A sustainable strategy for the synthesis of bis-2-iminothiazolidin-4-ones utilizing novel series of asymmetrically substituted bis-thioureas as viable precursors.

ABSTRACT: A novel series of asymmetrically substituted bis-thioureas has been synthesized in an effective pattern via the reaction of diamines with isothiocyanates utilizing the ultrasonic irradiation as a sustainable energy source. This reaction performs well at mild conditions to give the products in quantitative yields for a broad scope of substrates. The bis-thiourea derivatives are used for the design of unprecedented series of bis-2-iminothiazolidin-4-ones promoted by the ultrasonic irradiation. The reaction affords the formation of regioselective products, which depends on the pK _as of the diamines. The diamine linked to the thiourea possessing lower pK _a is involved in the imino part, and the diamine having higher pK _a is a part of

SUBMITTER: Ahmed Arafa WA 

PROVIDER: S-EPMC9078912 | biostudies-literature | 2018 Mar

REPOSITORIES: biostudies-literature