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Hetarylcyanamides. (Review)

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The nomenclature and the synthesis of hetarylcyanamides and their reactions that take place at the cyanoamino group are discussed.

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References

  1. P. H. Benders, D. N. Reinhoundt, and D. M. W. Ham, Rec. Trav. Chim., 100, 330 (1981).

    Google Scholar 

  2. G. Pellizzari, Chem. Zbl., 3, 527 (1921).

    Google Scholar 

  3. B. Serafin, L. Konopsky, and L. Stolarczuk, Roczn. Chem., 51, 2355 (1977).

    Google Scholar 

  4. E. A. Watts, Ger. Patent 2267312; Chem. Abstr., 79, 5332 (1973).

    Google Scholar 

  5. R. Ruegg and G. Ryser, Ger. Patent 2252805; Chem. Abstr., 19, 53325 (1973).

    Google Scholar 

  6. E. A. Watts, Brit. Patent 1408408; Chem. Abstr., 84, 17355 (1976).

    Google Scholar 

  7. L. S. Witenbrook, J. Heterocycl. Chem., 12, 37 (1975).

    Google Scholar 

  8. R. L. Webb and C. S. Labaw, J. Heterocycl. Chem., 19, 1205 (1982).

    Google Scholar 

  9. S. Birtwell, J. Chem. Soc., 1725 (1953).

  10. A. Krebs, Ger. Patent 3641827; Chem. Abstr., 109, 149570 (1988).

    Google Scholar 

  11. B. Stanovnik, A. Stimac, M. Tisler, and B. Vercek, J. Heterocycl. Chem., 19, 577 (1982).

    Google Scholar 

  12. B. Vercek, B. Ogorevc, B. Stanovnik, and M. Tisler, Vestn. Slav. Kern. Drus., 30, 51 (1983).

    Google Scholar 

  13. R. Charonnat and F. Le Perdriel, Ann. Pharm. France, 26, 469 (1968).

    Google Scholar 

  14. L. A. Khachatryan, Thesis for Candidate of Chemical Sciences [in Russian], Erevan (1983).

  15. Lonza Ltd., Brit. Patent 1052567; Chem. Abstr., 66, 55525 (1967).

    Google Scholar 

  16. H. Hintermaier, U. Maier, and M. Obinger, Ger. Patent 226082; Chem. Abstr., 81, 91582 (1974).

    Google Scholar 

  17. R. Freiberg and E. Bulka, J. Prakt. Chem., 397, 417 (1985).

    Google Scholar 

  18. H. J. Riebel, R. Fauss, and A. Krebs, Ger. Patent 3611198; Chem. Abstr., 108, 21933 (1988).

    Google Scholar 

  19. H. J. Riebel, R. Fauss, and A. Krebs, Eur. Patent 200064; Chem. Abstr., 106, 50262 (1987).

    Google Scholar 

  20. V. V. Dovlatyan, L. A. Khachatryan, and E. N. Ambartsumyan, Arm. Khim. Zh., 32, 569 (1979).

    Google Scholar 

  21. V. V. Dovlatyan and L. A. Khachatryan, USSR Inventor's Certificate 468497; Byull. Izobr., No. 5, 236 (1979).

    Google Scholar 

  22. V. V. Dovlatyan and L. A. Khachatryan, Swiss Pat. 625794; Chem. Abstr., 90, 186981 (1979).

    Google Scholar 

  23. V. V. Dovlatyan and L. A. Khachatryan, Ger. Patent 2653834; Chem. Abstr., 90, 104019 (1979).

    Google Scholar 

  24. Armenian Agricultural Institute, Jpn. Patent 7871089; Chem. Abstr., 90, 6424 (1979).

    Google Scholar 

  25. R. Fauss and H. J. Riebel, Ger. Patent 3507750; Chem. Abstr., 105, 226663 (1986).

    Google Scholar 

  26. Hitachi, Jpn. Patent 58131972; Chem. Abstr., 100, 7362 (1984).

    Google Scholar 

  27. B. Vercek, B. Stanovnik, and M. Tisler, Heterocycles, 11, 313 (1978).

    Google Scholar 

  28. B. Koren, B. Stanovnik, and M. Tisler, Heterocycles, 26, 689 (1987).

    Google Scholar 

  29. G. R. Revcencar, R. V. Robins, and R. L. Tolman, J. Org. Chem., 39, 1256 (1974).

    Google Scholar 

  30. M. Hori, K. Tanaka, T. Kataoka, H. Shimizu, E. Imai, K. Kimura, and Y. Hashimoto, Tetrahedron Lett., 1321 (1985).

  31. M. Hori, K. Tanaka, T. Kataoka, H. Shimizu, E. Imai, K. Kimura, and Y. Hashimoto, J. Chem. Soc. Perkin Trans. I, 2333 (1985).

