A Novel Green Synthesis of Thalidomide and Analogs

被引:11
|
作者
Benjamin, Ellis [1 ]
Hijji, Yousef M. [2 ]
机构
[1] Stockton Univ, Dept Chem, 101 Vera King Farris Dr, Galloway, NJ 08205 USA
[2] Qatar Univ, Dept Chem & Earth Sci, POB 2713, Doha, Qatar
关键词
MULTIPLE-MYELOMA; TNF-ALPHA; LENALIDOMIDE MAINTENANCE; EXPRESSION; POMALIDOMIDE; ANTICANCER; IL-1-BETA; IL-10; CELLS; DRUG;
D O I
10.1155/2017/6436185
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Thalidomide and its derivatives are currently under investigation for their antiangiogenic, immunomodulative, and anticancer properties. Current methods used to synthesize these compounds involve multiple steps and extensive workup procedures. Described herein is an efficient microwave irradiation green synthesis method that allows preparation of thalidomide and its analogs in a one-pot multicomponent synthesis system. The multicomponent synthesis system developed involves an array of cyclic anhydrides, glutamic acid, and ammonium chloride in the presence of catalytic amounts of 4-N, N-dimethylaminopyridine (DMAP) to produce thalidomide and structurally related compounds within minutes in good isolated yields.
引用
收藏
页数:6
相关论文
共 50 条
  • [21] Design, synthesis, and biological evaluation of new challenging thalidomide analogs as potential anticancer immunomodulatory agents
    El-Zahabi, Mohamed Ayman
    Sakr, Helmy
    El-Adl, Khaled.
    Zayed, Mohamed
    Abdelraheem, Adel S.
    Eissa, Sally I.
    Elkady, Hazem
    Eissa, Ibrahim H.
    BIOORGANIC CHEMISTRY, 2020, 104
  • [22] 5′-substituted thalidomide analogs as modulators of TNF-α
    Teubert, U
    Zwingenberger, K
    Wnendt, S
    Eger, K
    ARCHIV DER PHARMAZIE, 1998, 331 (01) : 7 - 12
  • [23] Anticancer effects of novel thalidomide analogs in A549 cells through inhibition of vascular endothelial growth factor and matrix metalloproteinase-2
    El-Aarag, Bishoy
    Kasai, Tomonari
    Masuda, Junko
    Agwa, Hussein
    Zahran, Magdy
    Seno, Masaharu
    BIOMEDICINE & PHARMACOTHERAPY, 2017, 85 : 549 - 555
  • [24] Facile Synthesis of Thalidomide
    Binh Duong Vu
    Ngoc Minh Ho Ba
    Dinh Chau Phan
    ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2019, 23 (07) : 1374 - 1377
  • [25] Isosteric analogs of lenalidomide and pomalidomide: Synthesis and biological activity
    Ruchelman, Alexander L.
    Man, Hon-Wah
    Zhang, Weihong
    Chen, Roger
    Capone, Lori
    Kang, Jian
    Parton, Anastasia
    Corral, Laura
    Schafer, Peter H.
    Babusis, Darius
    Moghaddam, Mehran F.
    Tang, Yang
    Shirley, Michael A.
    Muller, George W.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2013, 23 (01) : 360 - 365
  • [26] Synthesis of novel 5,6-dehydrokawain analogs as osteogenic inducers and their action mechanisms
    Kumagai, Momochika
    Nishikawa, Keisuke
    Mishima, Takashi
    Yoshida, Izumi
    Ide, Masahiro
    Koizumi, Keiko
    Nakamura, Munetomo
    Morimoto, Yoshiki
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2017, 27 (11) : 2401 - 2406
  • [27] Differentiation of antiinflammatory and antitumorigenic properties of stabilized enantiomers of thalidomide analogs
    Jacques, Vincent
    Czarnik, Anthony W.
    Judge, Thomas M.
    Van der Ploeg, Lex H. T.
    DeWitt, Sheila H.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (12) : E1471 - E1479
  • [28] Strengthening Molecular Glues: Design Strategies for Improving Thalidomide Analogs as Cereblon Effectors and Anticancer Agents
    Nutt, Michael J.
    Stewart, Scott G.
    DRUG DISCOVERY TODAY, 2024, 29 (06)
  • [29] Thalidomide and its analogs for hemoglobinopathies: two birds with one stone?
    Kutlar, Abdullah
    Meiler, Steffen
    Swerdlow, Paul
    Knight, Robert
    EXPERT REVIEW OF HEMATOLOGY, 2012, 5 (01) : 9 - 11
  • [30] Synthesis, characterization and anti-tumor activity of novel thymoquinone analogs against pancreatic cancer
    Yusufi, Mujahid
    Banerjee, Sanjeev
    Mohammad, Momin
    Khatal, Sandhya
    Swamy, K. Venkateswara
    Khan, Ejazuddin M.
    Aboukameel, Amro
    Sarkar, Fazlul H.
    Padhye, Subhash
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2013, 23 (10) : 3101 - 3104