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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 36, 2006 - Issue 15
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Original Articles

Convergent One‐Pot Synthesis of 3‐Substituted Quinazolin‐4(3H)‐ones under Solvent‐Free Conditions

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Pages 2245-2252 | Received 07 Oct 2005, Published online: 16 Feb 2007

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Samir Y. Abbas, Khairy A. M. El-Bayouki & Wahid M. Basyouni. (2016) Utilization of isatoic anhydride in the syntheses of various types of quinazoline and quinazolinone derivatives. Synthetic Communications 46:12, pages 993-1035.
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Articles from other publishers (13)

Vakhid A. Mamedov, Vera L. Mamedova, Victor V. Syakaev, Aidar T. Gubaidullin, Julia K. Voronina, Temur A. Kushatov, Dmitry E. Korshin, Aida I. Samigullina, Ekaterina G. Tanysheva, Il'dar Kh. Rizvanov & Shamil K. Latypov. (2021) New and efficient synthesis of 3-arylquinazolin-4(1H)-ones and biologically important N-fused tetracycles based on N-(2-carboxyphenyl)oxalamide. Tetrahedron Letters 82, pages 153327.
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Xiangyu Zhang, Chujun Luo, Xiaoyong Chen, Weilin Ma, Bin Li, Zirui Lin, Xiuwen Chen, Yibiao Li & Feng Xie. (2021) Direct synthesis of quinazolinones via the carbon-supported acid-catalyzed cascade reaction of isatoic anhydrides with amides and aldehydes. Tetrahedron Letters 66, pages 152835.
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Malavattu G. Prasad, C. Vijaya Lakshmi, Naresh K. Katari, Sreekantha B. Jonnalagadda & Manojit Pal. (2020) Lemon Juice Mediated Synthesis of 3-Substituted Quinazolin-4(3H)-Ones and their Pharmacological Evaluation. Anti-Cancer Agents in Medicinal Chemistry 19:16, pages 2001-2009.
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Zahra Tashrifi, Mohammad Mohammadi-Khanaposhtani, Mahmood Biglar, Bagher Larijani & Mohammad Mahdavi. (2019) Isatoic Anhydride: A Fascinating and Basic Molecule for the Synthesis of Substituted Quinazolinones and Benzo di/triazepines. Current Organic Chemistry 23:10, pages 1090-1130.
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Tej Narayan Poudel, Hari Datta Khanal & Yong Rok Lee. (2018) Base-promoted ring opening of 3-chlorooxindoles for the construction of 2-aminoarylthioates and their transformation to quinazolin-4(3 H )-ones . New Journal of Chemistry 42:6, pages 4735-4741.
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Mohsen Dadgar & Nasim Milani Kalkhorani. (2015) Efficient and Practical One-Pot Route to Synthesise Quinazolin4(3H)-Ones Using Trifluoromethanesulfonic Anhydride and 2-Chloropyridine. Journal of Chemical Research 39:2, pages 120-122.
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K. Raghavendra Rao, Akula Raghunadh, Ramamohan Mekala, Suresh Babu Meruva, T.V. Pratap, T. Krishna, Dipak Kalita, Eppakayala Laxminarayana, Bagineni Prasad & Manojit Pal. (2014) Glyoxylic acid in the reaction of isatoic anhydride with amines: a rapid synthesis of 3-(un)substituted quinazolin-4(3H)-ones leading to rutaecarpine and evodiamine. Tetrahedron Letters 55:43, pages 6004-6006.
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Chandresh L. Jagani, Natvar A. Sojitra, Satish F. Vanparia, Tarosh S. Patel, Ritu B. Dixit & Bharat C. Dixit. (2012) Microwave promoted synthesis and antimicrobial activity of 3-thiazole substituted 2-styryl-4(3H)-quinazolinone derivatives. Journal of Saudi Chemical Society 16:4, pages 363-369.
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Hitesh B. Jalani, Amit N. Pandya, Dhaivat H. Pandya, Jayesh A. Sharma, V. Sudarsanam & Kamala K. Vasu. (2012) An efficient, greener, and solvent-free one-pot multicomponent synthesis of 3-substituted quinazolin-4(3H)ones and thienopyrimidin-4(3H)ones. Tetrahedron Letters 53:32, pages 4062-4064.
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Maya Shankar Singh & Sushobhan Chowdhury. (2012) Recent developments in solvent-free multicomponent reactions: a perfect synergy for eco-compatible organic synthesis. RSC Advances 2:11, pages 4547.
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Nader Saemian, Omid Khalili Arjomandi & Gholamhossein Shirvani. (2009) Synthesis of a series of carbon-14 labelled 4-aminoquinazolines and quinazolin-4 (3H)-ones. Journal of Labelled Compounds and Radiopharmaceuticals 52:11, pages 453-456.
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Nuno R. Candeias, Luís C. Branco, Pedro M. P. Gois, Carlos A. M. Afonso & Alexandre F. Trindade. (2009) More Sustainable Approaches for the Synthesis of N-Based Heterocycles. Chemical Reviews 109:6, pages 2703-2802.
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Kurosh Rad‐Moghadam, Manoochehr Mamghani & Laleh Samavi. (2006) Convergent One‐Pot Synthesis of 3‐Substituted Quinazolin‐4(3H)‐ones under Solvent‐Free Conditions.. ChemInform 37:46.
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