39676-47-6

Upstream product

• 1010-53-3 3-phenyl-2,4-thiazolidinedione 

Downstream Products

• 39676-36-3 2-(4-diphenylcarbamoylsulfanyl-2-oxo-3-phenyl-2,3-dihydro-thiazol-5-yl)-2H-quinoline-1-carboxylic acid diphenylamide 
• 39676-34-1 1-(4-diphenylcarbamoylsulfanyl-2-oxo-3-phenyl-2,3-dihydro-thiazol-5-yl)-2H-isoquinoline-2-carboxylic acid diphenylamide 
• 39676-40-9 5-acridin-9-yl-3-phenyl-4-thioxo-thiazolidin-2-one 
• 26862-77-1 benzaldehyde (2-oxo-3-phenyl-thiazolidin-4-ylidene)-hydrazone 
• 131841-96-8 5-[1-(1H-Indol-3-yl)-meth-(Z)-ylidene]-3-phenyl-4-thioxo-thiazolidin-2-one 
• 27315-54-4 5-[1-(4-Chloro-phenyl)-meth-(Z)-ylidene]-3-phenyl-4-thioxo-thiazolidin-2-one 
• 129333-03-5 5-[1-(4-Methoxy-phenyl)-meth-(Z)-ylidene]-3-phenyl-4-thioxo-thiazolidin-2-one 

Relevant academic research and scientific papers

Synthesis of some new 5-substituted-3-phenyl-4-thioxo-2-thiazolidinones and their fused thiopyrano[2,3-d[thiazole derivatives

The new 5-arylmethylene-3-phenyl-4-thioxo-2-thiazolidinone derivatives have been synthesized by condensation of ω-(4-formylphenoxy)acetophenone derivatives with 3-phenyl-4-thioxo-2-thiazolidinone, in good yields. The cycloaddition of the newly synthesized compounds to N-arylmaleimides, ethyl acrylate and ω-nitrostyrene has been studied. Under thermal reaction conditions [4+2] cycloaddition proceeds with complete site-and regioselectivity to yield the new fused thiopyrano[2,3-d]thiazole derivatives.