Citation: Wang Tao, Xie Zhongpao, Zeng Ming, Cui Dongmei. Advances in the Synthesis of Nitrogen Zole s-Triazine Compounds[J]. Chinese Journal of Organic Chemistry, ;2018, 38(5): 983-998. doi: 10.6023/cjoc201711046 shu

Advances in the Synthesis of Nitrogen Zole s-Triazine Compounds

College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014

Corresponding author: Cui Dongmei, cuidongmei@zjut.edu.cn
Received Date: 28 November 2017
Revised Date: 8 January 2018
Available Online: 26 May 2018

Figures(36)

Nitrogen zole s-triazine derivatives display several biological activities such as antiproliferative, antioxidant, antiviral, antitumor and so on. Accordingly, much effort has been made towards the development of diverse synthetic methods for nitrogen zole s-triazines. The advancements in synthesis of nitrogen zole s-triazine compounds are summarized, including tetrazolo-s-triazines, triazolo-s-triazines and diazolo-s-triazines. At last the disadvantages of these synthetic methods are discussed and prospected to the future development.
- nitrogen zole,
- s-triazine,
- tetrazolo-s-triazine,
- triazolo-s-triazine,
- diazolo-s-triazine
1. [1]
  Wang, G.-R.; Zeng, H.-P. Chin. J. Org. Chem. 2009, 29, 1115(in Chinese).
2. [2]
  Charoensirisomboon, P.; Saito, H.; Inoue, T.; Oishi, Y.; Mori, K. Polymer 1998, 39, 2089. doi: 10.1016/S0032-3861(97)00530-2
3. [3]
4. [4]
  El, F. A.; Soliman, S. M.; Ghabbour, H. A.; Elnakady, Y. A.; Mohaya, T. A.; Siddiqui, M. R. H.; Albericio, F. J. Mol. Struct. 2016, 1125, 121. doi: 10.1016/j.molstruc.2016.06.061
5. [5]
  Bekircan, O.; Küxük, M.; Kahveci, B.; Kolaylı, S. Arch. Pharm. Chem. Life Sci. 2005, 338, 365. doi: 10.1002/(ISSN)1521-4184
6. [6]
  Bera, H.; Tan, B. J.; Sun, L. Y.; Dolzhenko, A. V.; Chui, W. K.; Chiu, G. N. C. Eur. J. Med. Chem. 2013, 67, 325. doi: 10.1016/j.ejmech.2013.06.051
7. [7]
  (a) Federico, S. ; Paoletta, S. ; Cheong, S. L. ; Pastorin, G. ; Cacciari, B. ; Stragliotto, S. ; Klotz, K. N. ; Siegel, J. ; Gao, Z. G. ; Jacobson, K. A. ; Moro, S. ; Spalluto, G. J. Med. Chem. 2011, 54, 877.
  (b) Pastorin, G. ; Federico, S. ; Paoletta, S. ; Corradino, M. ; Cateni, F. ; Cacciari, B. ; Klotz, K. N. ; Gao, Z. G. ; Jacobson, K. A. ; Spalluto, G. ; Moro, S. Bioorg. Med. Chem. 2010, 18, 2524.
  (c) Jörg, M. ; May, L. T. ; Mak, F. S. ; Lee, K. C. K. ; Miller, N. D. ; Scammells, P. J. ; Capuano, B. J. Med. Chem. 2015, 58, 718.
  (d) Jörg, M. ; Shonberg, J. ; Mak, F. S. ; Miller, N. D. ; Elizabeth, Y. ; Scammells, P. J. ; Capuano, B. Bioorg. Med. Chem. 2013, 23, 3427.
  (e) Federico, S. ; Antonella, C. ; Porta, N. ; Redenti, S. ; Pastorin, G. ; Cacciari, B. ; Klotz, K. N. ; Moro, S. ; Spalluto, G. Eur. J. Med. Chem. 2016, 108, 529.
8. [8]
  (a) Bera, H. ; Chui, W. K. ; Gupta, S. D. ; Dolzhenko, A. V. ; Sun, L. Y. Med. Chem. Res. 2013, 22, 6010.
