RSS-Feed abonnieren
DOI: 10.1055/s-0033-1338627
Thiazolothiadiazoles and Thiazolooxadiazoles: Synthesis and Biological Applications
Publikationsverlauf
Received: 04. Februar 2014
Accepted after revision: 27. März 2014
Publikationsdatum:
14. Mai 2014 (online)
Abstract
Recent advances in the diversity of synthetic routes available for the preparation of thiazolothiadiazoles and thiazolooxadiazoles are summarized and reviewed. The relative arrangements of the sulfur, oxygen, and nitrogen atoms and the various positions for fusion between the thiazole or oxazole and thiadiazole rings afford four different subclasses of thiazolothiadiazoles and thiazolooxadiazoles. Methods for synthesizing each of these subclasses are discussed separately. These compounds possess antimicrobial, antitubercular, anticancer, and anticonvulsant activities. The observed biological activities are due to the presence of the thiadiazole moiety, which displays diverse pharmacological activities. This short review can serve as a guide for synthetic and medicinal chemists wishing to develop novel thiazolothiadiazoles and thiazolooxadiazoles that can be evaluated as potential drugs.
1 Introduction
2 General Methods of Preparation
2.1 Synthesis of [1,3]Thiazolo[4,3-b][1,3,4]thiadiazoles and [1,3]Thiazolo[4,3-b][1,3,4]oxadiazoles
2.2 Synthesis of [1,3]Thiazolo[2,3-b][1,3,4]thiadiazoles
2.3 Synthesis of [1,3]Thiazolo[3,2-b][1,2,4]thiadiazoles
2.4 Synthesis of [1,3]Thiazolo[2,3-c][1,2,4]thiadiazoles
3 Biological Applications
4 Conclusion
-
References
- 1 Manoj Kumar P, Ravi TK, Chawla R, Bhuvana S, Sonia G. Indian J. Pharm. Sci. 2010; 72: 357
- 2 Khan RH, Rastogi RC. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 1988; 27: 501
- 3 Saundane AR, Manjunatha Y, Walmik P. Heterocycl. Commun. 2009; 15: 303
- 4 Yadav LD. S, Vaish A, Sharma S. J. Agric. Food Chem. 1994; 42: 811
- 5 Hagiwara K, Saitoh K, Iihama T, Kawana T, Hosaka H. J. Pestic. Sci. 1993; 18: 309
- 6 Abdel-Wahab BF, Mohamed HM. Phosphorus, Sulfur Silicon Relat. Elem. 2013; 188: 1680
- 7 Abdel-Wahab BF, Mohamed HM. Phosphorus, Sulfur Silicon Relat. Elem. 2014; 189: 157
- 8 Karigar AA, Himaja M. Int. J. Res. Ayurveda Pharm. 2011; 2: 170
- 9 Shukurov SS, Kukaniev MA, Alibaeva AM. Izv. Akad. Nauk, Ser. Khim. 1996; 763 ; Chem. Abstr. 1996, 125, 275763
- 10 Shukurov SS, Kukaniev MA, Alibaeva AM, Bobogaribov BM. Chem. Heterocycl. Compd. (Engl. Transl.) 1996; 32: 243
- 11 Bayoumy BE. Acta Pol. Pharm. 1991; 48: 13 ; Chem. Abstr. 1993, 118, 101880
- 12 Shukurov SS, Kukaniev MA, Alibaeva AM, Bobogaribov BM. Khim. Geterotsikl. Soedin. 1996; 271 ; Chem. Abstr. 1996, 125, 167883
- 13 Khan RH, Mathur RK, Ghosh AC. J. Chem. Res., Synop. 1996; 8: 388
- 14 Singh H, Yadav LS, Shukla SN, Dwivedi R. J. Agric. Food Chem. 1992; 40: 1409
- 15 Malipeddi H, Karigar AA, Malipeddi VR, Sikarwar MS. Trop. J. Pharm. Res. 2012; 11: 611 ; Chem. Abstr. 2012, 158, 243773
- 16 Himaja M, Karigar A, Ramana MV, Munirajasekhar D, Sikarwar MS. Lett. Drug Des. Discovery 2012; 9: 611
