Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

Trichloroisocyanuric Acid/Triphenylphosphine-Mediated Synthesis of Benzimidazoles, Benzoxazoles, and Benzothiazoles

Soodabeh Rezazadeh A , Batool Akhlaghinia A B and Nasrin Razavi A
+ Author Affiliations
- Author Affiliations

A Department of Chemistry, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad 9177948974, Iran.

B Corresponding author. Email: akhlaghinia@um.ac.ir

Australian Journal of Chemistry 68(1) 145-155 https://doi.org/10.1071/CH14037
Submitted: 26 January 2014  Accepted: 24 April 2014   Published: 25 June 2014

Abstract

A new and efficient method for preparation of benzimidazoles, benzoxazoles, and benzothiazoles from reactions of different carboxylic acids with o-phenylenediamine, o-aminophenol, and o-aminothiophenol in the presence of triphenylphosphine/trichloroisocyanuric acid system is presented. The desired products have been characterised on the basis of spectral (infrared, NMR, mass spectrometry) data, and the mechanism of their formation is proposed. The remarkable advantages are the inexpensive and readily available reagent, simple procedure, mild conditions, and good-to-excellent yields.


References

[1]     (a) A. R. Katritzky, J. M. Lagowski, in Comprehensive Heterocyclic Chemistry (Ed. K. T. Potts) 1984, Vol 5. Ch. 4.01, pp. 1–38 and Ch. 4.02, pp. 39–110 (Pergamon: Oxford).
         (b) K. T. Potts, in Comprehensive Heterocyclic Chemistry (Ed. K. T. Potts) 1984, Vol 5. Ch. 4.03, pp. 111–166 (Pergamon: Oxford).
      (c) C. Chen, Y.-J. Chen, Tetrahedron Lett. 2004, 45, 113.
         | Crossref | GoogleScholarGoogle Scholar |
      (d) G. Evindar, A. R. Batey, J. Org. Chem. 2006, 71, 1802.
         | Crossref | GoogleScholarGoogle Scholar |

[2]  (a) D. A. Horton, G. T. Bourne, M. L. Smythe, Chem. Rev. 2003, 103, 893.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXhtlGkt7k%3D&md5=b60b0197817d8d98c430df6bce0716e0CAS | 12630855PubMed |
      (b) A. A. Weekes, A. D. Westwell, Curr. Med. Chem. 2009, 16, 2430.
         | Crossref | GoogleScholarGoogle Scholar |

[3]  M. O. Chaney, P. V. Demarco, N. D. Jones, J. L. J. Occolowitz, J. Am. Chem. Soc. 1974, 96, 1932.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE2cXhtlOqtb8%3D&md5=d4d1f1540a09c73e0540de844d366384CAS | 4815763PubMed |

[4]  (a) A. R. Porcari, R. V. Devivar, L. S. Kucera, J. C. Drach, L. B. Townsend, J. Med. Chem. 1998, 41, 1252.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXhvFyhsro%3D&md5=b492921d47de56025fbcb721fe8764beCAS | 9548815PubMed |
      (b) X. Song, B. S. Vig, P. L. Lorenzi, J. C. Drach, L. B. Townsend, G. L. Amidon, J. Med. Chem. 2005, 48, 1274.
         | Crossref | GoogleScholarGoogle Scholar |

[5]  I. Yildiz-Oren, I. Yalcin, E. Aki-Sener, N. Ucarturk, Eur. J. Med. Chem. 2004, 39, 291.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXislWjt7Y%3D&md5=8ae737e7493cd17dc50341f6b84f6dd7CAS | 15051178PubMed |

[6]  (a) D. Kumar, M. R. Jacob, M. B. Reynolds, S. M. Kerwin, Bioorg. Med. Chem. 2002, 10, 3997.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38Xot1ensrY%3D&md5=43894420b0f259aa626b5acce36ff23cCAS | 12413851PubMed |
      (b) S. T. Huang, I. J. Hsei, C. Chen, Bioorg. Med. Chem. 2006, 14, 6106.
         | Crossref | GoogleScholarGoogle Scholar |

[7]  D. A. Evans, C. E. Sacks, W. A. Kleschick, T. R. Taber, J. Am. Chem. Soc. 1979, 101, 6789.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3cXlvVKlsA%3D%3D&md5=f244b8bcfc078c5f7290fbfc40bcc52dCAS |

[8]  M. Yamato, Yakugaku Zasshi 1992, 112, 81.
         | 1:CAS:528:DyaK38Xit1Onsbs%3D&md5=c9f2d74d0b89161593c3607c3d204118CAS | 1517979PubMed |

