SBMU, Pharmaceutical Research Sciences
  • Register
  • Login
International Pharmacy Acta
  • Home
  • Journal Info
    • About
    • Aim and Scope
    • Ownership & Management
    • Indexing
    • Editorial Team
  • New Submission
  • Author Guidelines
    • Guideline
    • Types of articles
    • Templates
    • Publication Fees
  • Policies and Process
    • Publication Policy
    • Peer Review Process
    • Open Access Policy
    • plagiarism
    • Archiving
    • Privacy Statement
    • Copyright Notice
    • Waiver policy
    • Complaints Policy
    • Post- Publication Discussions and Corrections Policy
    • Advertisement and Marketing
  • Issues
    • Current
    • Archives
  • Contact us
Advanced Search
  1. Home
  2. Archives
  3. Vol. 5 No. 1 (2022)
  4. Original Research article

Vol. 5 No. 1 (2022)

June 2022

Green Synthesis of Nalidixic Acid by Ionic Liquid Using ionic liquid for drug synthesis

  • Hamid Reza Ahfad-Hosseini
  • Hasan Bagheri
  • Salimeh Amidi

International Pharmacy Acta, Vol. 5 No. 1 (2022), 19 June 2022 , Page e1:1-5
https://doi.org/10.22037/ipa.v5i1.36873 Published: 2022-06-14

  • View Article
  • Download
  • Cite
  • References
  • Statastics
  • Share

Abstract

In this study, a green process was applied for the preparation of nalidixic acid by the assistance of an ionic liquid. Nalidixic acid was prepared by reaction of 6-methylpyridin-2-amine, ethyl formate and diethyl malonate in tris-(2-hydroxyethyl) ammonium acetate solution as ionic liquid (IL) which was provided by reaction of triethanolamine and acetic acid. The 1HNMR, 13CNMR, FTIR, mass spectroscopy and melting point were used to characterize the structure of the synthesized compounds. The ionic liquid was recovered and reused for four runs. This method introduces a novel idea for synthesis of nalidixic acid with high yield (86%) and the least damage to the environment. This IL can be used as a green solvent in synthesis of compounds instead of using harmful solvents.

Keywords:
  • Nalidixic acid
  • Ionic liquid
  • Synthesis
  • PDF-2022e1

How to Cite

Ahfad-Hosseini, H. R. ., Bagheri, H., & Amidi, S. (2022). Green Synthesis of Nalidixic Acid by Ionic Liquid: Using ionic liquid for drug synthesis. International Pharmacy Acta, 5(1), e1:1–5. https://doi.org/10.22037/ipa.v5i1.36873
  • ACM
  • ACS
  • APA
  • ABNT
  • Chicago
  • Harvard
  • IEEE
  • MLA
  • Turabian
  • Vancouver
  • Endnote/Zotero/Mendeley (RIS)
  • BibTeX

References

Madaan A, Verma R, Kumar V, Singh AT, Jain SK, Jaggi M. 1,8-Naphthyridine Derivatives: A Review of Multiple Biological Activities. Arch Pharm (Weinheim). 2015;348(12):837-60.

Ahmed NS, AlFooty KO, Khalifah SS. Synthesis of 1,8-Naphthyridine Derivatives under Ultrasound Irradiation and Cytotoxic Activity against HepG2 Cell Lines. J Chem. 2014;2014:1-8.

World Health Organization. WHO model prescribing information : drugs used in bacterial infections. Geneva: World Health Organization; 2001.

Ram Singh G. Synthesis of Selected Novel Covalently Linked Flavoquinolones. Synthesis. 2005;2005(14):2315-20.

Hajimahdi Z, Zabihollahi R, Aghasadeghi MR, Ashtiani SH, Zarghi A. Novel quinolone-3-carboxylic acid derivatives as anti-HIV-1 agents: design, synthesis, and biological activities. Med Chem Res. 2016;25(9):1861-76.

Brown EV. 1, 8-Naphthyridines. I. Derivatives of 2-and 4-methyl-1, 8-naphthyridines. J Org Chem. 1965;30(5):1607-10.

Le Z-G, Liang M, Chen Z-S, Zhang S-H, Xie Z-B. Ionic Liquid as an Efficient Medium for the Synthesis of Quinoline Derivatives via α-Chymotrypsin-Catalyzed Friedländer Condensation. Molecules. 2017;22(5):762-.

Qureshi ZS, Deshmukh KM, Bhanage BM. Applications of ionic liquids in organic synthesis and catalysis. Clean Technol Environ Policy. 2014;16(8):1487-513.

Fang D, Liu Z-L. Synthesis of 14-aryl-14 H -dibenzo[ a,j ]xanthenes catalyzed by acyclic acidic ionic liquids. J Heterocycl Chem. 2010;55(5):509-12.

Du B-X, Li Y-L, Wang X-S, Shi D-Q. Ionic Liquid as an Efficient and Recyclable Reaction Medium for the Synthesis of Pyrido[2,3- d ]pyrimidines. J Heterocycl Chem. 2013;50(3):534-8.

Ratti R. Ionic Liquids: Synthesis and Applications in Catalysis. Adv Chem. 2014;2014(3):1-16.

Lei Z, Chen B, Koo YM, Macfarlane DR. Introduction: Ionic Liquids. Chem Rev. 2017;117(10):6633-5.

Alizadeh A, Khodaei MM, Eshghi A. Ambiphilic dual activation role of a task-specific ionic liquid: 2-hydroxyethylammonium formate as a recyclable promoter and medium for the green synthesis of β-nitrostyrenes. J Org Chem. 2010;75(23):8295-8.

Feng B-B, Zhang M-M, Wang X-S. Green Synthesis of Fused Polycyclic Pyrazolo[3,4-b][1,6]naphthyridine Derivatives in Ionic Liquids via Three-Component Reaction. Polycyclic Aromat Compd. 2016;36(4):478-89.

Ahfad-Hosseini HR, Bagheri H, Amidi S. Ionic liquid-assisted synthesis of celexocib using tris-(2-hydroxyethyl) ammonium acetate as an efficient and reusable catalyst. Iran J Pharm Res. 2017;16(1):158-64.

Iranpoor N, Firouzabadi H, Ahmadi Y. Carboxylate-Based, Room-Temperature Ionic Liquids as Efficient Media for Palladium-Catalyzed Homocoupling and Sonogashira–Hagihara Reactions of Aryl Halides. European J Org Chem. 2012;2012(2):305-11.

Voronkov MG, Albanov AI, Aksamentova TN, Adamovich SN, Chipanina NN, Mirskov RG, et al. Tris(2-hydroxyethyl)ammonium salts: 2,8,9-Trihydroprotatranes. Russ J Gen Chem. 2009;79(11):2339-46.

  • Abstract Viewed: 490 times
  • PDF-2022e1 Downloaded: 304 times

Download Statastics

  • Linkedin
  • Twitter
  • Facebook
  • Google Plus
  • Telegram

Information

  • For Readers
  • For Authors
  • For Librarians

Make a Submission

Make a Submission
  • Home
  • Archives
  • Submissions
  • About the Journal
  • Editorial Team
  • Contact

Creative Commons License
This journal (and its contents) is licensed under a  Creative Commons Attribution-NonCommercial 4.0 International License.

 

                                                  Online ISSN: 2645-3266

                                                  Print ISSN: 2645-3258                                                 

Powered by OJSPlus