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Synlett 2019; 30(05): 605-609
DOI: 10.1055/s-0037-1612077
DOI: 10.1055/s-0037-1612077
letter
One-Pot Sequential Multistep Transformation of α,β-Unsaturated Trifluoromethyl Ketones: Facile Synthesis of Trifluoromethylated 2-Pyridones
This work was supported financially by the National Natural Science Foundation of China (No. 21472137, 21532008, and 21772142) and the National Basic Research Program of China (973 Program: 2014CB745100).
Further Information
Publication History
Received: 16 October 2018
Accepted after revision: 21 December 2018
Publication Date:
23 January 2019 (online)


Abstract
A one-pot transformation of α,β-unsaturated trifluoromethyl ketones with 2-(phenylsulfinyl)acetamide to give trifluoromethylated 2-pyridones is realized. The reaction proceeds under mild conditions and involves multiple steps in an expeditious and controlled sequence to provide efficient access to a broad range of trifluoromethylated 2-pyridones in moderate to high yields. Moreover, further synthetic manipulations permit the routine synthesis of a diverse array of trifluoromethylated pyridines with good efficiency.
Key words
trifluoromethyl group - pyridones - trifluoromethylpyridines - one-pot synthesis - multistep reactionSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0037-1612077.
- Supporting Information