Early Development of Ibuzatrelvir: Navigating Polymorph and Crystallization Challenges in a Protecting Group-Free Direct Amidation and Amidation-Dehydration Sequence

Abstract Ibuzatrelvir is an orally bioavailable, next-generation clinical candidate developed for the treatment of COVID-19 infections. It was identified during the pandemic, prior to the approval of PAXLOVID, and displays a more favorable pharmacokinetic profile than nirmatrelvir. Consequently, the initial development of ibuzatrelvir proceeded under highly accelerated timelines. This report details the optimization of the end-stage synthesis sequence and its advancement throughout the initial clinical production campaigns. The study highlights an efficient protecting group-free amidation of tert-leucine and describes a complex isolation process following a telescoped amidation-dehydration cascade leading to ibuzatrelvir with a 30% increase in yield. The finalized synthetic route was successfully scaled up, enabling the manufacture of several hundred kilograms to support clinical research initiatives.

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Publication Details

Journal
Organic Process Research & Development
Published
2026-09-11
DOI
https://doi.org/10.1021/acs.oprd.6c00128
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Early Development of Ibuzatrelvir: Navigating Polymorph and Crystallization Challenges in a Protecting Group-Free Direct Amidation and Amidation-Dehydration Sequence

Yiyang Liu, Johnny W. Lee, Christophe Allais, Emily Lennert et al.
Organic Process Research & Development
Chemical Synthesis and Analysis
article

Early Development of Ibuzatrelvir: Navigating Polymorph and Crystallization Challenges in a Protecting Group-Free Direct Amidation and Amidation-Dehydration Sequence

Yiyang Liu, Johnny W. Lee, Christophe Allais, Emily Lennert, Rebecca B. Watson, Aining Wang, Chintelle James, Aaron F. Baldwin, Giselle P. Reyes, María González‐Esguevillas, Yanfei Guan, D.W. Place, Melissa Lee, Michael Stanley, Samir A. Kulkarni, Philipp C. Roosen, Gerald A. Weisenburger, Hud Risley, Jeffrey M. Massicott, Robert J. Pearson, Jeanene E. Tickner, Pablo J. Cabrera, Nahian Khan, Asaad Nematalla
article en

Abstract

Abstract Ibuzatrelvir is an orally bioavailable, next-generation clinical candidate developed for the treatment of COVID-19 infections. It was identified during the pandemic, prior to the approval of PAXLOVID, and displays a more favorable pharmacokinetic profile than nirmatrelvir. Consequently, the initial development of ibuzatrelvir proceeded under highly accelerated timelines. This report details the optimization of the end-stage synthesis sequence and its advancement throughout the initial clinical production campaigns. The study highlights an efficient protecting group-free amidation of tert-leucine and describes a complex isolation process following a telescoped amidation-dehydration cascade leading to ibuzatrelvir with a 30% increase in yield. The finalized synthetic route was successfully scaled up, enabling the manufacture of several hundred kilograms to support clinical research initiatives.

Organic Process Research & Development
Pfizer (United States) (US)
Pfizer
Good health and well-being
Openalex Percentile: Top 18%
Chemical Synthesis and Analysis
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