Abstract
Functionalized aryl sulfonamides are important building blocks in the pharmaceutical industry. A one-step synthesis catalyzed by a copper salt was developed using stable solid commodity chemicals in sulfolane or, alternatively, in green solvents such as γ-valerolactone, iPrOAc, or nBuOAc with acetic acid. The method tolerated diverse functional groups commonly presented in current medicines and drug intermediates. The mechanistic study showed a radical coupling pathway between the sulfonyl and anilinium radicals through the use of K2S2O8 and copper catalyst, respectively.
Original language | English |
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Pages (from-to) | 8802-8810 |
Number of pages | 9 |
Journal | Journal of Organic Chemistry |
Volume | 87 |
Issue number | 13 |
DOIs | |
Publication status | Published - 1 Jul 2022 |