401466-91-9

Upstream product

• 118-48-9 isatoic anhydride 
• 519-05-1 opianic acid 
• 100-46-9 benzylamine 
• 52745-10-5 N-(phenylmethyl)-2-nitrobenzamide 

Relevant academic research and scientific papers

Synthesis of isoindolo[2,1-a]quinazoline-5,11-dione derivatives via the reductive one-pot reaction of N-substituted 2-nitrobenzamides and 2-formylbenzoic acids

Various isoindolo[2,1-a]quinazoline-5,11-dione derivatives 3 were synthesized in good yields by means of the reductive reaction of N-substituted 2-nitrobenzamides 1 and 2-formylbenzoic acids 2 in the presence of SnCl 2·2 H2O under reflux in EtOH (Scheme, Table). The procedure needed two steps, the reduction of the nitro group of the 2-nitrobenzamide and ring closure by nucleophilic addition of the NH2 group to both the formyl and carboxylic acid C=O groups. Copyright

The synthesis of 2,3-dihydroquinazoline-4(1H)-one and dihydroisoindolo[2,1-a]quinazoline-5,11-dione derivatives in the presence of imidazolium ionic liquid sulfonic acid functionalized SBA-15: A novel feature of SBA-15

Imidazole-based ionic liquid-supported on SBA-15 (ImIL-Sul-SBA-15) as a novel heterogeneous catalyst was designed, synthesized and characterized by FT-IR, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET) analysis. This novel nano structure was used for the synthesis of various 2,3-dihydroquinazoline-4(1H)-one and dihydroisoindolo[2,1-A]quinazoline-5,11-dione derivatives via three-component reaction between isatoic anhydride, amines and aromatic aldehydes at 50 °C in ethanol and water mixture as solvent. We found the synthetic imidazolium ionic liquid sulfonic acid functionalized SBA-15 as a convenient catalyst for this methodology. The catalyst performs the reaction in mild reaction conditions, and can easily be separated from the reaction mixture by simple filtration, with no need to tedious purification steps. Formula parented.