Methyl 3-aminothiophene-2-carboxylate reacts readily, in the presence of triethylamine, with hydrazonoyl chlorides (7a - c) to afford good yields of the corresponding N-arylamidrazones (8a - c). The latter acyclic adducts undergo, in the presence of t-BuOK/t-BuOH, cyclocondensation accompanied by elimination of the acetyl group present in 8, to deliver the respective thieno-1,3,4-triazepin- 5-ones 10a - c.

This study demonstrates the facile synthesis of 1,4-dihydrothieno[3,2-e][1,2,4]triazepin-5-ones using methyl 3-aminothiophene-2-carboxylate and hydrazonoyl chlorides, with promising applications in organic

Paper

Synthesis and Properties of Some New 1,4-Dihydrothieno[3,2-e][1,2,4]triazepin-5-ones

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