Organic reactions in ionic liquids. Ionic liquid-accelerated facile synthesis of 3-alkyl-2,4-thiazolidinediones was written by Yang, De-Hong;Yang, Ben-Yong;Chen, Zhen-Chu;Chen, Song-Ying;Zheng, Qin-Guo. And the article was included in Journal of Chemical Research in 2005.Application In Synthesis of 3-Methylthiazolidine-2,4-dione This article mentions the following:
The room temperature ionic liquid [bmim]PF6 is a new green solvent for the N-alkylation of 2,4-thiazolidinones. Significant rate enhancement and improved yields were observed In the experiment, the researchers used many compounds, for example, 3-Methylthiazolidine-2,4-dione (cas: 16312-21-3Application In Synthesis of 3-Methylthiazolidine-2,4-dione).
3-Methylthiazolidine-2,4-dione (cas: 16312-21-3) belongs to thiazolidine derivatives. Thiazolidine is an important scaffold and has a wide range of promising biological activities. Thiazolidine derivatives have reported anti-inflammatory and anti-nociceptive activity. Open-chain compounds are obtained when thiazolidines are treated with tris(trimethylsilyl)silane in a reaction in which the thiazolidine derivatives act as a source of α-aminoalkyl radicals.Application In Synthesis of 3-Methylthiazolidine-2,4-dione
Referemce:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com