HPW-Catalyzed environmentally benign approach to imidazo[1,2-a]pyridines

被引:1
|
作者
Martinho, Luan A. [1 ]
Andrade, Carlos Kleber Z. [1 ]
机构
[1] Univ Brasilia, Lab Quim Metodol & Organ Sintet LaQMOS, Inst Quim, BR-70904970 Brasilia, DF, Brazil
来源
关键词
GBB-3CR; imidazo[1,2-a]pyridine; microwave; phosphotungstic acid; BIENAYME MULTICOMPONENT REACTION; ONE-POT SYNTHESIS; DERIVATIVES; DISCOVERY; SOLVENT; PYRAZINES;
D O I
10.3762/bjoc.20.55
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The imidazo[1,2-a]pyridine moiety is present in drugs with several biological activities. The most direct way of obtaining this nucleus is the Groebke-Blackburn-Bienayme three -component reaction (GBB-3CR) between aminopyridines, aldehydes, and isocyanides under both Lewis and Bronsted acid catalysis. However, several catalysts for this reaction have major drawbacks such as being expensive, extremely dangerous, strong oxidizing, and even explosive. In this scenario, heteropolyacids emerge as greener and safer alternatives due to their very strong Bronsted acidity. In particular, phosphotungstic acid (HPW) is an economical and green attractive catalyst for being cheap, non-toxic, and is known for its chemical and thermal stability. Herein, we report a straightforward approach to the GBB-3CR using HPW as catalyst in ethanol under microwave (mu w) heating. This convenient environmentally benign methodology is broad in scope, provides the heterobicyclic products in high yields (up to 99%), with a low catalyst loading (2 mol %) in only 30 minutes, and allows the successful use of aliphatic aldehydes, substrates not so frequently explored with most usual catalysts for this reaction. Furthermore, the aforementioned advantages make this methodology very attractive and superior to the existing ones.
引用
收藏
页码:628 / 637
页数:10
相关论文
共 50 条
  • [41] Copper-catalyzed C-N bond formation with imidazo[1,2-a]pyridines
    Sun, Kai
    Mu, Shiqiang
    Liu, Zhenhua
    Feng, Ranran
    Li, Yali
    Pang, Kui
    Zhang, Bing
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2018, 16 (36) : 6655 - 6658
  • [42] Cu-Catalyzed Synthesis of 3-Formyl Imidazo[1,2-a]pyridines and Imidazo[1,2-a]pyrimidines by Employing Ethyl Tertiary Amines as Carbon Sources
    Rao, Changqing
    Mai, Shaoyu
    Song, Qiuling
    ORGANIC LETTERS, 2017, 19 (18) : 4726 - 4729
  • [43] Imidazo[1,2-a]pyridines with potent activity against herpesviruses
    Gudmundsson, Kristian S.
    Johns, Brian A.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2007, 17 (10) : 2735 - 2739
  • [44] Approaches to the Syntheses of Partially Reduced Imidazo[1,2-a]pyridines
    Shin, Junhwa
    Nho, Young Chang
    Howard, Arthur S.
    BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2008, 29 (10) : 1998 - 2004
  • [45] Nitrosylation of imidazo[1,2-a] pyridines in metal free system
    Hao, Xin-Qi
    Liu, Wen-Bo
    Shen, Xiao-Jing
    Wang, Wei
    Liang, Zhi-Kun
    Zhu, Xinju
    Song, Mao-Ping
    JOURNAL OF SAUDI CHEMICAL SOCIETY, 2017, 21 (01) : 91 - 94
  • [46] Electrochemical oxidative selenylation of imidazo[1,2-a]pyridines with diselenides
    Kim, Yeon Joo
    Kim, Dae Young
    TETRAHEDRON LETTERS, 2019, 60 (10) : 739 - 742
  • [47] Solution and solid phase functionalization of imidazo[1,2-a]pyridines
    El Kazzouli, S
    Berthault, A
    Berteina-Raboin, S
    Mouaddib, A
    Guillaumet, G
    LETTERS IN ORGANIC CHEMISTRY, 2005, 2 (02) : 184 - 187
  • [48] Functionalization of imidazo[1,2-a]pyridines via radical reactions
    Ma, Chun-Hua
    Chen, Ming
    Feng, Zhi-Wen
    Zhang, Yan
    Wang, Jin
    Jiang, Yu-Qin
    Yu, Bing
    NEW JOURNAL OF CHEMISTRY, 2021, 45 (21) : 9302 - 9314
  • [49] C3-Functionalization of Imidazo[1,2-a]pyridines
    Tashrifi, Zahra
    Mohammadi-Khanaposhtani, Mohammad
    Larijani, Bagher
    Mahdavi, Mohammad
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2020, 2020 (03) : 269 - 284
  • [50] Copper-Catalyzed Multicomponent Reactions (MCRs) for Disulfenylation of Imidazo[1,2-a]pyridines Using Elemental Sulfur and Arylhalides and Intramolecular Cyclization of Haloinnidazo[1,2-a]pyridines
    Semwal, Rashmi
    Ravi, Chitrakar
    Saxena, Soumya
    Adimurthy, Subbarayappa
    JOURNAL OF ORGANIC CHEMISTRY, 2019, 84 (21): : 14151 - 14160