DOI QR코드

DOI QR Code

Electron Impact Ionization Mass Spectra of 3-Substituted-2-hydroxy-4(3H)-quinazolinones

  • El Deen, I.M. (Faculty of Education, Suez Canal University) ;
  • Abd El Fattah, M.E. (Faculty of Science, Suez Canal University)
  • Published : 2003.04.20

Abstract

3-Amino-2-hydroxy-4(3H)-quinazolinone (3) was prepared via condensation of 1 with hydrazine hydrate. Treatment of 3 with appropriate acid in $POCl_3$, ethyl chloroacetate and activated olefinic compounds in DMF yielded the corresponding 3-(substituted)amino-2-hydroxy-4(3H)-quinazolinones 4, 5 and 6. The electron impact ionization mass spectra of compounds 3 and 4 show a weak molecular ion peak and a base peak of m/z 146 resulting from a cleavage fragmentation. The compounds 5 and 6 give a characteristic fragmentation pattern with a very stable fragment of benzopyrazolone (m/z 132).

Keywords

References

  1. El-Deen, I. M. J. Serb. Chem. Soc. 1998, 93(12), 915.
  2. Papudopoulos, E. P.; Torres, C. D. J. Heterocyclic Chem. 1982, 19, 269. https://doi.org/10.1002/jhet.5570190209
  3. El-Desuky, S.; El-Deen, I. M. J. Serb. Chem. Soc. 1992, 57, 513.
  4. El-Deen, I. M.; Mohamed, S. M. Indian J. Heterocycl. Chem. 1993, 2, 233
  5. Chem. Abstr. 1994, 120, 298578
  6. El-Deen, I. M.; Mohamed, S. M.; Ismail, M. M.; Abdel-Megid,M. An. Quim. 1993, 89, 621
  7. Chem. Abstr. 1994, 120, 323471
  8. Mohamed, E. A.; El-Deen, I. M.; Ismail, M. M. Pak. J. Ind. Res.1992, 2, 1427
  9. Chem. Abstr. 1993, 119, 8778
  10. Mohamed, E. A.; El-Deen, I. M.; Ismail, M. M.; Mohamed, S. M.Indian J. Chem. 1993, 32, 933
  11. Chem. Abstr. 1994, 120, 244927
  12. Abd El-Fattah, M. E. Indian J. Heterocycl. Chem. 1995, 4, 199
  13. Chem. Abstr. 1995, 132, 83306

Cited by

  1. Synthesis and mass spectral fragmentation patterns of some nitrogen heterocycles with antimicrobial activity vol.40, pp.2, 2014, https://doi.org/10.1007/s11164-012-1009-8