85063-56-5

Upstream product

• 2536-91-6 6-methylbenzothiazol-2-ylamine 
• 156-43-4 4-Ethoxyaniline 
• 583-68-6 2-bromo-p-toluidine 
• 3460-49-9 1-ethoxy-4-isothiocyanatobenzene 
• 29289-13-2 2-iodo-4-methylaniline 
• 622-59-3 1-isothiocyanato-4-methylbenzene 
• 3507-26-4 2-chloro-6-methylbenzo[d]thiazole 

Relevant academic research and scientific papers

1,10-Phenanthroline-catalyzed tandem reaction of 2-iodoanilines with isothiocyanates in water

The 1,10-phenanthroline-catalyzed tandem reaction of 2-iodoaniline with isothiocyanate in water is described, which provides an environmentally benign, efficient and simple route for the preparation of 2-aminobenzothiazoles. The present tandem process shows broad substrate scope in the absence of transition metals and phase-transfer catalysts. Copyright

Iron-catalyzed tandem reactions of 2-halobenzenamines with isothiocyanates leading to 2-aminobenzothiazoles

A highly practical method for the synthesis of 2-aminobenzothiazoles has been developed through an iron-catalyzed tandem reaction. The present tandem process allows the assembly of a wide range of 2-aminobenzothiazoles by the reactions of 2-halobenzenamin