Recent Advances on Diversity Oriented Heterocycle Synthesis of Fused Quinazolinones

被引:0
作者
Alhalafi, Mona H. [1 ]
机构
[1] Majmaah Univ, Coll Sci Al Zulfi, Dept Chem, PO 66, Al Majmaah 11952, Saudi Arabia
关键词
Quinazolin-2-one; pyrroloquinazolin-2-one; indoloquinazolin-4-one; azepinoquinazolin-4-one; ONE-POT SYNTHESIS; IODINE-CATALYZED SYNTHESIS; VISIBLE-LIGHT; DERIVATIVES; EFFICIENT; CYCLIZATION; ACCESS; GROWTH; COPPER; ARYL;
D O I
10.1080/10406638.2023.2290178
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
During the last decade quinazolinones derivatives have been shown to be useful building blocks for the synthesis of a variety of functionalized polynuclear heterocyclic systems. This review presents the recent systematic and comprehensive literature survey of fused quinazolinones synthesis. These fused heterocycles are classified according to the ring volume starting from three membered up to seven membered cycles and divided according to the number of heteroatoms and type or position of these heteroatoms.
引用
收藏
页码:7109 / 7167
页数:59
相关论文
共 132 条
[21]   Exploring Epidermal Growth Factor Receptor (EGFR) Inhibitor Features: The Role of Fused Dioxygenated Rings on the Quinazoline Scaffold [J].
Chilin, Adriana ;
Conconi, Maria Teresa ;
Marzaro, Giovanni ;
Guiotto, Adriano ;
Urbani, Luca ;
Tonus, Francesca ;
Parnigotto, Pierpaolo .
JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (04) :1862-1866
[22]   Synthesis of quinazolinones and quinazolines [J].
Connolly, DJ ;
Cusack, D ;
O'Sullivan, TP ;
Guiry, PJ .
TETRAHEDRON, 2005, 61 (43) :10153-10202
[23]   Late-Stage C-H Arylation of Thiazolo[5,4-f]quinazolin-9(8H)-one Backbone: Synthesis of an Array of Potential Kinase Inhibitors [J].
Couly, Florence ;
Dubouilh-Benard, Carole ;
Besson, Thierry ;
Fruit, Corinne .
SYNTHESIS-STUTTGART, 2017, 49 (20) :4615-4622
[24]   Synthesis and conformational analysis of new naphth[1,2-e][1,3]oxazino[3,4-c]quinazoline derivatives [J].
Csuetoertoeki, Renata ;
Szatmari, Istvan ;
Koch, Andreas ;
Heydenreich, Matthias ;
Kleinpeter, Erich ;
Fueloep, Ferenc .
TETRAHEDRON, 2011, 67 (44) :8564-8571
[25]   Quinazoline alkaloids in nature [J].
D'yakonov A.L. ;
Telezhenetskaya M.V. .
Chemistry of Natural Compounds, 1997, 33 (3) :221-267
[26]  
Darwish M.K., 2017, LIBYAN J SCI TECHNOL, V6, P8
[27]   Catalyst-free synthesis of quinazolin-4-ones from (hetero)aryl-guanidines: application to the synthesis of pyrazolo[4,3-f]quinazolin-9-ones, a new family of DYRK1A inhibitors [J].
Debray, Julien ;
Bonte, Simon ;
Lozach, Olivier ;
Meijer, Laurent ;
Demeunynck, Martine .
MOLECULAR DIVERSITY, 2012, 16 (04) :659-667
[28]   Montmorillonite K-10 catalyzed cyclization of N-ethoxycarbonyl-N′-arylguanidines: Access to pyrimido[4,5-c]carbazole and pyrimido[5,4-b]indole derivatives [J].
Debray, Julien ;
Zeghida, Walid ;
Baldeyrou, Brigitte ;
Mahieu, Christine ;
Lansiaux, Amelie ;
Demeunynck, Martine .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (14) :4244-4247
[29]  
Demeunynck M, 2013, CURR MED CHEM, V20, P794
[30]  
Du Ha J, 2005, B KOREAN CHEM SOC, V26, P959