Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
Synthesis 2013; 45(14): 1950-1954
DOI: 10.1055/s-0033-1338454
DOI: 10.1055/s-0033-1338454
paper
Efficient Synthesis of 1,3,4-Oxadiazoles Conjugated to Thiophene or Furan Rings via an Ethenyl Linker
Further Information
Publication History
Received: 11 March 2013
Accepted after revision: 08 April 2013
Publication Date:
08 May 2013 (online)
Abstract
A novel and efficient synthesis of 5-substituted 2-[2-(2-furyl)ethenyl]-1,3,4-oxadiazoles and 2-[2-(2-thienyl)ethenyl]-1,3,4-oxadiazoles by cyclocondensation of the appropriate 3-(2-furyl)- and 3-(2-thienyl)acrylohydrazides with triethyl orthoesters in the presence of glacial acetic acid is reported. The formation of symmetrically substituted 2,5-bis[2-(2-furyl)ethenyl]-1,3,4-oxadiazole and 2,5-bis[2-(2-thienyl)ethenyl]-1,3,4-oxadiazole from the corresponding N,N′-diacylhydrazines under the influence of phosphorus oxychloride is also described.
-
References
- 1a Kraft A, Grimsdale AC, Holmes AB. Angew. Chem. Int. Ed. 1998; 37: 402
- 1b Segura JL. Acta Polym. 1998; 49: 319
- 1c Mitschke U, Bauerle P. J. Mater. Chem. 2000; 10: 1471
- 2a Schulz B, Bruma M, Brehmer L. Adv. Mater. (Weinheim, Ger.) 1997; 9: 601
- 2b Thelakkat M, Schmidt HW. Polym. Adv. Technol. 1998; 9: 429
- 3a Wang C, Jung GY, Batsanov AS, Bryce MR, Petty MC. J. Mater. Chem. 2002; 12: 173
- 3b Waskiewicz K, Gabański R, Żak J, Suwiński J. Electrochem. Solid-State Lett. 2005; 8: E24
- 3c Fuks-Janczarek I, Reshak AH, Kuźnik N, Kityk IV, Gabański R, Łapkowski M, Motyka R, Suwiński J. Spectrochim. Acta, Part A 2009; 72: 394
- 3d Łapkowski M, Motyka R, Suwiński J, Data P. Macromol. Chem. Phys. 2012; 231: 29
- 3e Data P, Łapkowski M, Motyka R, Suwiński J. Electrochim. Acta 2012; 59: 567
- 4a Schulz B, Orgzall I, Freydank A, Xii C. Adv. Colloid Interface Sci. 2005; 116: 143
- 4b Chen ZK, Meng H, Lai YH, Huang W. Macromolecules 1999; 32: 4351
- 4c Tamoto N, Adachi C, Nagai K. Chem. Mater. 1997; 9: 1077
- 4d Sinigersky V, Wegner G, Schopov I. Eur. Polym. J. 1993; 29: 617
- 5 Ainsworth C. J. Am. Chem. Soc. 1955; 77: 1148
- 6 Suwiński J, Szczepankiewicz W. Comprehensive Heterocyclic Chemistry III . Vol. 5. Katritzky AR, Ramsden CA, Scriven EF. V, Taylor RJ. K. Chap. 6 Elsevier Science Ltd; Oxford: 2008: 398
- 7a Amir M, Shikha K. Eur. J. Med. Chem. 2004; 39: 535
- 7b Almasirad A, Tabatabai SA, Faizi M, Kebriaeezadeh A. Bioorg. Med. Chem. Lett. 2004; 14: 6057
- 7c Rajapakse HA, Zhu H, Young MB, Mott BT. Tetrahedron Lett. 2006; 47: 4827
- 7d Zheng X, Li Z, Wang Y, Chen W, Huang Q, Liu C, Song G. J. Fluorine Chem. 2003; 123: 163
- 7e Zou XJ, Lai LH, Zhang ZX. J. Agric. Food Chem. 2002; 50: 3757
- 8 Dabiri M, Salehi P, Baghbanzadeh M, Bahramnejad M. Tetrahedron Lett. 2006; 47: 6983
- 9a Kudelko A, Zieliński W, Ejsmont K. Tetrahedron 2011; 67: 7838
- 9b Kudelko A. Tetrahedron 2012; 68: 3616
- 9c Kudelko A, Zieliński W. Tetrahedron Lett. 2012; 53: 76
- 10a Tully WR, Cardner CR, Gillespie RJ, Westwood R. J. Med. Chem. 1991; 34: 2060
- 10b Cao S, Qian X, Song G, Huang Q. J. Fluorine Chem. 2002; 117: 63
- 10c El Kain L, Le Menestrel I, Morgentin R. Tetrahedron Lett. 1998; 39: 6885
- 10d Tandon VK, Chhor RB. Synth. Commun. 2001; 31: 1727
- 10e Brain CT, Paul JM, Loong Y, Oakley PJ. Tetrahedron Lett. 1999; 40: 3275
- 11a Shaker RM, Mahmoud AF, Abdel-Latif FF. Phosphorus, Sulfur Silicon Relat. Elem. 2005; 180: 397
- 11b Zarghi A, Hajimahdi Z, Mohebbi S, Rashidi H, Mozaffari S, Sarraf S, Faizi M, Tabatabaee SA, Shafiee A. Chem. Pharm. Bull. 2008; 56: 509
- 11c Xie Y, Liu J, Yang P, Shi X, Li J. Tetrahedron 2011; 67: 5369
- 12a Buscemi S, Pace A, Pibiri I, Vivona N. J. Org. Chem. 2002; 67: 6253
- 12b Dupau P, Epple R, Thomas AA, Fokin VV, Sharpless KB. Adv. Synth. Catal. 2002; 344: 421
- 12c Huisgen R, Sauer J, Sturm HJ, Markgraf JH. Chem. Ber. 1960; 93: 2106
- 13 Karminski-Zamola G, Jakopcic K. Croat. Chem. Acta 1974; 46: 71
- 14 Singh S, Arthur JC. Carbohydr. Res. 1971; 17: 353
- 15 Yale HL, Losee K, Martins J, Holsing M, Perry FM, Bernstein J. J. Am. Chem. Soc. 1953; 75: 1933
- 16 Sugihara A, Ito M. Yakugaku Zasshi 1965; 85: 418 ; Chem. Abstr. 1965, 63, 5640
- 17 Karakhanov RA, Kelarev VI, Koshelev VN, Morozova GV, Dibi A. Chem. Heterocycl. Compd. (N.Y.) 1995; 31: 208