Studies in quinoxaline series. Part 18. Structure of products of a new reaction of tetrazolo[1,5-a]quinoxaline 5-oxide with carbanions. X-Ray molecular structure of 4-acetyl-4-methyl-3b,4-dihydroazirino[1,2-a]tetrazolo-[5,1-c]quinoxaline

Abstract

Tetrazolo[1,5-a]quinoxaline-5-oxide 4 reacts with the carbanions of β-diketones and β-keto esters to give enaminoketones and enamino esters, respectively. The N-oxide 4 reacts with 3-methyl- and 3-ethyl-pentane-2,4-dione under similar conditions to give a racemic mixture of the derivatives of aziridinotetrazoloquinoxaline 10 and 11. Their structure and the trans configuration of hydrogen atom and methyl group on the aziridine ring of compound 10 were estimated by means of ¹H and ¹³C NMR spectroscopy, and were in accord with the results of X-ray diffraction measurements, which also provided bond lengths, and valence, torsion, and dihedral angles.