---
_id: '61335'
abstract:
- lang: eng
  text: <jats:p>Amidines are a ubiquitous class of bioactive compounds found in a
    wide variety of natural products; thus, efficient strategies for their preparation
    are in great demand. Herein, a novel protocol is reported for the synthesis of
    amidines based on P<jats:sup>III</jats:sup>/P<jats:sup>V</jats:sup>O redox catalysis.
    This two‐step, one‐pot approach involves the activation of amides via P<jats:sup>III</jats:sup>/P<jats:sup>V</jats:sup>O
    catalyzed in situ formation of imidoyl chloride intermediates which are directly
    converted upon reaction with amines into the corresponding amidines. Instead of
    traditionally used toxic and corrosive chloride sources, hexachloroacetone (HCA)
    is successfully employed as a halide source. The reaction proceeds with low catalyst
    loading (2 mol%) in BuOAc as the solvent. Under the optimized conditions, 20 amidines
    are prepared in yields up to 99%. A feasible mechanism is proposed based on experimental
    results. The synthetic potential of this method is evaluated in the preparation
    of the tyrosine kinase inhibitor (TKI) Erlotinib.</jats:p>
article_number: '202500394'
author:
- first_name: Viktorija
  full_name: Medvaric, Viktorija
  id: '92677'
  last_name: Medvaric
- first_name: Jan
  full_name: Paradies, Jan
  id: '53339'
  last_name: Paradies
  orcid: 0000-0002-3698-668X
- first_name: Thomas
  full_name: Werner, Thomas
  id: '89271'
  last_name: Werner
  orcid: 0000-0001-9025-3244
citation:
  ama: Medvaric V, Paradies J, Werner T. Synthesis of Amidines Via P(III)/P(V)=O Redox
    Catalyzed In Situ Formation of Imidoyl Chlorides From Amides. <i>Advanced Synthesis
    and Catalysis</i>. Published online 2025. doi:<a href="https://doi.org/10.1002/adsc.70059">10.1002/adsc.70059</a>
  apa: Medvaric, V., Paradies, J., &#38; Werner, T. (2025). Synthesis of Amidines
    Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From
    Amides. <i>Advanced Synthesis and Catalysis</i>, Article 202500394. <a href="https://doi.org/10.1002/adsc.70059">https://doi.org/10.1002/adsc.70059</a>
  bibtex: '@article{Medvaric_Paradies_Werner_2025, title={Synthesis of Amidines Via
    P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides},
    DOI={<a href="https://doi.org/10.1002/adsc.70059">10.1002/adsc.70059</a>}, number={202500394},
    journal={Advanced Synthesis and Catalysis}, publisher={Wiley}, author={Medvaric,
    Viktorija and Paradies, Jan and Werner, Thomas}, year={2025} }'
  chicago: Medvaric, Viktorija, Jan Paradies, and Thomas Werner. “Synthesis of Amidines
    Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From
    Amides.” <i>Advanced Synthesis and Catalysis</i>, 2025. <a href="https://doi.org/10.1002/adsc.70059">https://doi.org/10.1002/adsc.70059</a>.
  ieee: 'V. Medvaric, J. Paradies, and T. Werner, “Synthesis of Amidines Via P(III)/P(V)=O
    Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides,” <i>Advanced
    Synthesis and Catalysis</i>, Art. no. 202500394, 2025, doi: <a href="https://doi.org/10.1002/adsc.70059">10.1002/adsc.70059</a>.'
  mla: Medvaric, Viktorija, et al. “Synthesis of Amidines Via P(III)/P(V)=O Redox
    Catalyzed In Situ Formation of Imidoyl Chlorides From Amides.” <i>Advanced Synthesis
    and Catalysis</i>, 202500394, Wiley, 2025, doi:<a href="https://doi.org/10.1002/adsc.70059">10.1002/adsc.70059</a>.
  short: V. Medvaric, J. Paradies, T. Werner, Advanced Synthesis and Catalysis (2025).
date_created: 2025-09-17T15:16:49Z
date_updated: 2025-11-10T08:44:04Z
department:
- _id: '2'
- _id: '389'
doi: 10.1002/adsc.70059
keyword:
- T2
- T
- CSSD
language:
- iso: eng
publication: Advanced Synthesis and Catalysis
publication_identifier:
  issn:
  - 1615-4150
  - 1615-4169
publication_status: published
publisher: Wiley
status: public
title: Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of
  Imidoyl Chlorides From Amides
type: journal_article
user_id: '89271'
year: '2025'
...
