On the mechanism of the generation of 5-oxy-2,3-dihydroimidazo[1,2-a]pyrazin-3-ones by the direct variable-temperature NMR method: a variable-temperature study

(Note: The full text of this document is currently only available in the PDF Version )

Katsunori Teranishi, Makoto Hisamatsu and Tetsuya Yamada


Abstract

The mechanism of the generation of 8-benzyl-2-(tert-butyl)-6-(p-methoxyphenyl)-5-oxy- 2,3-dihydroimidazo[1,2-a]pyrazin-3-ones 2a, 2b and 2c from 3-benzyl-2-[1-(2-trimethylsilylethoxycarbonyl)-2,2- dimethylpropylideneamino]-5-(p-methoxyphenyl)pyrazine 1 has been investigated. The structure of an unstable intermediate 4 forming 2a, 2b and 2c in the reactions has been proved to have a 2-(methoxycarbonyloxy)-2,3-dihydroimidazo[1,2-a]pyrazin-3-one ring system by the results of direct variable-temperature 1H NMR spectral analysis, low-temperature 13C NMR and 2D NMR (1H–13C COSY and COLOC) spectral analysis of the crude reaction mixture.


References

  1. For some of the leading references, see (a) I. X. M. Humphrey and T. Shiao-Chun, Photochem. Photobiol., 1995, 62, 607; (b) T. Shiao-Chun and I. X. M. Humphrey, Photochem. Photobiol., 1995, 62, 615.
  2. For some of the leading references, see K. Teranishi, M. Hisamatsu and T. Yamada, Tetrahedron Lett., 1996, 37, 8425 Search PubMed.
  3. K. Teranishi, M. Isobe, T. Yamada and T. Goto, Tetrahedron Lett., 1992, 33, 1303 CrossRef CAS.
  4. K. Teranishi, K. Ueda, M. Hisamatsu and T. Yamada, Biosci. Biotech. Biochem., 1995, 59, 104 CAS.
  5. Y. Kishi, H. Tanino and T. Goto, Tetrahedron Lett., 1972, 2747 CrossRef CAS.
  6. I. Saito, R. Nagata, K. Yuba and T. Matsuura, Tetrahedron Lett., 1983, 24, 1737 CrossRef CAS.