A revisit to the Hantzsch reaction: Unexpected products beyond 1,4-dihydropyridines

被引:85
作者
Shen, Li [1 ]
Cao, Song [1 ]
Wu, Jingjing [1 ]
Zhang, Jian [1 ]
Li, Hui [1 ]
Liu, Nianjin [1 ]
Qian, Xuhong [1 ]
机构
[1] E China Univ Sci & Technol, Shanghai Key Lab Chem Biol, Ctr Fluorine Chem Technol, Sch Pharm, Shanghai 200237, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
ONE-POT SYNTHESIS; SOLVENT-FREE; POLYHYDROQUINOLINE DERIVATIVES; 3-COMPONENT SYNTHESIS; HIGHLY EFFICIENT; AROMATIZATION; CONVENIENT; PYRAZOLES; BIGINELLI; PYRIDINES;
D O I
10.1039/b906358g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel green and efficient one-pot three-component synthesis of 2-aryl-pyridines in good to excellent yields has been reported. The methodology initially involved the formation of 1,2-dihydropyridine intermediates via reaction of a variety of aromatic aldehydes with ethyl (methyl) acetoacetate and ammonium acetate, which were the same starting materials as the Hantzsch reaction, under solvent-, catalyst-and heat-free (at room temperature) conditions, followed by air oxidation for 72 hours. In this paper, we also systematically reinvestigated the classic Hantzsch reaction under different reaction conditions, analyzed the main products as well as byproducts, corrected some mistakes in the literature and elucidated the reaction mechanism.
引用
收藏
页码:1414 / 1420
页数:7
相关论文
共 51 条
  • [1] Synthesis of 2-substituted pyridines via a regiospecific alkylation, alkynylation, and arylation of pyridine N-oxides
    Andersson, Hans
    Almqvist, Fredrik
    Olsson, Roger
    [J]. ORGANIC LETTERS, 2007, 9 (07) : 1335 - 1337
  • [2] Rearrangement of o-nitrobenzaldehyde in the Hantzsch reaction
    Angeles, E
    Santillán, H
    Menconi, I
    Martínez, I
    Ramírez, A
    Velázquez, A
    López-Castañares, R
    Martínez, R
    [J]. MOLECULES, 2001, 6 (08) : 683 - 693
  • [3] Synthesis of Hantzsch 1,4-dihydropyridines under microwave irradiation
    Anniyappan, M
    Muralidharan, D
    Perumal, PT
    [J]. SYNTHETIC COMMUNICATIONS, 2002, 32 (04) : 659 - 663
  • [4] STUDIES ON DIHYDROPYRIDINES .1. THE PREPARATION OF UNSYMMETRICAL 4-ARYL-1,4-DIHYDROPYRIDINES BY THE HANTZSCH-BEYER SYNTHESIS
    BERSON, JA
    BROWN, E
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (02) : 444 - 447
  • [5] 4-ARYLDIHYDROPYRIDINES, A NEW CLASS OF HIGHLY-ACTIVE CALCIUM-ANTAGONISTS
    BOSSERT, F
    MEYER, H
    WEHINGER, E
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1981, 20 (09): : 762 - 769
  • [6] Magnesium nitride as a convenient source of ammonia: Preparation of dihydropyridines
    Bridgwood, Katy L.
    Veitch, Gemma E.
    Ley, Steven V.
    [J]. ORGANIC LETTERS, 2008, 10 (16) : 3627 - 3629
  • [7] Synthesis of thiohydantoins under one-pot three-component solvent-free conditions
    Cao, Song
    Zhu, Longjie
    Zhao, Chuanmeng
    Tang, Xiuhong
    Sun, Huajun
    Feng, Xin
    Qian, Xuhong
    [J]. MONATSHEFTE FUR CHEMIE, 2008, 139 (08): : 923 - 926
  • [8] Solvent-free, two-step synthesis of some unsymmetrical 4-aryl-1,4-dihydropyridines
    Correa, WH
    Scott, JL
    [J]. GREEN CHEMISTRY, 2001, 3 (06) : 296 - 301
  • [9] Characterizing the 1,4-dihydropyridines binding interactions in the L-type Ca2+ channel:: Model construction and docking calculations
    Cosconati, Sandro
    Marinelli, Luciana
    Lavecchia, Antonio
    Novellino, Ettore
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2007, 50 (07) : 1504 - 1513
  • [10] A simple, green and one-pot four-component synthesis of 1,4-dihydropyridines and their aromatization
    Das Sharma, Saikat
    Hazarika, Parasa
    Konwar, Dilip
    [J]. CATALYSIS COMMUNICATIONS, 2008, 9 (05) : 709 - 714