Silica sulfuric acid as an efficient and recoverable catalyst for the synthesis of trisubstituted imidazoles

被引:167
作者
Shaabani, A [1 ]
Rahmati, A [1 ]
机构
[1] Shahid Beheshti Univ, Dept Chem, Tehran, Iran
关键词
imidazole; silica sulfuric acid; one-pot condensation reaction; solid acid catalyst; water;
D O I
10.1016/j.molcata.2006.01.006
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Trisubstituted imidazoles have been synthesized in high yields in the presence of silica sulfuric acid as a catalyst. The reaction is carried out in water, a very green solvent, under reflux conditions. The reaction work-up is simple and the catalyst is easily separated from the products by filtration. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:246 / 248
页数:3
相关论文
共 30 条
[1]   An efficient synthesis of tetrasubstituted imidazoles from N-(2-oxo)-amides [J].
Claiborne, CF ;
Liverton, NJ ;
Nguyen, KT .
TETRAHEDRON LETTERS, 1998, 39 (49) :8939-8942
[2]  
CONSONNI R, 1991, J CHEM RES-S, P188
[3]   SULFONYLUREAS AND SULFONYLCARBAMATES AS NEW NON-TETRAZOLE ANGIOTENSIN-II RECEPTOR ANTAGONISTS - DISCOVERY OF A HIGHLY POTENT ORALLY-ACTIVE (IMIDAZOLYLBIPHENYLYL) SULFONYLUREA (HR-720) [J].
DEPREZ, P ;
GUILLAUME, J ;
BECKER, R ;
CORBIER, A ;
DIDIERLAURENT, S ;
FORTIN, M ;
FRECHET, D ;
HAMON, G ;
HECKMANN, B ;
HEITSCH, H ;
KLEEMANN, HW ;
VEVERT, JP ;
VINCENT, JC ;
WAGNER, A ;
ZHANG, JD .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (13) :2357-2377
[4]   SYNTHESIS OF DIPHTHAMIDE - THE TARGET OF DIPHTHERIA-TOXIN CATALYZED ADP-RIBOSYLATION IN PROTEIN-SYNTHESIS ELONGATION FACTOR-II [J].
EVANS, DA ;
LUNDY, KM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (04) :1495-1496
[5]   Synthesis of substituted imidazoles via organocatalysis [J].
Frantz, DE ;
Morency, L ;
Soheili, A ;
Murry, JA ;
Grabowski, EJJ ;
Tillyer, RD .
ORGANIC LETTERS, 2004, 6 (05) :843-846
[6]  
Grimmett M.R., 1996, Comprehensive Heterocyclic Chemistry, P77
[7]  
GRIMMETT MR, 1984, COMPREHENSIVE HETERO, V5, P475
[8]  
Japp F.R., 1882, BER DTSCH CHEM GES, V15, P1268
[9]   A facile synthesis of fluorine-containing heterocycles - Use of 1,1,1-trifluoro-2-alkanones as a convenient synthetic intermediate [J].
Kamitori, Y .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 2001, 38 (03) :773-776
[10]   A modified procedure for the synthesis of 1-arylimidazoles [J].
Liu, JP ;
Chen, JB ;
Zhao, JF ;
Zhao, YH ;
Li, L ;
Zhang, HB .
SYNTHESIS-STUTTGART, 2003, (17) :2661-2666