1,3-Dibromo-5,5-dimethylhydantoin (DBH) as an efficient promoter for acetylation of 3-arylsydnones in the presence of acetic anhydride under neutral conditions

Journal of Heterocyclic Chemistry

Volumn 44, Issue 2, 2007, Pages 467-469

  Azarifar, Davood ^a   Bosra, Hassan Ghasemnejad ^a   Tajbaksh, Mahmood ^b  

^a BU ALI SINA UNIVERSITY   (Iran)

^b UNIVERSITY OF MAZANDARAN   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

1,3 DIBROMO 5,5 DIMETHYLHYDANTOIN; ACETIC ANHYDRIDE; HYDANTOIN DERIVATIVE; SYDNONE DERIVATIVE; UNCLASSIFIED DRUG;

ACETYLATION; ARTICLE; SYNTHESIS;

EID: 34249941067     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570440231     Document Type: Article

References (37)

1. M. Ohta and H. Kato, In Nonbenzenoid Aromatics Vol. 1, J. P. Snyder, ed., Academic Press, Inc., New York, NY, 1969, p 146;
2. [b] F. H. C. Stewart, Chem. Rev. 64, 129 (1964).
3. 'Mesoionic compounds', W. D. Ollis and C. A. Ramsden, Adv. Heterocycl. Chem., 19, 1 (1976),
4. 'Mesoionic Heterocycles (1976-1980)', C. G. Newton and C. A. Ramsden, Tetrahedron, 38, 2965 (1982).
5. J. C. Earl and A. W. Mackney, J. Chem. Soc., 899 (1935).
6. C. J. Thoman and D. Voaden, Org. Synth., Coll. Vol . V, 962 (1973).
7. P. Brooks and J. Walker, J. Chem. Soc., 4409 (1959);
8. [b] E. Ackermann, Pharmazie, 22, 537 (1967);
9. Chem. Abstr., 68, 28171 (1968).
10. L. B. Kier and E. B. Roche, J. Pharm. Sci., 56, 149 (1967).
11. D. J. McCaustland, W. H. Burton, and C. C. Cheng, J. Heterocyclic Chem., 8, 89 (1971).
12. G. Pala, A. Mantegani, G. Coppi, and R. Genova, Chim. Ther., 4, 31 (1969);
13. Chem. Abstr., 71, 3328 (1969);
14. [b] T. Kamiya, Y. Saito, and T. Teraji, (Fujisawa Pharm. Co., Ltd.), Japan, 72 32, 073; Chem. Abstr., 78, 42592 (1973).
15. Y. Saito and T. Kamiya, (Takeda Chem. Ind. Ltd.), Japan, 70 10, 510; Chem. Abstr., 73, 14853 (1970).
16. K. Turnbull, J. Heterocyclic Chem., 22, 965 (1985).
17. R. Huisgen, R. Grashey, H. Gotthardt, and R. Schmidt, Angew. Chem., 74, 29 (1962).
18. C. Tin-Lok, J. Miller, and F. Stansfield, J. Chem. Soc., 1213 (1964).
19. K. Turnbull, T. L. Blackburn, and J. Miller, J. Heterocycl. Chem., 33, 485 (1996).
20. H.-J. Tien, J.-C. Yeh, and S.-C. Wu, J. Chin. Chem. Soc., 39, 443 (1992).
21. A. Cornelis and P. Laszlo, Synlett, 155 (1994).
22. P. Laszlo and A. Mathy, Helv. Chim. Acta, 70, 577 (1987).
23. V. F. Vasil'eva and V. G. Yashunski, Khim. Nauk Prom., 3, 282 (1958).
24. V. F. Vasil'eva and V. G. Yashunski, Dokl. Akad. Nauk SSSR, 130, 350 (1960);
25. Chem. Abstr., 54, 10999h (1960).
26. H.-J. Tien and M. Ohta, Bull. Chem. Soc. Jpn., 45, 2944 (1972).
27. H.-J. Tien, Hua Hsueh, 8 (1977);
28. Chem. Abstr. 92, 110930k (1980).
29. C. V. Greco, J. Tobias, and L. B. Kier, J. Heterocycl. Chem., 4, 160 (1967).
30. K. Turnbull and J. C. George, Synth, Commun., 26, 2757 (1996).
31. D. Azarifar, M. A. Zolfigol, and B. Maleki, Synthesis, 1744 (2004)
32. D. Azarifar, M. A. Zolfigol, and B. Maleki, Bull. Korean Chem. Soc., 25, 23 (2004).
33. D. Azarifar, H. Ghasemnejad-Bosra, and F. Ramazanian-Lehmali, Mendeleev Commun., 15, 209 (2005).
34. D. Azarifar, H. Ghasemnejad-Bosra, M. A. Zolfigol, and M. Tajbaksh, Heterocycles, 68, 175 (2006).
35. D.Azarifar and H. Ghasemnejad-Bosra, Synthesis, 1123 (2006).
36. M. A. Zolfigol, A. Khazaei, A. Ghorbani, A. Rostami, and M. Hajjami, Cataly. Commun., 7, 399 (2006).
37. H.-J. Tien, G.-M. Fang, S.-T. Lin, and L.-L. Tien, J. Chin. Chem. Soc., 38, 171 (1991).