SYNTHESIS AND CHEMICAL CONVERSIONS OF 2-BROMO-6-PHENYLIMIDAZO[2,1-<i>b</i>][1,3,4]THIADIAZOLE

Authors

  • М. А. Куканиев V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Tajikistan Republic, Dushanbe 734063
  • Р. Рахмонов V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Tajikistan Republic, Dushanbe 734063
  • C. Сафаров V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Tajikistan Republic, Dushanbe 734063
  • Ю. Ходжибаев V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Tajikistan Republic, Dushanbe 734063
  • Д. М. Осимов V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Tajikistan Republic, Dushanbe 734063

DOI:

https://doi.org/10.1007/7558

Keywords:

2-amino-5-bromo-1, 3, 4-thiadiazole, 2-bromo-6-phenylimidazo[2, 1-b]-1, 2, 5-dibromo-6-phenylimidazo[2, 2-morpholino-5-morpholinomethyl-6-phenylimidazo[2

Abstract

The interaction of 2-amino-5-bromo-1,3,4-thiadiazole with  ω-bromo-acetophenone leads to 2-bromo-6-phenylimidazo[2,1-b][1,3,4]thiadiazole. The bromine atom in position  2 of 2-bromo-6-phenyl-imidazo[2,1-b][1,3,4]thiadiazole is readily substituted by the action of secondary amines.

How to Cite
Kukaniev, M. A.; Rakhmonov, R.; Safarov, S.; Khodzhibaev, Yu.;  Osimov, D. M.  Chem. Heterocycl. Compd. 2007, 43, 499. [Khim. Geterotsikl. Soedin. 2007, 605.]

For this article in the English edition see DOI 10.1007/s10593-007-0073-2


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Published

2023-03-24

Issue

No. 4 (2007)

Section

Original Papers