  (b) Bera, H. ; Lee, M. H. ; Sun, L. Y. ; Dolzhenko, A. V. ; Chui, W. K. Bioorg. Chem. 2013, 50, 34.
9. [9]
  Golankiewicz, B.; Januszczyk, P.; Ikeda, S.; Balzarini, J.; Clercq, E. D. J. Med. Chem. 1995, 38, 3558. doi: 10.1021/jm00018a015
10. [10]
11. [11]
  Nie, Z.; Perretta, C.; Erickson, P.; Margosiak, S.; Lu, J.; Averill, A.; Almassy, R.; Chu, S. S. Bioorg. Med. Chem. Lett. 2008, 18, 619. doi: 10.1016/j.bmcl.2007.11.074
12. [12]
  Popowycz, F.; Schneider, C.; DeBonis, S.; Skoufias, D. A.; Kozielski, F.; Galmarini, C. M.; Joseph, B. Bioorg. Med. Chem. 2009, 17, 3471. doi: 10.1016/j.bmc.2009.03.007
13. [13]
  (a) Raboisson, P. ; Schultz, D. ; Muller, C. ; Reimund, J. Marie. ; Pinna, G. ; Mathieu, R. ; Bernard, P. ; Do, Q. T. ; DesJarlais. R. L. ; Justiano, H. ; Lugnier, C. ; Bourguignon, J. J. Eur. J. Med. Chem. 2008, 43, 816.
  (b) Nie, Z. ; Perretta, C. ; Erickson, P. ; Margosiak, S. ; Almassy, R. ; Lu, J. ; Averill, A. ; Yagera, K. M. ; Chua, S. S. Bioorg. Med. Chem. Lett. 2007, 17, 4191.
  (c) Sun, L. Y. ; Bera, H. ; Chui, W. K. Eur. J. Med. Chem. 2013, 65, 1.
  (d) Laufer, R. ; Li, S. Wan. ; Liu, Y. ; Ng, G. ; Lang, Y. H. ; Feher, M. ; Brokx, R. ; Beletskaya, I. ; Hodgson, R. ; Mao, G. D. ; Plotnikova, O. ; Awrey, D. E. ; Mason, J. M. ; Wei, X. ; Lin, D. C. C. ; Che, Y. ; Kiarash, R. ; Madeira, B. ; Fletcher, G. C. ; Mak, T. W. ; Bray, M. R. ; Pauls, H. W. Bioorg. Med. Chem. Lett. 2016, 26, 3562.
  (e) Senga, K. ; O'Brien, D. E. ; Scholten, M. B. ; Novinson, T. ; Miller, J. P. ; Robins, R. K. J. Med. Chem. 1982, 25, 243.
14. [14]
15. [15]
  Hafez, E. A. A.; Elmoghayar, M. R. H.; Ramiz, M. M. M. Liebigs Ann. Chem. 1987, 65.
16. [16]
  Kessenich, E.; Polborn, K.; Schulz, A. Inorg. Chem. 2001, 40, 1102. doi: 10.1021/ic000526k
17. [17]
  Chapyshev, S. V.; Chernyak, A. V.; Yakushchenko, I. K. J. Heterocycl. Chem. 2016, 53, 970. doi: 10.1002/jhet.v53.3
18. [18]
  Fedorov, B. S.; Fadeev, M. A.; Gidaspov, A. A.; Kosareva, E. A.; Bakharev, V. V. Chem. Heterocycl. Compd. 2005, 41, 228. doi: 10.1007/s10593-005-0132-5
19. [19]
  Bakharev, V. V.; Ghidaspov, A. A.; Krivolapov, D. B.; Mironova, E. V.; Litvinov, I. A. Chem. Heterocycl. Compd. 2006, 42, 1051. doi: 10.1007/s10593-006-0203-2
20. [20]
  Parfenov, V. E.; Bakharev, V. V.; Zavodskaya, A. V.; Selezneva, E. V.; Gidaspov, A. A.; Suponitsky, K. Y. Tetrahedron Lett. 2014, 55, 7072. doi: 10.1016/j.tetlet.2014.10.143
21. [21]
  Bokaldere, R. P.; Grinshtein, V. Y. Khim. Geterotsikl. Soedin. 1970, 6, 563.
