A green protocol for synthesis of pyran annulated hetrocyclic systems using Na2SO4 as an efficient catalyst

Iranian Journal of Catalysis

مقاله 10، دوره 5، شماره 2، شهریور 2015، صفحه 169-174   

نوع مقاله: Articles

نویسندگان

Malek Taher Maghsoodlou^* ؛ Amin Masoumnia؛ Mir Rasul Mousavi؛ Nourollah Hazeri؛ Jasem Aboonajmi؛ Sayyed Mostafa Habibi-Khorasani؛ Shiva Kiaee

Department of Chemistry, The University of Sistan and Baluchestan, P.O. Box 98135-674, Zahedan, Iran

چکیده

Na2SO4 as an inexpensive and effective catalyst has provided a green protocol for the synthesis of tetrahydrobenzo[b]pyran, pyrano[2,3-d]pyrimidinone and dihydropyrano[3,2c]chromene derivatives from the three-component domino reaction of aromatic aldehydes and malononitrile with 4-hydroxycoumarin/ dimedone/ barbituric acid in ethanol/water as a mixture of solvent that, this mixture entirely is green solvent. Products could simply be separated from the catalyst. Using neutral and mild conditions, short reaction time, environmentally benign procedure, high to excellent yields of the products and easy work-up without using column chromatography are the advantages of this method. By virtue of these advantages, sodium sulfate can be used as catalyst in the organic transformations.

کلیدواژه‌ها

Pyran annulated hetrocyclic systems؛ Na2SO4؛ Green protocol؛ Barbituric acid؛ 4-hydroxycoumarin

مراجع

[1] X. Zhang, A. Amer, X. Fan, J. Balzarini, J. Neyts, E. De Clercq, M. Prichard, E. Kern, P.F. Torrence, Bioorg. Chem. 35 (2007) 221-232.
[2] C. Luo, P. Xie, R. Marmorstein, J. Med. Chem. 51 (2008) 6121-6127.
[3] X. Fan, X. Zhang, L. Zhou, K.A. Keith, M.N. Prichard, E.R. Kern, P.F. Torrence, J. Med. Chem. 49 (2006) 4052-4054.
[4] S. Gao, C.H. Tsai, C. Tseng, C.F. Yao, Tetrahedron 64 (2008) 9143-9149.
[5] J. Marco-Contelles, R. Leon, C. de los Rıos, A.G. Garcıa, M.G. Lopez, M. Villarroya, Bioorg. Med. Chem. 14 (2006) 8176-8185.
[6] P.F. Torrence, X. Fan, X. Zhang, P.M. Loiseau, Bioorg. Med. Chem. Lett. 16 (2006) 5047-5051.
[7] I. Devi, P.J. Bhuyan, Tetrahedron Lett. 45 (2004) 8625-8627.
[8] S.B. Rajesh, V.M. Chandrakant, S.S. Kuldeep, B.M. Sandeep, S.C. Sunil, P.P. Rajendra, Synth. Commun. 37 (2007) 4353-4357.
[9] X.S. Wang, D.Q. Shi, S.J. Tu, C.S. Yao, Synth. Commun. 33 (2003) 119-126.
[10] S. Abdolmohammadi, S. Balalaie, Tetrhedron Lett. 48 (2007) 3299-3303.
[11] S. Gao, C.H. Tsai, C. Tseng, C.F. Yao, Tetrahedron 64 (2008) 9143-9149.
[12] M. Seifi, H. Sheibani, Catal. Lett. 126 (2008) 275-279.
[13] R. Hekmatshor, S. Majedi, K. Bakhtiari, Catal. Commun. 9 (2008) 307-310.
[14] Y.M. Ren, C. Cai, Catal. Commun. 9 (2008) 1017-1020.
[15] M.M. Heravi, B.A. Jani, F. Derikvand, F.F. Bamoharram, H.A. Oskooie, Catal. Commun. 10 (2008) 272-275.
[16] J.M. Khurana, S. Kumar, Tetrahedron Lett. 50 (2009) 4125-4127.
[17] W.O. Sun, P. Zhang, J. Fan, S.H. Chen, Z.H. Zhang, Synth. Commun. 40 (2010) 587-594.
[18] M.M. Khodaei, K. Bahrami, A. Farrokhi, Synth. Commun. 40 (2010) 1492-1499.
[19] D. Fang, H.B. Zhang, Z.L. Liu, J. Heterocycl. Chem. 47 (2010) 63-67.
[20] S.S. Katkar, M.K. Lande, B.R. Arbad, S.T. Gaikwad, Chin. J. Chem. 29 (2011) 199-202.
[21] J. Zheng, Y.Q. Li, Scholar Res. Lib. 3 (2011) 381-388.
[22] P.P. Salvi, A.M. Mandhare, A.S. Sartape, D.K. Pawar, S.H. Han, S.S. Kolekar, C. R. Chim.  14 (2011)  878-882.
[23] M.R. Mousavi, J. Aboonajmi, M.T. Maghsoodlou, N. Hazeri, S.M. Habibi-Khorassani, M. Safarzaei, Lett. Org. Chem. 10 (2013) 171-177.
[24] M.T. Maghsoodlou, K. Khandan-Barani, N. Hazeri, S.M. Habibi-Khorassani, A.C. Willis, Res. Chem. Intermed. 40 (2014)779-785.
[25] F. Farhadpour, N. Hazeri, S. Salahi, P. Dastoorani, R. Doostmohammadi, M. Lashkari, M. Ghashang, M.T. Maghsoodlou, Iran. J. Catal. 4 (2014) 247-251.
[26] N. Hazeri, S. Mohamadian-Souri, M.T. Maghsoodlou, M. Lashkari, M. Ghashang, Iran. J. Catal. Corrected Proof.
[27] H.J. Wang, J. Lu, Z.H. Zhang, Monatsh. Chem. 141 (2010) 1107-1112.
[28] H.R. Shaterian, M. Arman, F. Rigi, J. Mol. Liq. 158 (2011) 145-150.
[29] J.M. Khurana, B. Nand, P. Saluja, Tetrahedron 66 (2010) 5637-5641.
[30] S. Nemouchi, R. Boulcina, B. Carboni, A. Debache, C.R. Chim. 15 (2012) 394-397.
[31] A. Mobinikhaledi, M.A.B. Fard, Acta. Chim. Slov. 57 (2010) 931-935.
[32] S. Balalaie, M. Bararjanian, M. Sheikh‐Ahmadi, S. Hekmat, P. Salehi, Synth. Commun. 37 (2010) 1097-1108.
[33] L. Fotouhi, M.M. Heravi, A. Fatehi, K. Bakhtiari, Tetrahedron Lett. 48 (2007) 5379-5381.
[34] X.Z. Lian, Y. Huang, Y.Q. Li, W.J. Zheng, Monatsh. Chem. 139 (2008) 129-131.
[35] D.M. Pore, K.A. Undale, B.B. Dongare, U.V. Desai, Catal. Lett. 132 (2009) 104-108.
[36] J.Z. Qin, J.S. Jun, L. Jun, Y.J. Ming, Chin. J. Chem. 23 (2005) 1085-1089.
[37] Y. Gao, S. Tu, T. Li, X. Zhang, S. Zhu, F. Fang, D. Shi, Synth. Commun. 34 (2006) 1295-1299.