Synthesis of Pyrimido[4,5-e]tetrazolo[5,1-b][1,3,4]thiadiazepine as a Novel Fused Heterocyclic System

References

• S. Sahi and S. Paul, “Synthesis and Biological Evaluation of Quinolines, Thiazolo[3,2-a]Pyrimidines, Thiadiazolo[3,2-a]Pyrimidines and Triazolo[3,4-b][1,3,4]thiadiazepines as antimicrobial agents,” Medicinal Chemistry Research 25, (2016): 951–69. doi: 10.1007/s00044-016-1540-z.
   Web of Science ®Google Scholar
• M. Kidwai, P. Sapra, P. Misra, R. K. Saxena, and M. Singh, “Microwave Assisted Solid Support Synthesis of Novel 1,2,4-Triazolo[3,4-b]-1,3,4-Thiadiazepines as Potent Antimicrobial Agents,” Bioorganic & Medicinal Chemistry 9, (2001): 217–20. doi: 10.1016/S0968-0896(00)00245-5.
   PubMed Web of Science ®Google Scholar
• V. M. Reddy and K. R. Reddy, “Synthesis and Antibacterial Activity of Some Novel 6-(1H-Benz[d]Imidazol-2-yl)-8-(5-Nitro-2-Furyl)-3-(4-Pyridyl)-7,8-Dihydro[1,2,4]Triazolo[3,4-b][1,3,4]Thiadiazepines,” Chemical and Pharmaceutical Bulletin 58, (2010):1081–84. doi: 10.1248/cpb.58.1081.
   PubMed Web of Science ®Google Scholar
• A. Brukstus, D. Melamedaite, and S. Tumkevicius, “A Facile Synthesis of Benzo[4,5]Imidazo[2,1-b]-Pyrimido[5,4-f][1,3,4]Thiadiazepines,” Synthetic Communications 30, (2000): 3719–30. doi: 10.1080/00397910008086999.
   Web of Science ®Google Scholar
• I. H. El-Azab, “Synthesis of Some New Benzo[b][1, 4]diazepine Based Heterocycles,” Journal of Heterocyclic Chemistry 50, (2013):E178–E188. doi: 10.1002/jhet.1123.
   Web of Science ®Google Scholar
• A. Dandia, R. Singh, and S. Khaturia, “Microwave Enhanced Solid Support Synthesis of Fluorine Containing Benzopyrano-triazolo-thiadiazepines as Potent Anti-Fungal Agents,” Bioorganic & Medicinal Chemistry 14, (2006): 1303–08. doi: 10.1016/j.bmc.2005.09.057.
   PubMed Web of Science ®Google Scholar
• H. Kantarjian, N. P. Shah, A. Hochhaus, J. Cortes, S. Shah, M. Ayala, B. Moiraghi, Z. Shen, J. Mayer, R. Pasquini, H. Nakamae, F. Huguet, C. Boqué, C. Chuah, E. Bleickardt, M. B. Bradley-Garelik, C. Zhu, T. Szatrowski, D. Shapiro, and M. Baccarani, “Dasatinib Versus Imatinib in Newly Diagnosed Chronic-Phase Chronic Myeloid Leukemia,” The New England Journal of Medicine 362, (2010): 2260–70. doi: 10.1056/NEJMoa1002315.
   PubMed Web of Science ®Google Scholar
• I. Susvilo, A. Brukstus, and S. Tumkevicius, “Transformation of Methyl N-Methyl-N-(6-Substituted-5-Nitro-4-Pyrimidinyl)Aminoacetates into 4-Methylamino-5-Nitrosopyrimidines and 9-Methylpurin-8-Ones,” Tetrahedron Letters 46, (2005): 1841–44. doi: 10.1016/j.tetlet.2005.01.119.
   Web of Science ®Google Scholar
• S. B. Bavage, Synthesis of 1, 2, 4-Triazole, 1-Amino Sulphonamyl Derivatives of Thiazolidin 4-Ones and Development of Hplc Method for Assay of Drugs in Formulations (Belagavi, Karnataka: KLE University, 2011).
   Google Scholar
• A. Kakehi, S. Ito, F. Ishida, and Y. Tominaga, “Preparation of New Nitrogen-Bridged Heterocycles. 43.1 Synthesis and Reaction of 5a H-Pyrido[1,2-d][1,3,4]Thiadiazepine Derivatives,” The Journal of Organic Chemistry 62, (1997): 7788–93. doi: 10.1021/jo971066o.
   Web of Science ®Google Scholar
• G. Albano and L. A. Aronica, “Potentiality and Synthesis of O- and N-Heterocycles: Pd-Catalyzed Cyclocarbonylative Sonogashira Coupling as a Valuable Route to Phthalans, Isochromans, and Isoindolines,” European Journal of Organic Chemistry 2017, (2017): 7204–21. doi: 10.1002/ejoc.201701041.
   Web of Science ®Google Scholar
• P. Molina, M. J. Lidón, and A. Tárraga, “Synthetic Applications of C,C-Bis(Iminophosphoranes): Preparation of [5+5] Rigid Bicyclic Guanidines and 1,3,6-Benzothiadiazepino[3,2-a]Benzimidazole Derivatives,” Tetrahedron 50, (1994): 10029–36. doi: 10.1016/S0040-4020(01)89618-6.
   Web of Science ®Google Scholar
• D. Hesek, and A. Rybar, “[f]-Fused Purine-2,6-Diones: Synthesis of new [1,3,5]- and [1,3,6]-Thiadiazepino-[3,2-f]-Purine Ring Systems,” Monatshefte Für Chemie/Chemical Monthly 125, (1994): 1273–78. doi: 10.1007/BF00813814.
