Synlett
DOI: 10.1055/a-2725-5792
Letter

Functionalized Diphenyl (2-Oxochroman-4-yl)phosphonates: Dual Synthetic Approaches, Mechanistic Insights, and Exploration of a Promising Anti-Lung Cancerous Molecule

Authors

  • Indrajit Karmakar

    1   Department of Chemistry, Visva-Bharati (a Central University), Santiniketan, India (Ringgold ID: RIN449338)
  • Sudipa Chatterjee

    2   Department of Biotechnology, Visva-Bharati Institute of Science, Santiniketan, India (Ringgold ID: RIN449338)
  • Souvik Das

    1   Department of Chemistry, Visva-Bharati (a Central University), Santiniketan, India (Ringgold ID: RIN449338)
  • Asanjan Brahmachari

    1   Department of Chemistry, Visva-Bharati (a Central University), Santiniketan, India (Ringgold ID: RIN449338)
  • GourabKanti Das

    1   Department of Chemistry, Visva-Bharati (a Central University), Santiniketan, India (Ringgold ID: RIN449338)
  • Tathagata Choudhuri

    2   Department of Biotechnology, Visva-Bharati Institute of Science, Santiniketan, India (Ringgold ID: RIN449338)
  • Goutam Brahmachari

    1   Department of Chemistry, Visva-Bharati (a Central University), Santiniketan, India (Ringgold ID: RIN449338)

Partial Financial support from the Science and Engineering Research Board (Grant No. CRG/2022/000275), Department of Science & Technology (DST), and the Council of Scientific and Industrial Research (Grant No. 02/00464/23/EMR-II), Government of India, New Delhi.
Supported by: Council of Scientific and Industrial Research 02/00464/23/EMR-II


Graphical Abstract

Abstract

We herein disclose a dual synthetic approach involving room temperature and mechanochemical strategies for a new series of substituted diphenyl (2-oxochroman-4-yl)phosphonates. Both methods offer a practical and straightforward synthetic route for these biorelevant organophosphorus compounds. The salient features of both methods are metal-free synthesis, mild and energy-efficient reaction conditions, good yields with high chemo- and regioselectivity, the avoidance of column chromatographic purification, gram-scale synthetic applicability, and operational simplicity. The density functional theory study provides mechanistic insights into this transformation. Furthermore, biological studies of the synthesized organophosphorus compounds explored their possible anticancer profiles, and among the series, diphenyl (6-(tert-butyl)-2-oxochroman-4-yl)phosphonate (3c) exhibited anti-lung cancer activity in vitro. We herein emphasize that 3c might be considered for preclinical evaluation to establish its therapeutic relevance as an anticancer agent.

Supporting Information

General information, synthetic methods, physical, spectroscopic, and analytical data, scanned copies of respective 1H NMR, 13C NMR, DEPT-135, 31P NMR, and 2D NMR (for one representative compound 3e) spectra for all the synthesized compounds 3a–3l, along with representative HRMS spectra for compounds 3a and 3c, are documented in the Supporting Information. Coordinates and other thermodynamic parameters of the optimized geometries obtained on the Potential Energy Surface (PES). Compound screening based on physicochemical and pharmacokinetic profiles, biological significance analysis of the identified gene set, simplified Molecular Input Line Entry Specification (SMILES) and chemical structure of the compound, physicochemical and pharmacokinetic properties of 3c and probable biological targets for compound 3c. (PDF)




Publication History

Received: 08 August 2025

Accepted after revision: 16 October 2025

Accepted Manuscript online:
16 October 2025

Article published online:
20 November 2025

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