  32. V. N. Konyukhov, L. N. Dianova, T. G. Koshkarova, N. V. Volkova, V. A. Bakulev, and O. S. Anisimova, Khim. Geterotsikl. Soedin., 421 (1985).

  33. V. V. Dovlatyan, E. N. Ambartsumyan, L. A. Khachatryan, and S. G. Bagrazyan, USSR Inventor's Certificate 448716; Byull. Izobr., No. 5, 237 (1979).

    Google Scholar 

  34. V. V. Dovlatyan, E. N. Ambartsumyan, L. A. Khachatryan, and S. G. Bagrazyan, Ger. Patent 2657944; Chem. Abstr., 90, 67719 (1979).

    Google Scholar 

  35. V. V. Dovlatyan, E. N. Ambartsumyan, L. A. Khachatryan, and S. G. Bagrazyan, Swiss Patent 605854; Chem. Abstr., 90, 67719 (1979).

    Google Scholar 

  36. V. V. Dovlatyan, L. A. Khachatryan, and E. N. Ambartsumyan, Arm. Khim. Zh., 33, 311 (1980).

    Google Scholar 

  37. V. V. Dovlatyan, L. L. Gyul'budagyan, and E. N. Ambartsumyan, Arm. Khim. Zh., 35, 478 (1982).

    Google Scholar 

  38. G. S. Amazaspyan, E. N. Ambartsumyan, and V. V. Dovlatyan, Arm. Khim. Zh., 43, 668 (1990).

    Google Scholar 

  39. V. V. Dovlatyan, L. L. Gyul'budagyan, and E. N. Ambartsumyan, Arm. Khim. Zh., 36, 404 (1983).

    Google Scholar 

  40. G. S. Amazaspyan, E. N. Ambartsumyan, and V. V. Dovlatyan, Arm. Khim. Zh., 43, 710 (1990).

    Google Scholar 

  41. V. V. Dovlatyan, L. L. Gyul'budagyan, and E. N. Ambartsumyan, Arm. Khim. Zh., 35, 322 (1982).

    Google Scholar 

  42. V. V. Dovlatyan, E. N. Ambartsumyan, and G. S. Amazaspyan, Arm. Khim. Zh., 43, 267 (1990).

    Google Scholar 

  43. V. V. Dovlatyan, L. L. Gyul'budagyan, and E. N. Ambartsumyan, Arm. Khim. Zh., 40, 714 (1987).

    Google Scholar 

  44. E. N. Ambartsumyan, G. S. Amazaspyan, and V. V. Dovlatyan, Arm. Khim. Zh., 43, 460 (1990).

    Google Scholar 

  45. J. C. Petitpierre and H. Ackerman, Ger. Patent 2263853; Chem. Abstr., 79, 92293 (1973).

    Google Scholar 

  46. G. Rembarz, E. Fischer, S. Iakubowsky, and R. Evers, Wiss. Z. Wilchelm-Pieck-Univ. Rostok. Naturwiss. R, 31, 11 (1982).

    Google Scholar 

  47. R. Freiberg and F. Bulka, J. Prakt. Chem., 329, 259 (1987).

    Google Scholar 

  48. H. J. Diehr, Ch. Fest, R. Kirsten, J. Kluth, and K. Mueller, Ger. Patent 3517821; Chem. Abstr., 105, 42850 (1986).

    Google Scholar 

  49. V. V. Dovlatyan, L. A. Khachatryan, and E. N. Ambartsumyan, Arm. Khim. Zh., 32, 799 (1982).

    Google Scholar 

  50. S. A. Khasanov, Ch. Sh. Kadyrov, and M. Akbarova, Khim. Prirod. Soedin., 704 (1979).

  51. R. P. Bokaldere, A. Ya. Liepin', I. B. Mazheika, I. S. Yankovska, and E. E. Liepin'sh, Khim. Geterotsikl. Soedin., 419 (1973).