22. [22]
  Dolzhenko, A. V.; Dolzhenko, A. V.; Chui, W. K. Tetrahedron 2007, 63, 12888. doi: 10.1016/j.tet.2007.10.046
23. [23]
  Taylor, E. C.; Hendess, R. W. J. Am. Chem. Soc. 1965, 87, 1980. doi: 10.1021/ja01087a022
24. [24]
  Evers, R.; Fischer, E. J. Prakt. Chem. 1985, 327, 609. doi: 10.1002/(ISSN)1521-3897
25. [25]
  Dorokhov, V. A.; Amamchyan, A. R.; Bogdanov, V. S. Izv. Akad. Nauk SSSR, Ser. Khim. 1989, 2386.
26. [26]
  Dorokhov, V. A.; Amamchyan, A. R.; Bogdanov, V. S.; Ugrak, B. I. Izv. Akad. Nauk SSSR, Ser. Khim. 1991, 241.
27. [27]
28. [28]
  Kalinin, D. V.; Kalinina, S. A.; Dolzhenko, A. V. Heterocycles 2012, 85, 2515. doi: 10.3987/COM-12-12542
29. [29]
  Kalinin, D. V.; Kalinina, S. A.; Dolzhenko, A. V. Heterocycles 2013, 87, 147. doi: 10.3987/COM-12-12601
30. [30]
  Zohdi, H. F. J. Chem. Res., Synop. 1998, 536.
31. [31]
  Dolzhenko, A. V.; Tan, B. J.; Dolzhenko, A. V.; Chiu, G. N. C.; Chui, W. K. J. Fluorine Chem. 2008, 129, 429. doi: 10.1016/j.jfluchem.2008.02.007
32. [32]
  Lalezari, I.; Nabahi, S. J. Heterocycl. Chem. 1980, 17, 1121. doi: 10.1002/jhet.v17:5
33. [33]
  Akahoshi, F.; Takeda, S.; Okada, T.; Kajii, M.; Nishimura, H.; Sugiura, M.; Inoue, Y.; Fukaya, C.; Naito, Y.; Imagawa, T.; Nakamura, N. J. Med. Chem. 1998, 41, 2985. doi: 10.1021/jm970759u
34. [34]
  Bereczm, G.; Pongó, L.; Kövesdi, I.; Reiter, J. J. Heterocycl. Chem. 2002, 39, 327. doi: 10.1002/jhet.5570090116
35. [35]
  Hirata, T.; Twanmoh, L. M.; Wood, H. R.; Jr.; Goldin, A.; Driscoll, J. S. J. Heterocycl. Chem. 1972, 9, 99. doi: 10.1002/jhet.5570100210
36. [36]
  Hirata, T.; Wood, H. B.; Driscoll, J. S. J. Chem. Soc., Perkin Trans. 1 1973, 1209.
37. [37]
  Okide, G. B. J. Heterocycl. Chem. 1994, 31, 535. doi: 10.1002/jhet.v31:2
38. [38]
  Kaddachi, M. T.; Zouari, S.; Benammar, H.; Cossy, J.; Kahn, P. J. Soc. Chim. Tunis. 2001, 4, 1171.
39. [39]
  Demidchuk, B. A.; Brovarets, V. S.; Chernega, A. N.; Howard, J. A. K.; Vasilenko, A. N.; Turov, A. V.; Drach, B. S. Russ. J. Gen. Chem. 2007, 77, 474. doi: 10.1134/S107036320703022X
40. [40]
  Zamigailo, L. L.; Petrova, O. N.; Shirobokova, M. G.; Lipson, V. V. Russ. J. Org. Chem. 2013, 49, 288. doi: 10.1134/S1070428013020188
41. [41]
  Fronabarger, J. W.; Chapman, R. D.; Gilardi, R. D. Tetrahedron Lett. 2006, 47, 7707. doi: 10.1016/j.tetlet.2006.08.106
42. [42]
  Khankischpur, M.; Hansen, F. K.; Geffken, D. Synthesis 2010, 1645.
