Hodgin, G.A., Burns, M.J., Deadman, B.J. et al. (3 more authors) (2024) Reactivities of N-nitrosamines against common reagents and reaction conditions. Organic Process Research & Development. ISSN 1083-6160
Abstract
The knowledge of the reactivity of N-nitrosamines (NSAs) with common organic reagents in synthesis is essential in determining their presence in pharmaceutical products, if formed and retained during synthesis. In this study, we carried out a comprehensive survey of the Reaxys database for all reactions in which the NSA functional group is consumed. Very different reactivities for different classes of NSAs, e.g., N,N-dialkylnitrosamines and N,N-diphenylnitrosamine, were identified, suggesting substrates which should be included in any future reactivity screening. A classification of NSAs based on their reactivities, and corresponding reagents and transformations, was drawn up based on the data. Furthermore, the survey identified missing areas in the reported reactivities of NSAs with different reagents. This led to an experimental reactivity screening of 8 commercial NSAs with common synthetic reagents in the Mirabilis tool for purge assessment. The results showed Na₂S₂O₄ in 1 M aqueous NaOH at 50 °C to be highly effective at destroying NSAs without damaging other organic compounds.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2024 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0 . |
Keywords: | N-nitrosamines, reactivity, cheminformatics, impurity |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Chemistry (Leeds) > Organic Chemistry (Leeds) |
Depositing User: | Symplectic Publications |
Date Deposited: | 16 Sep 2024 10:20 |
Last Modified: | 30 Sep 2024 09:05 |
Published Version: | https://pubs.acs.org/doi/10.1021/acs.oprd.4c00217 |
Status: | Published online |
Publisher: | American Chemical Society |
Identification Number: | 10.1021/acs.oprd.4c00217 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:217208 |