Die Umsetzung von 2‐Imino‐3‐aryl‐4‐oxo‐thiazolidinen (I) mit Formaldehyd (II) und den cyclischen Aminen (III) führt zu den Mannich‐Basen (IV) bzw. (VI).
Die Reaktion des Anhydrids (I) (aus Monochloressigsäure und Keten) mit Thiosemicarbazid (II) (als Hydrochlorid) liefert exotherm das Hydrazonothiazolidinon (III).
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