A Facile Synthesis of Dispiro[indole-3,2′-Pyrrolidine-3,5″-[1,3]Thiazolane] Derivatives from 2,3,5-Trisubstituted-4-Thiazolidinones via 1,3-Dipolar Cycloaddition Reaction
Free accessResearch articleFirst published online May, 2014
A Facile Synthesis of Dispiro[indole-3,2′-Pyrrolidine-3,5″-[1,3]Thiazolane] Derivatives from 2,3,5-Trisubstituted-4-Thiazolidinones via 1,3-Dipolar Cycloaddition Reaction
A series of 2″,3″,4′-triaryl-1′-methyldispiro[indole-3,2′-pyrrolidine-3′,5″-[1,3]thiazolane]-2(1H),4″-dione derivatives were successfully synthesised via a three-component 1,3-dipolar cycloaddition reaction of 2,3,5-trisubstituted-4-thiazolidinones, isatin and sarcosine in refluxing toluene. Such a strategy would provide access to a fast one-pot synthesis of spiroheterocycle in high yields.