   Web of Science ®Google Scholar
• N. N. Volkova, E. V, Tarasov, L. Van Meervelt, S. Toppet, W. Dehaen, and V. A. Bakulev., “Reaction of 5-Halo-1,2,3-Thiadiazoles With Aliphatic Diamines. Synthesis and Intramolecular Cyclization of Bis(1,2,3-Triazolyl-1,2,3-Thiadiazolyl)Sulfides,” Organic & Biomolecular Chemistry 1, (2003): 4030–38. doi: 10.1039/b307693h.
   PubMed Web of Science ®Google Scholar
• N. N. Volkova, E. V. Tarasov, L. Van Meervelt, S. Toppet, W. Dehaen, and V. A. Bakulev, “Reaction of 5-Halo-1,2,3-Thiadiazoles With Arylenediamines as a New Approach to Tricyclic 1,3,6-Thiadiazepines,” Journal of the Chemical Society, Perkin Transactions 1 (2002): 1574–80. doi: 10.1039/B203072A.
   Google Scholar
• N. Noorolahian and A. Shiri, “Synthesis of Some Derivatives of Pyrimido[5,4-e]Tetrazolo[5,1-c][1,2,4]Triazine; a Novel Heterocyclic System,” Journal of Chemical Research 39, (2015): 609–11. doi: 10.3184/174751915X14428472915706.
   Google Scholar
• M. Bakavoli, M. Rahimizadeh, A. Shiri, H. Eshghi, P. Pordeli, M. Pordel, and M. Nikpour., “Synthesis and Antibacterial Evaluations of New Pyridazino [4,3-e][1,3,4]Oxadiazines,” Journal of Heterocyclic Chemistry 48, (2011): 149–52. doi:10.1002/jhet.398.
   Web of Science ®Google Scholar
• M. Rahimizadeh, A. Shiri, M. Ranaei, and M. Bakavoli., “Synthesis and Antibacterial Evaluation of New Heterocyclic System: [1,2,4]Triazolo[3′,4′: 6,1]Pyridazino[4,3-e][1,3,4]Thiadiazine,” Heterocyclic Communications 18, (2012) 39–42. doi: 10.1515/hc-2011-0051.
   Web of Science ®Google Scholar
• M. Akbarzadeh, M. Bakavoli, H. Eshghi, and A. Shiri., “Synthesis of Oxazolo[5,4-d][1,2,4]Triazolo[4,3-a]Pyrimidines as a New Class of Heterocyclic Compounds,” Journal of Heterocyclic Chemistry 53, (2016): 832–39. doi: 10.1002/jhet.2346.
   Web of Science ®Google Scholar
• S. S. Mozafari, A. Shiri, M. Bakavoli, M. Akbarzadeh, and K. Saadat, “Synthesis and Density Functional Theory Study of [1,2,3]Triazolo[4,5-d][1,2,4]Triazolo [4,3-a]Pyrimidine Derivatives: A Novel Heterocyclic System,” Journal of Chemical Research 40, (2016): 633–36. doi: 10.3184/174751916X14743011878429.
   Google Scholar
• Y. Etemadi, A. Shiri, H. Eshghi, M. Akbarzadeh, K. Saadat, S. Mozafari, H. Beyzaei, and M. Moghaddam-Manesh, “Synthesis, Characterisation, and in Vitro Antibacterial Evaluation of a New Class of 2-Substituted-4-Methyl-7,8-Dihydro-5H-Pyrimido[4,5-d]Thiazolo[3,2-a]Pyrimidines,” Journal of Chemical Research 40, (2016): 600–03. doi:10.3184/174751916X14737838285904.
   Google Scholar
• Z. Ebrahimpour, M. Bakavoli, A. Shiri, M. S. Seyedi, T. Asghari, and J. T. Mague., “Synthesis, X-Ray and Fluorescence Characteristics of Pyrimido[5,4-e]Thiazolo [3,2-a] Pyrimidine as a Novel Heterocyclic System,” Journal of Fluorescence 27, (2017): 1183–90. doi: 10.1007/s10895-017-2055-9.
   PubMed Web of Science ®Google Scholar
• M. Akbarzadeh, M. Bakavoli, H. Eshghi, A. Shiri, and J. Tajabadi., “Synthesis of Dihydrobenzo[b]pyrimido[4,5-e][1,4]Thiazepines; Derivatives of a Novel Ring System,” Journal of Chemical Research 39, (2015): 531–34. doi:10.3184/174751915X14401726334645.
   Web of Science ®Google Scholar
• H. Eshghi, M. Rahimizadeha, S. Saberia, Kh. Abnousb, and M. Bakavolia., “Pyrimido[5,4-e]Tetrazolo[5,1-b][1,3,4]Thiadiazines as a New Heterocyclic System,” Journal of Chemical Research 37, (2013): 553–55. doi:10.3184/174751913X13738978141695.
   Google Scholar
• N. Firoozi, M. Bakavoli, H. Eshghi, N. Ramazanian, and M. Akbarzadeh, “Synthesis of Pyrimido[4′,5′: 5,6][1,4]Dithiepino[2,3-b]Quinoxalines: Derivatives of a Novel Seven Membered Ring System,” Phosphorus, Sulfur, and Silicon and the Related Elements 192, (2017): 442–45. doi: 10.1080/10426507.2016.1248290.
   Web of Science ®Google Scholar