Wells-Dawson type heteropolyacid catalyzed synthesis of quinoxaline derivatives at room temperature

被引:81
作者
Heravi, Majid M. [1 ]
Bakhtiari, Khadijeh
Bamoharram, Fatemeh F.
Tehrani, Maryam H.
机构
[1] Alzahra Univ, Dept Chem, Sch Sci, Tehran, Iran
[2] Azad Univ Mashhad, Dept Chem, Mashhad, Iran
来源
MONATSHEFTE FUR CHEMIE | 2007年 / 138卷 / 05期
关键词
quinoxalines; 1,2-diketones; o-phenylenediamines; heteropolyacid H6P2W18O62 center dot 24H(2)O; Wells-Dawson;
D O I
10.1007/s00706-007-0594-5
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Wells-Dawson heteropolyacid (H6P2W18O62 center dot 24H(2)O) was used as an effective catalyst for the synthesis of biologically active quinoxaline derivatives from the condensation of o-phenylenediamines with 1,2-dicarbonyl compounds at room temperature in excellent yields.
引用
收藏
页码:465 / 467
页数:3
相关论文
共 30 条
[1]  
Bailly C, 1999, ANTI-CANCER DRUG DES, V14, P291
[2]   Preyssler catalyst,[NaP5W30O110]14- :: A green, efficient and reusable catalyst for esterification of salicylic acid with aliphatic and benzylic alcohols [J].
Bamoharram, FF ;
Heravi, MM ;
Roshani, M ;
Jahangir, M ;
Gharib, A .
APPLIED CATALYSIS A-GENERAL, 2006, 302 (01) :42-47
[3]   Heteropolyacid-based catalysis. Dawson acid for MTBE synthesis in gas phase [J].
Baronetti, G ;
Briand, L ;
Sedran, U ;
Thomas, H .
APPLIED CATALYSIS A-GENERAL, 1998, 172 (02) :265-272
[4]   An efficient protocol for the synthesis of quinoxaline derivatives at room temperature using molecular iodine as the catalyst [J].
Bhosale, RS ;
Sarda, SR ;
Ardhapure, SS ;
Jadhav, WN ;
Bhusare, SR ;
Pawar, RP .
TETRAHEDRON LETTERS, 2005, 46 (42) :7183-7186
[5]  
Brock E. D., 1999, U.S. Patent, Patent No. [WO 9,951,688, WO9951688]
[6]  
Brown D. J., 2004, CHEM HETEROCYCLIC CO
[7]  
Cheeseman G. W. H., 1978, ADV HETEROCYCL CHEM, P367
[8]  
Dailey S, 2001, J MATER CHEM, V11, P2238, DOI 10.1039/b104674h
[9]   STRUCTURE REVISION OF ANTIBIOTIC ECHINOMYCIN [J].
DELL, A ;
WILLIAMS, DH ;
MORRIS, HR ;
SMITH, GA ;
FEENEY, J ;
ROBERTS, GCK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1975, 97 (09) :2497-2502
[10]   Tyrphostins .5. Potent inhibitors of platelet-derived growth factor receptor tyrosine kinase: Structure-activity relationships in quinoxalines, quinolines, and indole tyrphostins [J].
Gazit, A ;
App, H ;
McMahon, G ;
Chen, J ;
Levitzki, A ;
Bohmer, FD .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (11) :2170-2177