  52. B. Vercek, B. Ogorevc, B. Stanovnik, and M. Tisler, Monatsh. Chem., 114, 789 (1983).

    Google Scholar 

  53. C. W. Thornber, J. M. Farrell, and D. S. Clarke, Synthesis, 222 (1983).

  54. L. M. Werbel, A. Curry, E. F. Elslager, and C. Hess, J. Heterocycl. Chem., 10, 363 (1973).

    Google Scholar 

  55. V. A. Dorokhov and M. F. Gordeev, Izv. Akad. Nauk. Ser. Khim., 1211 (1989).

  56. V. A. Dorokhov, M. F. Gordeev, Z. K. Dem'yanets, M. N. Bochkareva, and V. S. Bogdanov, Izv. Akad. Nauk. Ser. Khim., 1806 (1989).

  57. V. A. Dorokhov, M. F. Gordeev, Z. K. Dem'yanets, M. N. Bochkareva, L. G. Vorontsova, and M. G. Kurella, Izv. Akad. Nauk. Ser. Khim., 407 (1990).

  58. Yu. S. Andreichikov and D. D. Nekrasov, Zh. Org. Khim., 24, 2237 (1988).

    Google Scholar 

  59. L. L. Gyul'budagyan, E. N, Ambartsumyan, and V. V. Dovlatyan, Arm. Khim. Zh., 42, 518 (1989).

    Google Scholar 

  60. G. S. Amazaspyan, E. N. Ambartsumyan, and V. V. Dovlatyan, Arm. Khim. Zh., 45, 84 (1992).

    Google Scholar 

  61. V. V. Dovlatyan, E. N. Ambartsumyan, and G. S. Amazaspyan, Khim. Geterotsikl. Soedin., 84 (1996).

  62. V. V. Dovlatyan, L. L. Gyul'budagyan, and E. N. Ambartsumyan, Arm. Khim. Zh., 36, 399 (1983).

    Google Scholar 

  63. V. V. Dovlatyan, K. A. Eliazyan, V. A. Pivazyan, and A. M. Akopyan, Khim. Geterotsikl. Soedin., 818 (1993).

  64. V. A. Dorokhov and M. F. Gordeev, Izv. Akad. Nauk. Ser. Khim., 458 (1987).

  65. V. A. Dorokhov, M. F. Gordeev, and Z. K. Dem'yanets, Khim. Geterotsikl. Soedin., 1424 (1987).

  66. T. Sasaki and E. Ito, J. Heterocycl. Chem., 18, 1353 (1981).

    Google Scholar 

  67. T. Itaya and K. Ogawa, Tetrahedron Lett., 2907 (1978).

  68. T. Itaya and K. Ogawa, Tetrahedron Lett., 38, 1767 (1982).

    Google Scholar 

  69. D. W. Wilei, O. W. Webster, and E. P. Banchard, J. Org. Chem., 43, 3427 (1978).

    Google Scholar 

  70. N. I. Kos and H. C. Plas, J. Org. Chem., 45, 2942 (1980).

    Google Scholar 

  71. P. Victory and M. Garriga, Heterocycles, 23, 1947 (1985).

    Google Scholar 

  72. H. Kristianson, J. Chem. Soc., Chem. Commun., 350 (1974).

  73. V. V. Dovlatyan, Khim. Geterotsikl. Soedin., 17 (1998).

  74. D. D. Nekrasov, Yu. S. Andreichikov, S. N. Shurov, and L. N. Karpova, International Conference. Scientific Principles of the Creation of Chemotherapeutic Agents [in Russian], Ekaterinburg (1993), p. 6.

  75. S. A. Bakunov, A. V Rukovisnikov, and A. V. Tjachev, Synthesis, 8, 1148 (2000).

    Google Scholar 

  76. S. V. Pan'kov, N. A. Belyaeva, V. V. Vishnyakov, and P. P. Purygin, Zh. Org. Khim., 37, 451 (2001).

    Google Scholar 

  77. N. Ocal and J. Erden, Tetrahedron Lett., 42, 4765 (2001).

    Google Scholar 

  78. D. D. Nekrasov and S. N. Shurov, in: Prospects for the Development of Natural Sciences in the High School [in Russian], Perm (2002), Vol. 1, pp. 56-60.

    Google Scholar 

  79. N. A. Klenova and Z. P. Belousova, Khim.-Farm. Zh., 36, No. 8, 45 (2002).

    Google Scholar 

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Nekrasov, D.D. Hetarylcyanamides. (Review). Chemistry of Heterocyclic Compounds 40, 1107–1123 (2004). https://doi.org/10.1023/B:COHC.0000048282.79781.88

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  • DOI: https://doi.org/10.1023/B:COHC.0000048282.79781.88

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