[9]  A. Benazzouz, T. Boraud, P. Dubèdat, A. Boireau, J.-M. Stutzmann, C. Gross, Eur. J. Pharmacol. 1995, 284, 299.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXot1yqsbw%3D&md5=4728e5ce493602def576e8936e318115CAS | 8666012PubMed |

[10]  M. Mader, A. de Dios, C. Shih, B. D. Anderson, Bioorg. Med. Chem. Lett. 2008, 18, 179.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXis1SrsQ%3D%3D&md5=7f5d7115ed0eb491f859865c55dd4c11CAS | 18039577PubMed |

[11]  (a) A. T. Mavrova, K. K. Anichina, D. I. Vuchev, J. A. Tsenov, P. S. Denkova, M. S. Kondeva, M. K. Micheva, Eur. J. Med. Chem. 2006, 41, 1412.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhtlagsbnJ&md5=7dd63943894af6cf360ed80c68b73be6CAS | 16996654PubMed |
      (b) Y. Kohara, K. Kubo, E. Imamiya, T. Wada, Y. Inada, T. Naka, J. Med. Chem. 1996, 39, 5228.
         | Crossref | GoogleScholarGoogle Scholar |
      (c) G. I. Elmer, J. O. Pieper, S. R. Goldberg, F. R. George, Psychopharmacology (Berl.) 1995, 117, 23.
         | Crossref | GoogleScholarGoogle Scholar |

[12]  J. Liu, Q. Liu, W. Xu, W. Wang, Chinese J. Chem. 2011, 29, 1739.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXht1Sit7nN&md5=2943e99eed4b50749039d61d8e86fd4cCAS |

[13]  X. Wen, J. El Bakali, R. Deprez-Poulain, B. Deprez, Tetrahedron Lett. 2012, 53, 2440.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XkvVGlu7Y%3D&md5=760e88e7e40b0013000c551522065f80CAS |

[14]  (a) Y. Riadi, R. Mamouni, R. Azzalou, M. El Haddad, S. Routier, G. Guillaumet, S. Lazar, Tetrahedron Lett. 2011, 52, 3492.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXntFGltLw%3D&md5=082ec8a81aa4e836e5914cf24dc10450CAS |
      (b) H. M. Bachhav, S. B. Bhagat, V. N. Telvekar, Tetrahedron Lett. 2011, 52, 5697.
         | Crossref | GoogleScholarGoogle Scholar |
      (c) A. J. Blacker, M. M. Farah, M. I. Hall, S. P. Marsden, O. Saidi, J. M. Williams, Org. Lett. 2009, 11, 2039.
         | Crossref | GoogleScholarGoogle Scholar |
      (d) M. A. Bigdeli, H. Dostmohammadi, G. H. Mahdavinia, F. Nemati, J. Heterocyclic Chem. 2008, 45, 1203.
         | Crossref | GoogleScholarGoogle Scholar |

[15]  D. F. Shi, T. D. Bradshaw, S. Wrigley, C. J. McCall, P. Lelieveld, I. Fichtner, M. F. Stevens, J. Med. Chem. 1996, 39, 3375.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28XksFahsbc%3D&md5=189efe9297711ded6d068df6fc2a5065CAS | 8765521PubMed |

[16]  V. K. Tandon, M. Kumar, Tetrahedron Lett. 2004, 45, 4185.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXjs1ertL4%3D&md5=9ef29b74550f805de4dce26ece3baf2bCAS |

[17]  (a) J. Charton, S. Girault-Mizzi, C. Sergheraert, Chem. Pharm. Bull. (Tokyo) 2005, 53, 492.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXlvVWiurw%3D&md5=8ce7288102d53122a9178d58e725e7eaCAS | 15863918PubMed |
      (b) J. A. Seijas, T. Vazquez, M. Pilar, R. Carballido, M. Raquel, C. J. Crecente, L. Romar-Lopez, Synlett 2007, 313.
         | Crossref | GoogleScholarGoogle Scholar |
      (c) M. B. Maradolla, S. K. Allam, A. Mandha, G. V. P. Chandramouli, ARKIVOC 2008, 15, 42.
         | Crossref | GoogleScholarGoogle Scholar |

