74375-35-2Relevant academic research and scientific papers
Eco-friendly and efficient synthesis of 2,3-dihydroquinazolin-4(1H)-ones
Majid, Ghashang,Kobra, Azizi,Hamed, Moulavi-Pordanjani,Hamid Reza, Shaterian
, p. 1617 - 1623 (2011)
A simple and facile method for the synthesis of 2,3-dihydroquinazolin-4(1H) -ones through the direct cyclocondensation of one-pot three-component cyclocondensation of isatoic anhydride, ammonium acetate (or primary amines) and aldehydes; and anthranilamide and aldehydes using silica supported ferric chloride (SiO2-FeCl3) as catalyst under solvent-free conditions is described.
One-pot synthesis of 2,3-dihydroquinazolin-4(1H)-ones by Fe3O4@SiO2-imid-PMAn nano-catalyst under ultrasonic irradiation and reflux conditions
Esmaeilpour, Mohsen,Javidi, Jaber,Zahmatkesh, Saeed,Fahimi, Nafiseh
, p. 947 - 956 (2017/04/14)
Abstract: Fe3O4@SiO2-imid-PMAn efficiently catalyzes the condensation reaction of isatoic anhydride, aldehydes, and primary amines or ammonium salts to afford the corresponding 2,3-dihydroquinazolin-4(1H)-one derivatives under ultrasonic irradiation or reflux conditions. This method gives notable advantages such as operational simplicity, excellent yields, short reaction times, and absence of any tedious workup or purification. In addition, the excellent catalytic performance and the easy preparation, thermal stability, and separation of the catalyst make it a good heterogeneous system and a useful alternative to other heterogeneous catalysts. Also, the aforementioned nanocatalyst can be easily recovered by a magnetic field and reused for subsequent reactions for at least six times without noticeable deterioration in catalytic activity and reaction yield. Graphical abstract: [Figure not available: see fulltext.]
Br?nsted acidic ionic liquids catalyze the preparation of 2,3-dihydroquinazolin-4(1H)-one derivatives
Shaterian, Hamid Reza,Aghakhanizadeh, Morteza
, p. 1655 - 1668 (2014/05/06)
A simple and facile method for the green synthesis of 2,3- dihydroquinazolin-4(1H)-one derivatives by direct three-component cyclo-condensation of isatoic anhydride, ammonium acetate (or primary amines), and arylaldehydes using different Br?nsted acidic ionic liquids, for example 2-pyrrolidonium hydrogensulfate ([hnmp][HSO4]), N-methyl-2-pyrrolidonium hydrogensulfate ([NMP][HSO4]), and N-methyl-2-pyrrolidonium dihydrogenphosphate ([NMP][H2PO 4]), as reusable catalysts under solvent-free conditions is described. In addition, reaction of anthranilamide and arylaldehydes for synthesis of 2,3-dihydroquinazolin-4(1H)-one derivatives was investigated.
Efficient synthesis of mono- and disubstituted 2,3-dihydroquinazolin-4(1H)- ones using copper benzenesulfonate as a reusable catalyst in aqueous solution
Wang, Min,Zhang, Ting T.,Liang, Yan,Gao, Jing J.
experimental part, p. 835 - 839 (2012/07/28)
Copper benzenesulfonate was found to be an effective catalyst for one-pot three-component cyclocon-densation of isatoic anhydride, aromatic aldehydes, and ammonium salts or primary amines in aqueous solution to afford the corresponding mono- and disubstituted 2,3-dihydroquinazolin-4(1H)-ones in good yields. The catalyst is reusable and could be recycled for several times without distinct decrease in its efficiency. Springer-Verlag 2011.
