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Substituted 4-amino-1,2,4-triazol-3-ones were synthesized from aldehyde hydrazones and azodicarboxylates in the presence of triphenylphosphine. The cascade reaction was conducted in a single step and the procedure is general and efficient.
Substituted triazolinones were prepared by a three-component reaction of aldehydes, hydrazines and azodicarboxylates using TFA as a catalyst. The procedure was convenient and efficient, utilizing readily available substrates. A plausible mechanism for the cascade process is proposed.
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