43. [43]
  Dolzhenko, A. V.; Kalinina, S. A.; Kalinin, D. V. RSC Adv. 2013, 3, 15850. doi: 10.1039/c3ra41932k
44. [44]
  Tartakovsky, V. A.; Frumkin, A. E.; Churakov, A. M.; Strelenko, Y. A. Russ. Chem. Bull. 2005, 54, 719. doi: 10.1007/s11172-005-0310-8
45. [45]
  Bakharev, V. V.; Parfenov, V. E.; Ul'yankin, I. V.; Zavodskaya, A. V.; Selezneva, E. V.; Gidaspov, A. A.; Eltsov, O. S.; Slepukhin, P. A. Tetrahedron 2014, 70, 6825. doi: 10.1016/j.tet.2014.07.058
46. [46]
  Zavodskaya, A. V.; Bakharev, V. V.; Parfenov, V. E.; Gidaspov, A. A.; Slepukhin, P. A.; Isenov, M. L.; Eltsov, O. S. Tetrahedron Lett. 2015, 56, 1103. doi: 10.1016/j.tetlet.2015.01.151
47. [47]
  Bakharev, V. V.; Parfenov, V. E.; Ul'yankina, I. V.; Zavodskaya, A. V.; Gidaspov, A. A.; Slepukhin, P. A.; Chem. Heterocycl. Compd. 2015, 51, 1014. doi: 10.1007/s10593-016-1812-z
48. [48]
  Miyamoto, Y.; Yamazaki, C.; Matzui, M. J. Heterocycl. Chem. 1990, 27, 1553. doi: 10.1002/jhet.v27:6
49. [49]
  Miyamoto, Y. J. Heterocycl. Chem. 2000, 37, 1587. doi: 10.1002/jhet.v37:6
50. [50]
  Deshpande, R. J.; Roa, A. V. R. Synthesis 1974, 863.
51. [51]
  Koppes, W. M.; Sitzmann, M. E. US 6423844, 2002.
52. [52]
  Golovina, O. V.; Bakharev, V. V.; Golovin, E. V.; Parfenov, V. E.; Slepukhin, P. A. Tetrahedron Lett. 2013, 54, 3858. doi: 10.1016/j.tetlet.2013.05.052
53. [53]
  Dandia, A.; Arya, K.; Sati, M. Synth. Commun. 2004, 34, 1141. doi: 10.1081/SCC-120028646
54. [54]
  Karanik, M.; P tzel, M.; Liebscher, J. Synthesis 2003, 1201.
55. [55]
  Klein, R. S.; De, L. H.; Federico, G.; Tam, S. Y. K.; Wempen, I.; Fox, J. J. J. Heterocycl. Chem. 1976, 13, 589. doi: 10.1002/jhet.5570130333
56. [56]
  Oakes, F. T.; Leonard, N. J. J. Org. Chem. 1985, 50, 4986. doi: 10.1021/jo00224a074
57. [57]
  Lalezari, I.; Nabahi, S. J. Heterocycl. Chem. 1980, 17, 1121. doi: 10.1002/jhet.v17:5
58. [58]
  Furukawa, M.; Kawanabe, K.; Yoshimi, A.; Okawara, T.; Noguchi, Y. Chem. Pharm. Bull. 1983, 31, 2473. doi: 10.1248/cpb.31.2473
59. [59]
  Badawey, E. A. M.; Kappe, T. Arch. Pharm. Pharm. Med. Chem. 1997, 330, 59. doi: 10.1002/(ISSN)1521-4184
60. [60]
  Dolzhenko, A. V.; Chui, W. K.; Dolzhenko, A. V. Synthesis 2006, 597.
61. [61]
  Suvorova, E. Y.; Vikrishchuk, N. I.; Popov, L. D.; Starikova, Z. A.; Vikrishchuk, A. D.; Zhdanov, Y. A. Russ. J. Org. Chem. 2007, 43, 1553. doi: 10.1134/S1070428007100259
62. [62]
  Esmaeili, N.; Neshati, J.; Yavari, I. Res. Chem. Intermed. 2016, 42, 5339. doi: 10.1007/s11164-015-2369-7
63. [63]
  Kobe, J.; Stanovnik, B.; Tisler, M. Chem. Commun. (London) 1968, 1456.
