Bi(TFA)3-[nbp]FeCl4: a new, efficient and reusable promoter system for the synthesis of 4(3H)-quinazolinone derivatives

Tetrahedron Letters

Volumn 47, Issue 21, 2006, Pages 3561-3564

  Khosropour, Ahmad R ^a   Mohammadpoor Baltork, Iraj ^a   Ghorbankhani, Hamid ^b  

^a UNIVERSITY OF ISFAHAN   (Iran)

^b RAZI UNIVERSITY   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; ANTHRANILIC ACID; BISMUTH DERIVATIVE; BISMUTH TRIFLUOROACETATE; FERRIC CHLORIDE; FORMIC ACID DERIVATIVE; IONIC LIQUID; IRON DERIVATIVE; QUINAZOLINONE DERIVATIVE; TRIMETHYL ORTHOFORMATE; UNCLASSIFIED DRUG;

ARTICLE; DRUG SYNTHESIS; POLYMERIZATION; ROOM TEMPERATURE;

EID: 33646070270     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.03.079     Document Type: Article

References (50)

1. Jang C.S., Fu F.Y., Wang C.Y., Huang K.C., Lu G., and Thou T.C. Science 103 (1946) 59
2. Martin T.A., Wheller A.G., Majewski R.F., and Corrigan J.R. J. Med. Chem. 7 (1964) 812
3. Kurogi Y., Inoue Y., Tsutsumi K., Nakamura S., Nagao K., Yohsitsugu H., and Tsuda Y. J. Med. Chem. 39 (1966) 1443
4. Ana B., and Boteanu S. Farmacia 19 (1971) 683
5. Dienei J.B., Dowalo F., Hoeven H.V., Bender P., and Love B. J. Med. Chem. 16 (1973) 633
6. Ravishankar C.H., Devender Rao A., Bhaskar Rao A., Malla Reddy V., and Sattur P.B. Curr. Sci. 53 (1984) 1069
7. Chandrasekhar V., Raghurama Rao A., and Malla Reddy V. Indian Drugs 3 (1986) 24
8. Naithani P.K., Palit G., Srivastava V.K., and Shankar K. Indian J. Chem. 28B (1989) 745
9. Dempcy R.O., and Skibo E.B. Bioorg. Med. Chem. Lett. 1 (1993) 39
10. Tereshima K., Shimamura H., Kawase A., Tanaka Y., Tanimura T., Kamisaki T., Ishizuka Y., and Sato M. Chem. Pharm. Bull. 43 (1995) 2021
11. Liverton N.J., Armstrong D.J., Claremon D.A., Remy D.C., Baldwin J.J., Lynch R.J., Zhang G., and Gould R. Bioorg. Med. Chem. Lett. 8 (1998) 484
12. Kobayashi S., Ueno M., Suzuki R., and Ishitani H. Tetrahedron Lett. 40 (1999) 2175
13. Gueyrard D., Gurnel V., Leoni O., Palmieri S., and Rollin P. Heterocycles 52 (2000) 827
14. Cao S.-L., Feng Y.-P., Jiang Y.-Y., Liu S.-Y., Ding G.-Y., and Li R.-T. Bioorg. Med. Chem. Lett. 15 (2005) 1915
15. Waisser K., Gregor J., Dostal H., Kunes J., Kubicova L., Klimesova V., and Kaustova J. Farmaco 56 (2001) 803
16. Kuneš J., Bazant J., Pour M., Waisser K., Šlosárek M., and Janota J. Farmaco 55 (2000) 725
17. Refaie F.M., Esmat A.Y., Abdel-Gawad S.M., Ibrahim A.M., and Mohamed M.A. Lipids Health Dis. 4 (2005) 22
18. Rabillound G., and Sillion B. J. Heterocycl. Chem. 17 (1980) 1065
19. Okabe M., and Sun R.-C. Tetrahedron 51 (1995) 1861
20. Chenard B.L., Welch W.M., Blake J.F., Butler T.W., Reinhold A., Ewing F.E., Menniti F.S., and Pagnozzi M.J. J. Med. Chem. 44 (2001) 1710
21. Connolly D.J., and Guiry P.J. Synlett (2001) 1707
22. Wang L., Xia J., Qin F., Qian C., and Sun J. Synthesis (2003) 1241
23. Xue S., McKenna J., Shineh W.-C., and Repič O. J. Org. Chem. 69 (2004) 6474
24. Abdel-Jalil R.J., Voelter W., and Saeed M. Tetrahedron Lett. 45 (2004) 3475
25. Das B., and Banerjee J. Chem. Lett. 33 (2004) 960
26. Liu J.-F., Lee J., Dalton A.M., Bi G., Yu L., Baldino C.M., McElory E., and Brown M. Tetrahedron Lett. 46 (2005) 1241
27. Tanaka K. Solvent Free Organic Synthesis (2003), Wiley-VCH, Weinheim
28. Sheldon R. Chem. Commun. (2001) 2399
29. Harjani J.R., Nara S.J., and Salunkhe M.M. Tetrahedron Lett. 43 (2002) 1127
30. Namboodiri V.V., and Varma R.S. Chem. Commun. (2002) 342
31. Harjani J.R., Nara S.J., and Salunkhe M.M. Tetrahedron Lett. 43 (2002) 1127
32. Yadav J.S., Reddy B.V.S., and Reddy J.S.S. J. Chem. Soc., Perkin Trans. 1 (2002) 2390
33. Yadav J.S., Reddy B.V.S., Baishya G., Harshavardhan S.J., Chary C.J., and Gupta M.K. Tetrahedron Lett. 46 (2005) 3569
34. Chauvin Y., Mussmann L., and Olivier H. Angew. Chem., Int. Ed. Engl. 34 (1995) 2698
35. Chauvin Y., Einloft S., and Olivier H. Ind. Eng. Chem. Res. 34 (1995) 1149
36. Mi X., Luo S., He J., and Cheng J.-P. Tetrahedron Lett. 45 (2004) 4567
37. Yadav J.S., Reddy B.V.S., Reddy P.M.K., and Gupta M.K. Tetrahedron Lett. 46 (2005) 8411
38. Mohammadpoor-Baltork I., Aliyan H., and Khosropour A.R. Tetrahedron 57 (2001) 5851
39. Mohammadpoor-Baltork I., and Khosropour A.R. Monatsh. Chem. 133 (2002) 189
40. Khosropour A.R., Khodaei M.M., and Ghozati K. Chem. Lett. 33 (2004) 304
41. Khodaei M.M., Khosropour A.R., and Kookhazadeh M. Tetrahedron Lett. 45 (2004) 1725
42. Khosropour A.R., Khodaei M.M., and Ghozati K. Russ. J. Org. Chem. (2004) 1332
43. Khodaei M.M., Khosropour A.R., and Ghozati K. J. Braz. Chem. Soc. 3B (2005) 673
44. Khosropour A.R., Khodaei M.M., and Ghozati K. Z. Naturforsch. B (2005) 572
45. Khodaei M.M., Khosropour A.R., and Kookhazadeh M. Can. J. Chem. 83 (2005) 209
46. Khosropour A.R., Khodaei M.M., and Ghozati K. Chem. Lett. 33 (2004) 1378
47. Khodaei M.M., Khosropour A.R., and Kookhazadeh M. Synlett (2004) 1980
48. Khosropour A.R., Khodaei M., Beygzadeh M., and Jokar M. Heterocycles 65 (2005) 767
49. Khodaei M., Khosropour A.R., and Jowkar M. Synthesis (2005) 1301
50. 3 (1 mmol) for 1 h at room temperature.