Synthesis of 3-Nitro-2-arylimidazo[1,2-a]pyridines Using Sodium Dichloroiodide

被引:16
作者
Jagadhane, Prashant B. [1 ]
Telvekar, Vikas N. [1 ]
机构
[1] Inst Chem Technol, Dept Pharmaceut Sci & Technol, Bombay 400019, Maharashtra, India
关键词
2-aminopyridine; nitrostyrene; iodine reagent; 3-nitro-2-arylimidazo[1,2-a]pyridines; DERIVATIVES; DESIGN; EXPLORATION; INHIBITORS; POTENT; AIR;
D O I
10.1055/s-0034-1379185
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Moderate to good yields of various 3-nitro-2-arylimidazo[1,2-a]pyridines have been easily achieved in the reaction of 2-aminopyridines and nitrostyrenes in the presence of sodium dichloriodide. The procedure is simple and various functional groups are tolerated in this reaction system.
引用
收藏
页码:2636 / 2638
页数:3
相关论文
共 23 条
[1]   RESEARCH ON HETEROCYCLIC-COMPOUNDS .32. SYNTHESIS AND CYCLOOXYGENASE-INDEPENDENT ANTIINFLAMMATORY AND ANALGESIC ACTIVITY OF IMIDAZO[1,2-A]PYRIMIDINE DERIVATIVES [J].
ABIGNENTE, E ;
SACCHI, A ;
LANERI, S ;
ROSSI, F ;
DAMICO, M ;
BERRINO, L ;
CALDERARO, V ;
PARRILLO, C .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 1994, 29 (04) :279-286
[2]   Design, synthesis and in vitro antimicrobial evaluation of novel Imidazo[1,2-a]pyridine and imidazo[2,1-b][1,3]benzothiazole motifs [J].
Al-Tel, Taleb H. ;
Al-Qawasmeh, Raed A. ;
Zaarour, Rania .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2011, 46 (05) :1874-1881
[3]   N-Fused Imidazoles As Novel Anticancer Agents That Inhibit Catalytic Activity of Topoisomerase IIα and Induce Apoptosis in G1/S Phase [J].
Baviskar, Ashish T. ;
Madaan, Chetna ;
Preet, Ranjan ;
Mohapatra, Purusottam ;
Jain, Vaibhav ;
Agarwal, Amit ;
Guchhait, Sankar K. ;
Kundu, Chanakya N. ;
Banerjee, Uttam C. ;
Bharatam, Prasad V. .
JOURNAL OF MEDICINAL CHEMISTRY, 2011, 54 (14) :5013-5030
[4]   Exploration of versatile reactions on 2-chloro-3-nitroimidazo[1,2-a]pyridine: expanding structural diversity of C2-and C3-functionalized imidazo[1,2-a]pyridines [J].
Bazin, Marc-Antoine ;
Marhadour, Sophie ;
Tonnerre, Alain ;
Marchand, Pascal .
TETRAHEDRON LETTERS, 2013, 54 (39) :5378-5382
[5]   Imidazo[1,2-a]pyridin-3-amines as potential HIV-1 non-nucleoside reverse transcriptase inhibitors [J].
Bode, Moira L. ;
Gravestock, David ;
Moleele, Simon S. ;
van der Westhuyzen, Christiaan W. ;
Pelly, Stephen C. ;
Steenkamp, Paul A. ;
Hoppe, Heinrich C. ;
Khan, Tasmiyah ;
Nkabinde, Lindiwe A. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2011, 19 (14) :4227-4237
[6]   Design, synthesis and bioevaluation of dihydropyrazolo[3,4-b]pyridine and benzo[4,5]imidazo[1,2-a]pyrimidine compounds as dual KSP and Aurora-A kinase inhibitors for anti-cancer agents [J].
Fu, Rong-geng ;
You, Qi-dong ;
Yang, Lei ;
Wu, Wu-tong ;
Jiang, Cheng ;
Xu, Xiao-li .
BIOORGANIC & MEDICINAL CHEMISTRY, 2010, 18 (22) :8035-8043
[7]   Imidazopyridine-fused [1,3] -diazepinones: Synthesis and antiproliferative activity [J].
Gallud, Audrey ;
Vaillant, Ophelie ;
Maillard, Ludovic T. ;
Arama, Dominique P. ;
Dubois, Joelle ;
Maynadier, Marie ;
Lisowski, Vincent ;
Garcia, Marcel ;
Martinez, Jean ;
Masurier, Nicolas .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2014, 75 :382-390
[8]   Hybrid furoxanyl N-acylhydrazone derivatives as hits for the development of neglected diseases drug candidates [J].
Hernandez, Paola ;
Rojas, Rosario ;
Gilman, Robert H. ;
Sauvain, Michel ;
Lima, Lidia M. ;
Barreiro, Eliezer J. ;
Gonzalez, Mercedes ;
Cerecetto, Hugo .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2013, 59 :64-74
[9]   Three-component direct synthesis of substituted pyrroles from easily accessible chemical moieties using hypervalent iodine reagent [J].
Jadhav, Nikhil C. ;
Jagadhane, Prashant B. ;
Patile, Hemlata V. ;
Telvekar, Vikas N. .
TETRAHEDRON LETTERS, 2013, 54 (23) :3019-3021
[10]   Synthesis of GABAA receptor agonists and evaluation of their α-subunit selectivity and orientation in the GABA binding site [J].
Jansen, Michaela ;
Rabe, Holger ;
Strehle, Axelle ;
Dieler, Sandra ;
Debus, Fabian ;
Dannhardt, Gerd ;
Akabas, Myles H. ;
Lueddens, Hartmut .
JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (15) :4430-4448