The quinazoline-2,4(1H,3H)-diones skeleton: A key intermediate in drug synthesis

被引:9
|
作者
Gheidari, Davood [1 ]
Mehrdad, Morteza [1 ]
Maleki, Saloomeh [2 ]
机构
[1] Univ Guilan, Fac Sci, Dept Chem, Rasht, Iran
[2] Univ Shahrood, Fac Sci, Dept Chem, Shahrud, Iran
来源
关键词
Quinazoline-2; 4(1H; 3H)-dione; Dichloroquinazoline; IN-VITRO; BIOLOGICAL EVALUATION; CELL-PROLIFERATION; DERIVATIVES; DISCOVERY; QUINAZOLINE; INHIBITORS; POTENT; DESIGN; RECEPTOR;
D O I
10.1016/j.scp.2022.100696
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Quinazoline-2,4(1H,3H)-dione is a major class of N-fused heterocyclic with a wide range of biological functions, including anti-HIV, anticancer, antifungal, antibacterial, antimutagenic, anticoccidial, anticonvulsant, anti-inflammatory, antidepressant, antimalarial, antioxidant, antileukemic, and antileishmanial activities, and other activities, has attracted high attention in organic and medicinal chemistry. As a consequence, all chemists and pharmaceutical chemists should be familiar with the various procedures for producing quinazoline-2,4(1H,3H)-dione. The main purpose of this paper is to provide an overview of the many manufacturing methods for various biological compounds based on the quinazoline-2,4(1H,3H)-dione and 2,4-dichloroquinazoline cores.
引用
收藏
页数:45
相关论文
共 50 条
  • [21] Synthesis of some quinazoline-2(1H),4(3H)-dione derivatives
    Abdel-Razik, HH
    JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 2005, 52 (01) : 141 - 148
  • [22] Cesium carbonate catalyzed efficient synthesis of quinazoline-2,4(1H,3H)-diones using carbon dioxide and 2-aminobenzonitriles
    Patil, Yogesh P.
    Tambade, Pawan J.
    Jagtap, Sachin R.
    Bhanage, Bhalchandra M.
    GREEN CHEMISTRY LETTERS AND REVIEWS, 2008, 1 (02) : 127 - 132
  • [23] Fixation of CO2 in structurally diverse quinazoline-2,4(1H,3H)-diones under ambient conditions
    Zhu, Anlian
    Tang, Mingjie
    Lv, Qingzhang
    Li, Lingjun
    Bai, Shukun
    Li, Qianqian
    Feng, Wanlu
    Li, Qixing
    Wang, Jianji
    JOURNAL OF CO2 UTILIZATION, 2019, 34 : 500 - 506
  • [24] Synthesis of diversely substituted quinazoline-2,4(1H,3H)-diones by cyclization of tert-butyl (2-cyanoaryl)carbamates
    Kovela, Satish
    Karad, Somnath
    Tatipudi, V. V. Ganesh
    Arumugam, Karthikeyan
    Somwanshi, Atul Vijay
    Muthukumar, M.
    Mathur, Arvind
    Tester, Richland
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2024, 22 (32) : 6495 - 6499
  • [25] Choline hydroxide promoted chemical fixation of CO2 to quinazoline-2,4(1H,3H)-diones in water
    Lu, Wenjing
    Ma, Jun
    Hu, Jiayin
    Zhang, Zhaofu
    Wu, Congyi
    Han, Buxing
    RSC ADVANCES, 2014, 4 (92) : 50993 - 50997
  • [26] Synthesis of quinazolinophanes containing bridgehead nitrogen atoms from quinazoline-2,4(1H,3H)-dione
    Sharma, R. L.
    Singh, Jasbir
    Kumar, Surinder
    Kour, Daljeet
    Sachar, Anand
    Shallu
    Poonam
    Bhawana
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2007, 44 (06) : 1501 - 1504
  • [27] ELECTRON-IMPACT MASS-SPECTROMETRY OF 1,3-DISUBSTITUTED QUINAZOLINE-2,4(1H,3H)-DIONES
    AKGUN, H
    HOLLSTEIN, U
    ORGANIC MASS SPECTROMETRY, 1990, 25 (05): : 289 - 290
  • [28] ZnO nanoparticles supported on dendritic fibrous nanosilica as efficient catalysts for the one-pot synthesis of quinazoline-2,4(1H,3H)-diones
    Shamsa, Farzaneh
    Motavalizadehkakhky, Alireza
    Zhiani, Rahele
    Mehrzad, Jamshid
    Hosseiny, Malihe Sadat
    RSC ADVANCES, 2021, 11 (59) : 37103 - 37111
  • [29] Highly Efficient Synthesis of Quinazoline-2,4(1H,3H)-diones from CO2 by Hydroxyl Functionalized Aprotic Ionic Liquids
    Shi, Guiling
    Chen, Kaihong
    Wang, Yongtao
    Li, Haoran
    Wang, Congmin
    ACS SUSTAINABLE CHEMISTRY & ENGINEERING, 2018, 6 (05): : 5760 - 5765
  • [30] Efficient synthesis of 2-oxazolidinones and quinazoline-2,4(1H,3H)-diones from CO2 catalyzed by tetrabutylammonium fluoride
    Fujii, Akira
    Matsuo, Hideaki
    Choi, Jun-Chul
    Fujitani, Tadahiro
    Fujita, Ken-ichi
    TETRAHEDRON, 2018, 74 (24) : 2914 - 2920