[18]  (a) A. Kiani, B. Akhlaghinia, H. Rouhi-Sadabad, M. Bakavoli, J. Sulfur Chem. 2014, 35, 119.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXpt12htro%3D&md5=643a679f9385851d7f49b0ff9d735e37CAS |
      (b) B. Akhlaghinia, H. Rouhi-Sadabad, Can. J. Chem. 2013, 91, 181.
         | Crossref | GoogleScholarGoogle Scholar |

[19]  V. R. Shingalapur, M. K. Hosamani, Catal. Lett. 2010, 137, 63.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXksFKnt7Y%3D&md5=8d616f2e5d62ff1c86d9b16c0b2ed720CAS |

[20]  G. F. Chen, H. M. Jia, L. Y. Zhang, B. H. Chen, J. T. Li, Ultrason. Sonochem. 2013, 20, 627.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xhs1SqurrL&md5=f3943d9acf2e59464b033268410afd76CAS | 23122553PubMed |

[21]  K. Khosravi, S. Kazemi, Chinese Chem. Lett. 2012, 23, 61.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhs1Sru7rK&md5=fa48940443af1c13364380c788ccf894CAS |

[22]  X. Zhu, Y. Wei, X. Zhu, Heterocycl. Commun. 2012, 18, 211.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXls1ehsb4%3D&md5=8a75f7d7c9d0e35006ad54eb1d60509cCAS |

[23]  Kh. Bougrin, A. Loupy, M. Soufiaoui, Tetrahedron 1998, 54, 8055.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXktFOjsLY%3D&md5=27f20c470d81e6bdc10d5b207bfd1bf9CAS |

[24]  H. Eshghi, M. Rahimizadeh, A. Shiri, P. Sedaghat, Bull. Korean Chem. Soc. 2012, 33, 515.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XktFOmt74%3D&md5=5bb28eb3a9e2e356835146c752d5506fCAS |

[25]  L. Keurulainen, A. Siiskonen, P. Kiuru, J. Yli-Kauhaluoma, O. Salin, P. Vuorela, J. M. Kern, M. Maass, J. Alvesalo, J. Med. Chem. 2010, 53, 7664.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXht1KhsLfE&md5=4d6261282ce01b896dfc808975dce95aCAS | 20932010PubMed |

[26]  C. V. Ratnam, N. V. Subba Roa, Proc. Indian Acad. Sci. Sect. A 1956, 43, 173.

[27]  R. Cano, D. J. Ramon, M. Yus, J. Org. Chem. 2011, 76, 654.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhsF2ku73L&md5=92a0dc3db696ab1909af81a33f692fecCAS | 21175155PubMed |

[28]  S. S. Patil, V. D. Bobade, Synth. Commun. 2009, 40, 206.
         | Crossref | GoogleScholarGoogle Scholar |

[29]  L. I. Denisova, V. M. Kosareva, I. G. Solonenko, Pharm. Chem. J. 1976, 10, 1631.
         | Crossref | GoogleScholarGoogle Scholar |

[30]  H. Naeimi, N. Alishahi, J. Chin. Chem. Soc. 2012, 59, 1001.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xht1arurrP&md5=a98182c0826e656679e2cd31dd009cd1CAS |

[31]  A. A. Weekes, J. Frydrych, A. D. Westwell, Synth. Commun. 2013, 43, 2656.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXmtFSkt70%3D&md5=23064f65ade15097a4f18ae631c565f1CAS |

[32]  G. H. Mahdavinia, S. Rostamizadeh, A. M. Amani, H. Sepehrian, Heterocycl. Commun. 2012, 18, 33.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXls1ehs7c%3D&md5=84e0624e99e6b4ecda59f88e50ba4ea3CAS |

[33]  G. A. Molander, S. L. Trice, S. M. Kennedy, J. Org. Chem. 2012, 77, 8678.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhtlygtLjO&md5=cb8ee6047938b4f06b5df20b86e20cdcCAS | 22994557PubMed |

[34]  J. C. Lewis, A. M. Berman, R. G. Bergman, J. A. Ellman, J. Am. Chem. Soc. 2008, 130, 2493.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhsVWiurc%3D&md5=5eaee215ead616ab912094a40b01d4feCAS | 18251465PubMed |

[35]  L. Ackermann, A. Althammer, S. Fenner, Angew. Chem. Int. Ed. 2009, 48, 201.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXos1ChsA%3D%3D&md5=0e8ce047f952f8b160396cc8a3ca1d1cCAS |

[36]  R. Weidenhagen, Chem. Ber. 1936, 69, 2263.
         | Crossref | GoogleScholarGoogle Scholar |

