Strain‐Release‐Driven Modular Synthesis of Oxetane‐Based Amide Bioisosteres: Concise, Robust and Scalable Approach

Abstract: Amide bioisoterism is a widely used strategy in drug development to fine‐tune physicochemical, pharmacokinetic, and metabolic properties, eliminate toxicity and gain intellectual property rights in uncharted chemical space. Of these, oxetane‐amines offer particularly exciting possibilities as bioisosteres, although they are less frequently investigated than warranted due to the lack of simple and widely applicable synthetic methods. Herein, we report a two‐step, practical, modular, robust, and scalable method for the construction of oxetane‐containing amide bioisosteres that relies on the readily available oxetan‐3‐one. This operationally simple procedure exploits the enhanced reactivity of the keto group of the commercially available oxetan‐3‐one to form amine‐benzotriazole intermediates, which springloaded adducts are then reacted with various aliphatic and aromatic organometallic reagents under mild conditions to afford various amino‐oxetanes in good to high yields. The simplicity and broad applicability of the method greatly facilitates the synthesis of derivatives that were previously difficult or impossible to produce. The usefulness of this method in the field medicinal chemistry was also demonstrated by eliminating the well‐known metabolic problem of ketoconazole.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Strain‐Release‐Driven Modular Synthesis of Oxetane‐Based Amide Bioisosteres: Concise, Robust and Scalable Approach ; volume:63 ; number:42 ; year:2024 ; extent:6
Angewandte Chemie / International edition. International edition ; 63, Heft 42 (2024) (gesamt 6)

Urheber
Spránitz, Péter
Sőregi, Petra
Hegedüs, Kristóf
Igriczi, Barbara
Szakács, Gergely
Jemnitz, Katalin
Szabó, Pál
Galushchak, Yarema
Mykhailiuk, Pavel K.
Soós, Tibor

DOI
10.1002/anie.202410554
URN
urn:nbn:de:101:1-2410071417108.081050228129
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
15.08.2025, 07:24 MESZ

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Beteiligte

  • Spránitz, Péter
  • Sőregi, Petra
  • Hegedüs, Kristóf
  • Igriczi, Barbara
  • Szakács, Gergely
  • Jemnitz, Katalin
  • Szabó, Pál
  • Galushchak, Yarema
  • Mykhailiuk, Pavel K.
  • Soós, Tibor

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