A copy of this work was available on the public web and has been preserved in the Wayback Machine. The capture dates from 2017; you can also visit the original URL.
The file type is application/pdf
.
Synthesis and Properties of Some New 1,4-Dihydrothieno[3,2-e][1,2,4]triazepin-5-ones
2006
Zeitschrift für Naturforschung. B, A journal of chemical sciences
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.
doi:10.1515/znb-2006-0113
fatcat:kicbiqsklbekvasw7e3e7pu5ou