- 17 Karigar AA, Himaja M, Mali SV, Jagadeesh PK, Sikarwar MS. Int. Res. J. Pharm. 2011; 2: 153 ; Chem. Abstr. 2011, 155, 67899
- 18 Ali TE, Abdel-Aziz SA, El-Shaaer HM, Hanafy FI, El-Fauomy AZ. Phosphorus, Sulfur Silicon Relat. Elem. 2008; 183: 2139
- 19 Bayoumy BE, Skulski L. Bull. Pol. Acad. Sci. Chem. 1991; 39: 449 ; Chem. Abstr. 1992, 117, 233933
- 20 Singh H, Yadav LD. S, Chaudhary JP. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 1983; 60: 768 ; Chem. Abstr. 1984, 100, 139017
- 21 Yarovenko VN, Nikitina AS, Zavarzin IV, Krayushkin MM, Kovalenko LV. Russ. J. Org. Chem. (Engl. Transl.) 2007; 43: 1364
- 22 Tiwari N. J. Indian Chem. Soc. 1991; 68: 144
- 23 Singh K, Tiwari N. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 1993; 32: 1086
- 24 Mogilaiah K, Reddy PR, Rao RB. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 1999; 38: 1203
- 25 Mikitenko EK, Kachkovskii AD, Romanov NN. Khim. Geterotsikl. Soedin. 1982; 484
- 26 Mikitenko EK, Romanov NN. Khim. Geterotsikl. Soedin. 1981; 199 ; Chem. Abstr. 1981, 95, 7130
- 27 Sych ED, Mikitenko EK, Kornilov MY. Khim. Geterotsikl. Soedin. 1976; 778 ; Chem. Abstr. 1976, 85, 161854
- 28 Sych ED, Mikitenko EK. SU 478011, 1975 ; Chem. Abstr. 1975, 83, 193332.
- 29 Mikitenko EK, Romanov NN. Ukr. Khem. Zh. 1981; 47: 295 ; Chem. Abstr. 1981, 94, 210279
- 30 Yadav LD. S, Singh S. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2001; 40: 440
- 31 Siddiqui T, Alam MG. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2012; 51: 370
- 32 Siddiqui T, Alam MG. Chin. J. Chem. 2008; 26: 1339
- 33 Balaswamy G, Srinivas K, Pradeep P, Sarangapani M. Indian J. Heterocycl. Chem. 2012; 21: 365
- 34 Singh A. Indian J. Heterocycl. Chem. 2004; 43B: 901
- 35 Agrawal T, Tiwaa K, Nizamuddin MH. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 1994; 33: 603
- 36 Anand RS, Kalpana R, Manjunatha Y. Indian J. Heterocycl. Chem. 2012; 21: 193
- 37 Yadav LS, Rai VijaiK. Tetrahedron Lett. 2008; 49: 5553
- 38 Gupta M, Srivastava MK. J. Sci. Ind. Res. 1999; 58: 1017 ; Chem. Abstr. 2000, 132, 194326
- 39 Siddiqui IR, Dwivedi S, Shukla PK, Singh PK. J. Indian Chem. Soc. 2006; 83: 89
- 40 Kochhar MM, Salahi-Asbahi M, Williams BB. J. Pharm. Sci. 1973; 62: 336
- 41 Molina P, Arques A, Alias A. Tetrahedron 1992; 48: 1285
- 42 L’abbé G, Buelens J, Dehaen WA. J. Chem. Soc., Perkin Trans. 1 1993; 1825
- 43 Gardner JO, Beard CC. J. Pharm. Sci. 1979; 68: 182
- 44 Potts KT, Kane J. J. Org. Chem. 1975; 40: 2600
- 45 Baldwin D, Van den Broek P. J. Chem. Soc., Perkin Trans. 1 1975; 375
- 46 Potts KT, Kane JM. Synthesis 1986; 1027
- 47 Patel DS, Avalani JR, Raval DK. J. Braz. Chem. Soc. 2012; 23: 1951
- 48 Kushwaha N, Kushwaha KS, Rai AK. Int. J. ChemTech Res. 2012; 4: 517
- 49 Siddiqui N, Ahujaa P, Ahsan W, Pandeya SN, Alam MS. J. Chem. Pharm. Res. 2009; 1: 19
- 50 Asif K, Himaja M, Ramana MV, Sikrwar MS. Asian J. Chem. 2012; 24: 2739
- 51 Syed MA, Ramappa AK, Alegaon S. Asian J. Pharm Clin. Res. 2013; 6: 47
- 52 Hosny MA, Radwan HA, El-sawi EA. E-J. Chem. 2012; 9: 2
- 53 Mullick P, Khan SA, Verma S, Alam O. Bull. Korean Chem. Soc. 2011; 32: 1011