Academic–Industrial Collaboration in Synthesis with Real-Time Impact in Medicinal Chemistry: Discovery of Cystic Fibrosis C2 Corrector ABBV-602
Year: 2025
Type: review
Abstract: This article highlights synergistic real-time interactions between academic and industrial groups that drove innovations in both medicinal chemistry and catalysis. An AbbVie medicinal chemistry team had identified a promising series of trisubstituted cyclopropanes during a drug discovery campaign focused on developing CFTR C2 correctors for the treatment of cystic fibrosis. However, this unique chemical space was challenging to efficiently explore due to known limitations with previously established cyclopropanation reaction conditions. By expanding upon an existing precompetitive relationship with the Davies group at Emory University who are pioneers in development of methods for highly diastereo- and enantioselective cyclopropanations, a joint industry-academia team collaborated to discover a unique catalyst-additive system for this challenging transformation that had a broad and pharmaceutically relevant substrate scope. The optimized method was immediately applied to accelerate medicinal chemistry progress in the series, leading to the identification of novel CFTR corrector ABBV-602. Finally, a flow procedure was developed for generating the carbene precursor which enabled the reaction to be carried out on kilogram scale.
Source: ACS Medicinal Chemistry Letters
Institutions: AbbVie (United States), Emory University
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
OpenAlex ID: W4415127050
