Imidazo [1,2-a] Pyridines

An efficient route was developed for the synthesis of a new polymer, porous cross-linked poly(ethyleneamine)-polysulfonamide (PEA-PSA), as an organic support for the imobilization of CuI nanoparticles (PEA-PSA@CuI). The resulting catalyst works as an effi

Development of novel efficient 2D nanocomposite catalyst towards the three-component coupling reaction for the synthesis of imidazo[1,2-a]pyridines

Two dimensional (2D) materials such as graphene and functionalized hexagonal boron nitride (h-BN) supported copper catalysts (CuO/rGO, CuO/h-BN, Cu(0)/rGO, Cu(0)/h-BN, CuS/rGO and CuS/h-BN) were prepared, characterized and evaluated their catalytic activity for the synthesis of imidazo[1,2-a]pyridines via one pot three component reaction between 2-aminopyridine, aldehyde and terminal alkynes. The imidazo[1,2-a]pyridines are an imperative class of nitrogen ring containing heterocyclic compounds which has wide range of applications in medicinal chemistry and drug molecule production. The reported synthetic protocol provides a rapid access to substituted imidazo[1,2-a]pyridines with excellent yields. CuO/rGO nanocomposite material was found to be highly active catalyst for the aforementioned reaction. The advantages of our protocol for the preparation of imidazo[1,2-a]pyridines over other previously reported includes shorter reaction times, functional group tolerance, recyclable catalyst and additive-free.

Facile synthesis of ZnAl2O4 nanoparticles: Efficient and reusable porous nano ZnAl2O4 and copper supported on ZnAl2O4 catalysts for one pot green synthesis of propargylamines and imidazo[1,

A simple, facile and efficient route was developed for the synthesis of nano ZnAl2O4 using ethanolamine. ZnAl2O4 nanoparticles were found to be smaller when calcined at 500 °C than at 700 °C. The synthesized nan

CuO-CuAl2O4 and d-glucose catalyzed synthesis of a family of excited state intramolecular proton transfer imidazo[1,2-a]pyridine analogues and their optical properties

A simple and efficient route to luminescent imidazo[1,2-a]pyridines from 2-aminopyridines, phenylacetylene and arylaldehydes was achieved by an one-pot, tandem process starting with an A3-coupling followed by 5-exo-dig cyclization. Copper(II)oxide/copper

Nano Fe3O4 supported biimidazole Cu(i) complex as a retrievable catalyst for the synthesis of imidazo[1,2-a]pyridines in aqueous medium

A novel magnetically recoverable nano-catalyst based on a biimidazole Cu(i) complex has been synthesized by covalent grafting of biimidazole on chloride-functionalized silica@magnetite nanoparticles, followed by metalation with CuI. The synthesized catalyst was characterized by various techniques such as CHN, NMR, FT-IR, TG/DTG, SEM, TEM, EDS, XRD, AAS, ICP-OES and VSM which revealed the superparamagnetic nature of the particles. The amount of Cu in the catalyst was measured to be 1.2 mmol g-1 by ICP-OES and AAS. From electron microscopy (SEM and TEM) studies it can be inferred that the particles are mostly spherical in shape and have an average size of 20 nm. Elemental and thermo gravimetric analysis (CHN and TG) results indicate the loading amount of functionalized organic groups on the magnetic material was 1.4 mmol g -1. The prepared nanocatalyst was shown to have excellent and green catalytic activity in the synthesis of imidazo[1,2-a]pyridines in aqueous media. The catalyst can be easily recovered by applying an external magnetic field and reused for atleast 10 times without deterioration in catalytic activity.

Synthesis of Imidazo[1,2-a]pyridines using fe3o 4@sio2 as an efficient Nanomagnetic catalyst via a one-pot Multicomponent reaction

A one-pot multicomponent synthesis of imidazo[1,2-a]pyridine derivatives by using pyridin-2-amines, aldehydes, and terminal alkynes in the presence of a catalytic amount of silica-supported iron oxide (Fe3O 4@SiO2) nanopar