4.6 Article

Copper(II)-catalyzed remote sulfonylation of aminoquinolines with sodium sulfinates via radical coupling

Journal

RSC ADVANCES
Volume 6, Issue 43, Pages 37173-37179

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ra04013f

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Funding

  1. National Natural Science Foundation of China [21376058, 21302171]
  2. Zhejiang Provincial Natural Science Foundation of China [LZ13B020001]
  3. Science Technology Plan of Zhejiang Province [2014C31153]
  4. Science Technology Plan of Shandong Provincial [2012GSF11812]

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The efficient remote sulfonylation of N-(quinolin-8-yl)benzamide derivatives at the C5 position has been well developed. The reaction generates environmentally benign byproducts by utilizing stable and safe sodium sulfinates as sulfide sources. A series of N-(5-(phenylsulfonyl) quinolin-8-yl) benzamide derivatives were successfully obtained in moderate to high yields. In particular, they are less unpleasantly odorous and more environmentally friendly than previous means.

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