The author of 《Synthesis of trifluoromethylthiolated pyridinones through the copper-mediated trifluoromethylthiolation of iodopyridinones》 were Luo, Beibei; Zhang, Yunxiao; You, Yi; Weng, Zhiqiang. And the article was published in Organic & Biomolecular Chemistry in 2016. Synthetic Route of C6H6INO The author mentioned the following in the article:
An operationally simple method for the copper-mediated trifluoromethylthiolation of iodopyridinones employing (bpy)CuSCF3 (bpy = 2,2′-bipyridine) as a trifluoromethylthiolating reagent was presented. Various types of iodopyridinones were applicable and the trifluoromethylthiolated pyridinones were obtained in moderate to excellent yields. This method tolerated a variety of protecting groups on the nitrogen atom of pyridinones. In addition, scalability of the reaction was demonstrated. The results came from multiple reactions, including the reaction of 4-Iodo-1-methylpyridin-2(1H)-one(cas: 889865-47-8Synthetic Route of C6H6INO)
4-Iodo-1-methylpyridin-2(1H)-one(cas: 889865-47-8) belongs to organic iodides. Organic iodides are used in veterinary products (Organic Iodide Powder) as a nutritional source of iodine. In the chemical industry, alkyl iodides serve as excellent alkylating agents and, specifically, methyl iodide is used as a methylating agent in the synthesis of various pharmaceutical drugs.Synthetic Route of C6H6INO
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com