64. [64]
  Dao, P.; Smith, N.; Tomkiewicz, R. C.; Yen, P. E.; Camacho, A. M.; Lietha, D.; Herbeuval, J. P.; Coumoul, X.; Garbay, C.; Chen, H. X. J. Med. Chem. 2015, 58, 237. doi: 10.1021/jm500784e
65. [65]
  Nair, V.; Lyons, A. G.; Purdy, D. F. Tetrahedron 1991, 47, 8949. doi: 10.1016/S0040-4020(01)86501-7
66. [66]
  Dao, P.; Garbay, C.; Chen, H. X. Tetrahedron 2013, 69, 3867. doi: 10.1016/j.tet.2013.03.039
67. [67]
  Voegel, J. J.; Altorfer, M. M.; Benner, S. A. Helv. Chim. Acta 1993, 76, 2061. doi: 10.1002/(ISSN)1522-2675
68. [68]
  Rao, P.; Benner, S. A. J. Org. Chem. 2001, 66, 5012. doi: 10.1021/jo005743h
69. [69]
  Li, J. J.; Song, C.; Cui, D. Mei.; Zhang, C. Org. Biomol. Chem. 2017, 15, 5564. doi: 10.1039/C7OB01018D
70. [70]
  Holtwick, J. B.; Golankiewicz, B.; Holmes, B. N.; Leonard, N. J. J. Org. Chem. 1979, 44, 3858. doi: 10.1021/jo01336a023
71. [71]
  Hosmane, R. S.; Bakthavachalam, V.; Leonard, N. J. J. Am. Chem. Soc. 1982, 104, 235. doi: 10.1021/ja00365a043
72. [72]
  Balicki, R.; Hosmane, R. S.; Leonard, N. J. J. Org. Chem. 1983, 48, 3. doi: 10.1021/jo00149a002
73. [73]
  Wang, Z. J.; Huynh, H. K.; Han, B.; Krishnamurthy, R.; Eschenmoser, A. Org. Lett. 2003, 5, 2067. doi: 10.1021/ol030044n
74. [74]
  Han, B.; Jaun, B.; Krishnamurthy, R.; Eschenmoser, A. Org. Lett. 2004, 6, 3691. doi: 10.1021/ol048649m
75. [75]
  Wagner, T.; Han, B.; Koch, G.; Krishnamurthy, R.; Eschenmoser, A. Helv. Chim. Acta 2005, 88, 1960. doi: 10.1002/(ISSN)1522-2675
76. [76]
  Novinson, T.; Senga, K.; Kobe, J.; Robins, R. K.; O'Brien, D. E.; Albert, A. A. J. Heterocycl. Chem. 1974, 11, 691. doi: 10.1002/jhet.v11:5
77. [77]
  Brandt, T. A.; Caron, S.; Damon, D. B.; DiBrino, J.; Ghosh, A.; Griffith, D. A.; Kedia, S.; Ragan, J. A.; Rose, P. R.; Vanderplas, B. C.; Wei, L. L. Tetrahedron 2009, 65, 3292. doi: 10.1016/j.tet.2008.10.067
78. [78]
  Strohmeyer, T. W.; Sliskovic, D. R.; Lang, S. A.; Jr.; Lin, Y. J. Heterocycl. Chem. 1985, 22, 7. doi: 10.1002/jhet.v22:1
79. [79]
  Insuasty, H.; Estrada, M.; Corte's, E.; Quiroga, J.; Insuasty, B.; Abonı'a, R.; Nogueras, M.; Cobo, J. Tetrahedron Lett. 2006, 47, 5441. doi: 10.1016/j.tetlet.2006.05.168
80. [80]
  Lim, F. P. L.; Luna, G.; Dolzhenko, A. V. Tetrahedron Lett. 2014, 55, 5159. doi: 10.1016/j.tetlet.2014.07.105
81. [81]
  Norman, R. E.; Perkins, M. V.; Liepa, A. J.; Francis, C. L. Aust. J. Chem. 2016, 69, 61.
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