52537-82-3Relevant academic research and scientific papers
Synthesis of quinazolines over recyclable Fe3O4@SiO2-PrNH2-Fe3+ nanoparticles: A green, efficient, and solvent-free protocol
Eidi, Esmaiel,Kassaee, Mohamad Z.,Nasresfahani, Zahra,Cummings, Peter T.
, (2018/09/25)
A practical and efficient method is developed for efficient synthesis of quinazoline derivatives through condensation reaction of 2-aminoaryl ketone, an aldehyde, and ammonium acetate, over magnetic Fe3O4@SiO2-PrNH2/
A new and facile CuCl2·2H2O-catalyzed one-pot three-component synthesis for quinazolines
Saad, Syed Muhammad,Khan, Khalid Mohammed,Perveen, Shahnaz,Voelter, Wolfgang,Taha, Muhammad
, p. 1877 - 1880 (2015/10/29)
A new and facile CuCl2·2H2O-catalyzed one-pot three-component synthesis for quinazolines has been developed. A mixture of readily available 2-amino-5-chlorobenzophenones, substituted benzaldehydes, ammonium acetate, and CuCl2/s
Recyclable, magnetic ionic liquid bmim[FeCl4]-catalyzed, multicomponent, solvent-free, green synthesis of quinazolines
Panja, Sumit Kumar,Saha, Satyen
, p. 14495 - 14500 (2013/09/02)
An atom-efficient, eco-friendly, solvent-free, high yielding, multicomponent green strategy to synthesize highly functionalized quinazoline derivatives by the one-pot reaction of 2-aminobenzophenone, aromatic aldehyde and ammonium acetate is presented. Ma
Catalyst-free synthesis of quinazoline derivatives using low melting sugar-urea-salt mixture as a solvent
Zhang, Zhan-Hui,Zhang, Xiao-Nan,Mo, Li-Ping,Li, Yong-Xiao,Ma, Fei-Ping
experimental part, p. 1502 - 1506 (2012/06/04)
Low melting mixture of maltose-dimethylurea (DMU)-NH4Cl was found to be an inexpensive, non-toxic, easily biodegradable and effective reaction medium in the catalyst-free synthesis of quinazoline derivatives. This simple and efficient method fu
Ecofriendly and efficient one-pot procedure for the synthesis of quinazoline derivatives catalyzed by an acidic ionic liquid under aerobic oxidation conditions
Dabiri, Minoo,Salehi, Peyman,Bahramnejad, Mahboobeh
experimental part, p. 3214 - 3225 (2010/12/24)
A three-component condensation reaction between 2-aminobenzophenone derivatives, formaldehyde or aromatic aldehydes, and ammonium acetate efficiently provides substituted quinazolines in a one-pot reaction in the presence of Bronsted acidic ionic liquid, 1-methylimidazolium triflouroacetate ([Hmim]TFA), in conjunction with aerobic oxidation. The ionic liquid was separated from the reaction mixture by simple extraction and was recycled three times without considerable loss in activity. Copyright Taylor & Francis Group, LLC.