[37]  V. N. Bochatay, P. J. Boissarie, S. Lang, J. A. Murphy, C. J. Suckling, J. Org. Chem. 2013, 78, 1471.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXntVehsQ%3D%3D&md5=ec02a05396bff3758ee091cfc5db6a22CAS | 23316812PubMed |

[38]  I. V. Védernikova, A. A. Konstantinchenko, Yu. I. Ryabukhin, Bull. Soc. Chim. Belg. 1991, 100, 175.
         | Crossref | GoogleScholarGoogle Scholar |

[39]  A. de Raadt, H. Griengl, M. Petsch, P. Plachota, N. Schoo, Tetrahedron Asymmetry 1996, 7, 473.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28XhsVCmur4%3D&md5=2b2bc5937304413c8a677fd6417fd40bCAS |

[40]  F. Besselièvre, S. Piguel, F. Mahuteau-Betzer, D. S. Grierson, Org. Lett. 2008, 10, 4029.
         | Crossref | GoogleScholarGoogle Scholar | 18720988PubMed |

[41]  L. Wang, X. Zhang, F. Li, Z. Zhang, Synth. Commun. 2004, 34, 2245.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXltV2qsro%3D&md5=2c6e7ebb76eb88a03f297ec62a05feb8CAS |

[42]  S. B. Lokhande, D. W. Rangnekar, Indian J. Chem. B 1986, 25, 485.

[43]  I. Dryanska, Dokl. Akad. Nauk 1970, 23, 1227.
         | 1:CAS:528:DyaE3MXjtFOjtA%3D%3D&md5=c9ff06df18cf7bef52194e98ee5dc36fCAS |

[44]  J. Gowda, A. M. A. Khadar, B. Kalluraya, N. S. Kumari, Indian J. Chem. B 2010, 49, 1130.

[45]  M. Skraup, Chem. Ber. 1922, 55, 1097.

[46]  H. Yu, M. Zhang, Y. Li, J. Org. Chem. 2013, 78, 8898.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXhtlSjurzP&md5=b5e1e229871cdfca66f830452313717bCAS | 23957712PubMed |

[47]  W. G. Bywater, W. R. Coleman, O. Kamm, H. Houston Merritt, J. Am. Chem. Soc. 1945, 67, 905.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaH2MXitVOhug%3D%3D&md5=4edbb3abd93ea1af65a8d3571105a9a2CAS |

[48]  X. Zhao, G. Wu, Y. Zhang, J. Wang, J. Am. Chem. Soc. 2011, 133, 3296.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXisVWms7k%3D&md5=7389f0474ceabbae3f9dd50dfbf13501CAS | 21341655PubMed |

[49]  R. N. Butler, K. J. Fitzgerald, J. Chem. Soc., Perkin Trans. 1 1989, 155.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1MXksFOltLw%3D&md5=0207aff03433e5de76d2dce718dd0cc6CAS |

[50]  K. Fierz-David, Helv. Chim. Acta 1939, 22, 89.

[51]  P. L. DuBrow, C. W. Hoerr, H. J. Harwood, J. Am. Chem. Soc. 1952, 74, 6241.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaG2cXntF2n&md5=dc6c129fc673f441c9f7423bb7d0ae5eCAS |

[52]  B. Decroix, P. Dubus, J. Morel, J. Morel, P. Pastour, Bull. Soc. Chim. Fr. 1976, 621.
         | 1:CAS:528:DyaE28XlslOgtb0%3D&md5=bbd99393af005fc000da98a12d1e3e71CAS |

[53]  V. I. Cohen, J. Heterocyclic Chem. 1979, 16, 13.
         | Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE1MXhvVKrt7Y%3D&md5=a2deba27505a163fbd2631f1b5544898CAS |

[54]  J. A. Mella-Raipán, C. F. Lagos, G. RecaBarren-Gajardo, C. Espinosa-Bustos, J. Romero-Parra, H. Pessoa-Mahana, P. Iturriaga-Vasquez, C. D. Pessoa-Mahana, Molecules 2013, 18, 3972.
         | Crossref | GoogleScholarGoogle Scholar | 23558540PubMed |

[55]  T. Maruyama, J. Koga, N. Kuroki, K. Konishi, Chem. Abstr. 1962, 58, 4669.

[56]  A. B. Naidu, G. Sekar, Synthesis 2010, 579.
         | 1:CAS:528:DC%2BC3cXjsFamt7c%3D&md5=5f2467b0fe5c48fe73b75cad1b7fb4bdCAS |