Cation-exchange resin as an efficient hetero- Geneous catalyst for one-pot three-component synthesis of 2,3-dihydro-4(1H)-quinazolinones
Wang,Zhang,Gao,Liang
, p. 897 - 902 (2013/01/15)
Various mono- and disubstituted 2,3-dihydro-4(1H)-quinazolinones were synthesized efficiently by a one-pot three-component condensation of isatoic anhydride, aromatic aldehydes, and ammonium salts or primary amines using a strong acidic cation-exchange resin as the catalyst in EtOH-H2O solution. The catalyst is cheap, efficient, stable, and reusable under the reaction conditions. The novel method offers several advantages, such as excellent yields, environmentally friendly reaction media, and simple procedure.
Silica supported zinc (II) chloride (SiO2-ZnCl2) as an efficient catalyst for the eco-friendly synthesis of 2,3-dihydroquinazolin- 4(1 H)-ones
Ghashang, Majid
, p. 1213 - 1218 (2013/02/23)
Silica supported zinc (II) chloride (SiO2-ZnCl2) as an efficient and non-toxic heterogeneous catalyst have been used for the simple and facile synthesis of 2,3-dihydroquinazolin-4(1H)-ones through the direct cyclo-condensation of anthranilamide and aldehydes or one-pot three-component cyclo-condensation of isatoic anhydride, ammonium acetate (or amines) and aldehydes under solvent-free conditions.
Efficient synthesis of mono- and disubstituted 2,3-dihydroquinazolin-4(1H)- ones using aluminum methanesulfonate as a reusable catalyst
Song, Zhiguo,Liu, Lianli,Wang, Yang,Sun, Xiaohu
experimental part, p. 1091 - 1099 (2012/09/07)
A wide range of mono- and disubstituted 2,3-dihydroquinazolin-4(1H)-ones were synthesized via a one-pot three components condensation of isatoic anhydride, aldehydes, and ammonium salts or primary amines in the presence of aluminum methanesulfonate in EtOH/H2O solution. The catalyst is reusable and could be recycled for several runs without any distinct decrease in its efficiency. A plausible mechanism for this one-pot three components reaction was proposed. Springer Science+Business Media B.V. 2011.
ZnO nanoparticles catalyzed efficient one-pot three-component synthesis of 2,3-disubstituted quinalolin-4(1H)-ones under solvent-free conditions
Yavari,Beheshti
experimental part, p. 1030 - 1035 (2012/02/04)
ZnO nanoparticles were prepared and applied as a favorable catalyst in three-component one-pot cyclocondensation reaction of isatoic anhydride with amines and aldehydes to afford the corresponding 2,3-disubstituted quinalolin-4(1H)-ones in good yields. Reactions occurred under solvent-free conditions in high atom economy.
Efficient one-pot synthesis of 2,3-dihydroquinazolin-4(1H)-ones from aromatic aldehydes and their one-pot oxidation to quinazolin-4(3H)-ones catalyzed by Bi(NO3)3·5H2O: Investigating the role of the catalyst
Mohammadpoor-Baltork, Iraj,Khosropour, Ahmad R.,Moghadam, Majid,Tangestaninejad, Shahram,Mirkhani, Valiollah,Baghersad, Saeid,Mirjafari, Arsalan
experimental part, p. 944 - 952 (2012/04/23)
An efficient and novel synthesis of 2,3-disubstituted 2,3- dihydroquinazolin-4(1H)-ones via one-pot, three-component reaction of isatoic anhydride, primary amines and aromatic aldehydes catalyzed by Bi(NO 3)3·5H2O under so
One-pot synthesis of 2,3-disubstituted-2,3-dihydroquinazolin-4(1H)-ones using [Hmim][NO3]: An eco-friendly protocol
Mohammadpoor-Baltork, Iraj,Khosropour, Ahmad Reza,Moghadam, Majid,Tangestaninejad, Shahram,Mirkhani, Valiollah,Soltani, Mohammad,Mirjafari, Arsalan
experimental part, p. 1419 - 1427 (2011/12/21)
An efficient method for the synthesis of a series of 2,3-disubstituted-2,3- dihydroquinazolin-4(1H)-ones is described via one-pot condensation reaction of isatoic anhydride, aryl aldehydes, and primary amines using a Bronsted acidic ionic liquid, [Hmim][N
