Solvent Sustainability in Drug Discovery: Where Are We Now, and How Can We Improve?

Solvent selection plays a critical role in promoting synthetic chemistry reactions. Metrics from the ACS-GCIPR have led to an estimate that solvents utilized contribute 80-90% of the waste streams of pharmaceutical manufacturing processes. The medicinal chemistry team of the ACS-GCIPR has performed a systematic study of the most common transformations (over 400k reactions) utilized in the drug discovery phase examining the solvents in which these reactions are performed. Specifically, we have focused on the use of several solvents that are undesirable based on their hazardous nature and/or known adverse effects on human health. The data have shown that in over 40% of cases, the reactions profiled are conducted in what is an undesirable solvent with the use of methylene chloride and <i>N</i>,<i>N</i>-dimethylformamide being particularly prevalent. The perspective further discusses strategies and resources available to medicinal chemists to enable the selection of more sustainable reaction media.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-12-08
DOI
https://doi.org/10.1021/acs.jmedchem.5c01220
Citations
3
Primary Topic
Chemistry and Chemical Engineering
Type
article
Field-Weighted Citation Impact
2.58
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article

Solvent Sustainability in Drug Discovery: Where Are We Now, and How Can We Improve?

Paul Richardson, Scott Plummer, Jason Shields, Shazia Keily et al.
3 citations
Journal of Medicinal Chemistry
Chemistry and Chemical Engineering
2.58
article

Solvent Sustainability in Drug Discovery: Where Are We Now, and How Can We Improve?

Paul Richardson, Scott Plummer, Jason Shields, Shazia Keily, Anthony B. Reed, Isamir Martínez, Louis J. Diorazio, Fabrice Gallou, Charles S. Yeung, Robert J. Sheppard, Marian C. Bryan, Gail L. Wrigley, Álvaro Enríquez-García
article en
3 citations

Abstract

Solvent selection plays a critical role in promoting synthetic chemistry reactions. Metrics from the ACS-GCIPR have led to an estimate that solvents utilized contribute 80-90% of the waste streams of pharmaceutical manufacturing processes. The medicinal chemistry team of the ACS-GCIPR has performed a systematic study of the most common transformations (over 400k reactions) utilized in the drug discovery phase examining the solvents in which these reactions are performed. Specifically, we have focused on the use of several solvents that are undesirable based on their hazardous nature and/or known adverse effects on human health. The data have shown that in over 40% of cases, the reactions profiled are conducted in what is an undesirable solvent with the use of methylene chloride and <i>N</i>,<i>N</i>-dimethylformamide being particularly prevalent. The perspective further discusses strategies and resources available to medicinal chemists to enable the selection of more sustainable reaction media.

Journal of Medicinal ChemistryVol. 68(24)
AstraZeneca (United Kingdom) (GB), Novartis (Switzerland) (CH), Merck & Co., Inc., Rahway, NJ, USA (United States) (US), Amgen (United States) (US), Johnson & Johnson (United States) (US), Pfizer (United States) (US), American Chemical Society (US), Novartis (China) (CN), AstraZeneca (South Korea) (KR), Research & Development Establishment (Engrs.) (IN), AstraZeneca (Netherlands) (NL), AstraZeneca (Singapore) (SG), AstraZeneca (Brazil) (BR), Université Bourgogne Franche-Comté (FR), Vertex Pharmaceuticals (United Kingdom) (GB), Eli Lilly (Spain) (ES), Pharmaceutical Product Development (India) (IN), AstraZeneca (Poland) (PL), AstraZeneca (Sweden) (SE), AstraZeneca (United States) (US)
Openalex Percentile: Top 10%
Chemistry and Chemical Engineering
2.58
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