Mono Arylation of Imidazo[ 1,2-a]pyridine and 1,2-dimethyl Imidazole: Application of Carbon Nitride Supported Palladium Catalyst

被引:17
|
作者
Nandi, Debkumar [1 ]
Siwal, Samarjeet S. [1 ]
Mallick, Kaushik [1 ]
机构
[1] Univ Johannesburg, Dept Chem, POB 524, ZA-2006 Auckland Pk, South Africa
来源
CHEMISTRYSELECT | 2017年 / 2卷 / 05期
基金
新加坡国家研究基金会;
关键词
arylation; carbon nitride; C-H functionalization; imidazo pyridine; imdazole; PHOSPHINE-FREE CONDITIONS; LIGAND-FREE PALLADIUM; IN-SITU SYNTHESIS; ARYL CHLORIDES; EFFICIENT CATALYST; COUPLING REACTION; PD NANOPARTICLES; HECK REACTIONS; HETEROCYCLES; NANOCRYSTALS;
D O I
10.1002/slct.201601837
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbon nitride (gCN) supported nanosized metallic palladium has been prepared, characterized (by various spectroscopic and microscopic techniques) and applied as a catalyst for the mono-arylation of imidazole moieties with broader range of substrates scope. Scaling up of the reaction and recyclability of the catalyst (for 6 cycles) also has been performed for this study. Nitroarene derivatives, produced from the above coupling reaction, could be converted to the corresponding amine derivatives using the same catalyst under mild reaction condition.
引用
收藏
页码:1747 / 1752
页数:6
相关论文
共 50 条
  • [21] Synthesis and properties of cyanomethyl derivatives of imidazo[1,2-a]pyridine, imidazo[1,2-a]pyrimidine, and imidazo[2,1-b]thiazole
    Kutrov, G. P.
    Kovalenko, N. V.
    Volovenko, Yu. M.
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2008, 44 (02) : 257 - 262
  • [22] Synthesis and properties of cyanomethyl derivatives of imidazo[1,2-a]pyridine, imidazo[1,2-a]pyrimidine, and imidazo[2,1-b]thiazole
    G. P. Kutrov
    N. V. Kovalenko
    Yu. M. Volovenko
    Russian Journal of Organic Chemistry, 2008, 44 : 257 - 262
  • [23] SRN1 REACTIONS IN IMIDAZO[1,2-A]PYRIDINE SERIES
    VANELLE, P
    MALDONADO, J
    MADADI, N
    GUEIFFIER, A
    TEULADE, JC
    CHAPAT, JP
    CROZET, MP
    TETRAHEDRON LETTERS, 1990, 31 (21) : 3013 - 3016
  • [24] IMIDAZO[1,2-B]PYRIDAZINES .18. SYNTHESES AND CENTRAL-NERVOUS-SYSTEM ACTIVITIES OF SOME 6-(CHLORO AND METHOXY)IMIDAZO[1,2-A]PYRIDINE, 7-(CHLORO AND METHOXY)IMIDAZO[1,2-A]PYRIDINE AND 8-(CHLORO AND METHOXY)IMIDAZO[1,2-A]PYRIDINE ANALOGS
    BARLIN, GB
    DAVIES, LP
    HARRISON, PW
    AUSTRALIAN JOURNAL OF CHEMISTRY, 1995, 48 (05) : 1031 - 1038
  • [25] Synthesis of imidazo[1,2-a] pyridine derivatives as antiviral agents
    Mavel, S
    Renou, JL
    Galtier, C
    Snoeck, R
    Andrei, G
    Balzarini, J
    De Clercq, E
    Gueiffier, A
    ARZNEIMITTEL-FORSCHUNG-DRUG RESEARCH, 2001, 51 (04): : 304 - 309
  • [26] Medicinal Attributes of Imidazo[1,2-a] pyridine Derivatives: An Update
    Devi, Nisha
    Singh, Dharmender
    Rawal, Ravindra K.
    Bariwal, Jitender
    Singh, Virender
    CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2016, 16 (26) : 2963 - 2994
  • [27] PREPARATION OF SOME SUBSTITUTED IMIDAZO[1,2-A]PYRIDINE DERIVATIVES
    SHAWCROSS, AP
    STANFORTH, SP
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 1993, 30 (02) : 563 - 565
  • [28] Design and synthesis of new imidazo[1,2-a]pyridine and imidazo [1,2-a]pyrazine derivatives with antiproliferative activity against melanoma cells
    Garamvoelgyi, Rita
    Dobos, Judit
    Sipos, Anna
    Boros, Sandor
    Illyes, Eszter
    Baska, Ferenc
    Kekesi, Laszlo
    Szabadkai, Istvan
    Szantai-Kis, Csaba
    Keri, Gyorgy
    Orfi, Laszlo
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2016, 108 : 623 - 643
  • [29] TELE-AMINATION OF IMIDAZO[1,2-A]PYRIDINE SYSTEM
    HAND, ES
    PAUDLER, WW
    JOURNAL OF ORGANIC CHEMISTRY, 1978, 43 (14): : 2900 - 2906
  • [30] Imidazo[1,2-a]pyridine Scaffold as Prospective Therapeutic Agents
    Deep, Aakash
    Bhatia, Richa Kaur
    Kaur, Ramanjot
    Kumar, Sanjiv
    Jain, Upendra Kumar
    Singh, Harinder
    Batra, Sandeep
    Kaushik, Dinesh
    Deb, Pran Kishore
    CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2017, 17 (02) : 238 - 250