知识介绍
|
喹唑啉酮的合成方法
曾庆乐, 魏海东, 周立宏
成都理工大学材料与化学化工学院绿色催化合成研究所 成都 610059
Synthetic Methods of Quinazolinones
ZENG Qing-Le, WEI Hai-Dong, ZHOU Li-Hong
Institute of Green Catalysis and Synthesis, College of Material and Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu 610059, China
摘要: 介绍了以邻氨基苯甲腈、邻氨基芳甲酸、靛红酸酐、邻氨基苯甲酰胺、邻硝基苯甲酰胺、邻碘芳甲酰胺、邻卤苯甲酸、邻卤苯甲腈为底物时喹唑啉酮的合成方法及其研究进展,并对其进行了简要的评述。
关键词: 喹唑啉酮 ,
含氮杂环 ,
合成方法
通讯作者:
曾庆乐
E-mail: qinglezeng@hotmail.com
引用本文:
曾庆乐, 魏海东, 周立宏. 喹唑啉酮的合成方法[J]. 化学教育(中英文), 2016, 37(8): 1-7
[1]
Joule J A, Mills K. Heterocyclic Chemistry at a Glance. 2nd ed. Chichester: John Wiley & Sons, 2013: 167-179
[2]
Mhaske S B, Argade N P. Tetrahedron, 2006, 62(42): 9787-9826
[3]
Henderson F G, Rose C L, Harris P N, et al. J. Pharmacol. Exp. Ther., 1949, 95: 191-200
[4]
张越, 杜会茹,王永国,等. 河北师范大学学报:自然科学版, 2008, 32(4): 510-516
[5]
Connolly D J, Cusack D, O'Sullivan T P, et al. Tetrahedron, 2005, 61(43): 10153-10202
[6]
Witt A, Bergman J. Curr. Org. Chem., 2003, 7(7): 659-677
[7]
周丽霞. 生物灾害科学, 2012, 35(2): 142-148
[8]
Van Zyl E F. Forensic Sci. Int., 2001, 122(2/3): 142-149
[9]
Piller L B, Davis B R, Cutler J A, et al. Curr. Control Trials Cardiovasc. Med., 2002, 3(1): 10
[10]
Mori A, Mukawa J, Okusu H, et al. Brain and Nerve, 1969, 21(3): 271-275
[11]
Jiang J B, Hesson D P, Dusak B A, et al. J. Med. Chem.,1990, 33(6): 1721-1728
[12]
Hennequin L F, Boyle F T, Wardleworth J M. J. Med. Chem., 1996, 39(3): 695-704
[13]
Adib M, Ehsan Sheikhi, Bijanzadeh H R. Synlett., 2012, 23(1): 85-88
[14]
Mohammadi A A, Hossini S S. Chin. J. Chem., 2011, 29(9): 1982-1984
[15]
Abdel-Jalil R J, Voelter W, Saeed M. Tetrahedron Lett., 2004, 45(17): 3475-3476
[16]
Wang G, Miao C, Kang H. Bull. Chem. Soc. Japan, 2006, 79(9): 1426-1430
[17]
Zhan D, Li T, Zhang X, et al. Synth. Commun., 2013, 43(18): 2493-2500
[18]
Zhan D, Li T, Wei H, et al. RSC Adv., 2013, 3(24): 9325-9329
[19]
Cheng R, Guo T, Negrerie D Z, et al. Synthesis, 2013, 45(21): 2998-3006
[20]
Wei H, Li T, Zhou Y, et al. Synthesis, 2013, 45(24): 3349-3354
[21]
Zhao D, Wang T, Li J C. Chem. Comm., 2014, 50(49): 6471-6474
[22]
Zhou J, Fang J. J. Org. Chem., 2011, 76(19): 7730 -7736
[23]
Hikawa H, Yukari Ino, Suzuki H, et al. J. Org. Chem., 2012, 77(16): 7046-7051
[24]
Siddiki S M A H, Kon K, Touchy A S, et al. Catal. Sci. Technol., 2014, 4(6): 1716-1719
[25]
Qiu D, Wang Y, Lu D, et al. Monatsh. Chem., 2015, online first (DOI: 10.1007/s00706-015-1434-7)
[26]
Romero A H, Salazar J, Lopez S E. Synthesis, 2013, 45(14): 2043-2050
[27]
Xu W, Jin Y, Liu H, et al. Org. Lett., 2011, 13(6): 1274-1277
[28]
Xu W, Fu H. J. Org. Chem., 2011, 76(10): 3846-3852
[29]
Wang L X, Xiang J F, Tang Y L. Eur. J. Org. Chem., 2014, 2014(13): 2682-2685
[30]
He W, Zhao H, Yao R, et al. RSC Adv., 2014, 4(91): 50285-50294
[31]
Chai H, Li J, Yang L, et al. RSC Adv., 2014, 4(48): 44811-44814