Reactions with 2-Thiohydantoin, Synthesis of Imidazothiazolone Derivatives and Mannich Bases of 5-Arylidene-2-thiohydantoin

A. F. A. Shalaby 1 , H. A. Daboun 1  and M. A. Abdel Aziz 1
  • 1 Chemistry Department, Faculty of Science, Cairo University, Egypt

Treatment of 5-arylidene-2-thiohydantoin (1a-d) with alkyl bromoacetate and chloroacetic acid gave the esters 2a-f and the acids 2g-j, respectively. 2a was refluxed with concentrated hydrochloric acid to give 5-benzylidene hydantoin. 2 was cyclized with acetic anhydride to give the bicyclic product 3. 5-Arylidene-2-thiohydantoin derivatives (1a, b) and (8a) condense with formaldehyde and primary or secondary amines to give the corresponding Mannich bases 6a-f and 8c-e, respectively. The assigned structure 6 and 8 finds support from the chemical evidences

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Zeitschrift für Naturforschung B is an international scientific journal which publishes original papers, microreviews, and letters from all areas of inorganic chemistry, solid state chemistry, coordination chemistry, molecular chemistry, and organic chemistry.

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