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Abbaspour-Gilandeh, Esmayeel, Azimi, Seyyedeh Cobra. (1394). The green synthesis of pyrano[3,2-c]quinoline-2,5-dione derivatives catalyzed by acidic ionic liquid under ultrasound irradiation. فصلنامه علمی زیست فناوری گیاهان زراعی, 3(Issue 3, pp. 180-282,Serial No. 8), 218-231.
Esmayeel Abbaspour-Gilandeh; Seyyedeh Cobra Azimi. "The green synthesis of pyrano[3,2-c]quinoline-2,5-dione derivatives catalyzed by acidic ionic liquid under ultrasound irradiation". فصلنامه علمی زیست فناوری گیاهان زراعی, 3, Issue 3, pp. 180-282,Serial No. 8, 1394, 218-231.
Abbaspour-Gilandeh, Esmayeel, Azimi, Seyyedeh Cobra. (1394). 'The green synthesis of pyrano[3,2-c]quinoline-2,5-dione derivatives catalyzed by acidic ionic liquid under ultrasound irradiation', فصلنامه علمی زیست فناوری گیاهان زراعی, 3(Issue 3, pp. 180-282,Serial No. 8), pp. 218-231.
Abbaspour-Gilandeh, Esmayeel, Azimi, Seyyedeh Cobra. The green synthesis of pyrano[3,2-c]quinoline-2,5-dione derivatives catalyzed by acidic ionic liquid under ultrasound irradiation. فصلنامه علمی زیست فناوری گیاهان زراعی, 1394; 3(Issue 3, pp. 180-282,Serial No. 8): 218-231.

The green synthesis of pyrano[3,2-c]quinoline-2,5-dione derivatives catalyzed by acidic ionic liquid under ultrasound irradiation

Iranian chemical communication
مقاله 32، دوره 3، Issue 3, pp. 180-282,Serial No. 8، مهر 2015، صفحه 218-231    اصل مقاله (276.18 K)
نوع مقاله: Original Research Article
نویسندگان
Esmayeel Abbaspour-Gilandeh* 1؛ Seyyedeh Cobra Azimi2
1islamic azad university of ardabil
2Islamic Azad University, rasht, Iran
چکیده
Abstract-A novel and efficient method has been developed for the synthesis of pyrano[3,2-c]quinoline-2,5-dione derivatives by the convenient ultrasound-mediated condensation of 4-hydroxyquinolin-2-one with Meldrum’s acid and aldehydes in the presence of a catalytic amount of [HMIm]HSO4 as a green, efficient and reusable acidic ionic liquid medium. The stability of the ionic liquid during the reaction was high and, used for several times to recycled form. Placing the reaction mixture under ultrasound condition causes that we have lower energy consumption and achieve to the desired product in the optimal time. The method is simple, starts from readily accessible commercial starting materials, and provides biologically interesting products in good yields and short reaction times.
کلیدواژه‌ها
Ultrasonic irradiation؛ Meldrum’s acid؛ pyrano[3,2-c]quinoline؛ ionic liquid
مراجع
[1] J.S. Torrecilla, J. Palomar, J.N. Garcí, F. Rodríguez, K. J. Chem. Eng. Data, 2009, 54, b1297.

[2] Roshan,N., Ghader, S., 2012. Developing models for correlating ionic liquids density: Part 1 – Density at 0.1 MPa., Fluid Phase Equilibria 331, p.33.

[3] Thermodynamics of room temperature ionic liquids: Thesis report for 2011, University of Aberdeen, Barcelo, P., May 2011.

 [4] R. Fortunato,C.A.M.A. Fonso, M.A.M. Reis, J.G. Crespo, J. Memb. Sci., 2004, 242, 197-209.

[5] M.M. Khodaei, A.R. Khosropour, S. Ghaderi, J. Iran. Chem. Soc., 2006, 3, 69-72.

[6] H.Y. Guo, Y.Yu, Chin. Chem. Lett., 2010, 21, 1435-1438.

[7] X. Mi, S. Luo, J.P. Cheng, J. Org. Chem., 2005, 70, 2338-2341.

[8] D.C. Chen, H.Q. Ye, H. Wu, Chin. Chem. Lett., 2007, 18, 27-29.

[9] A. Davoodnia, S. Allameh, A.R. Fakhari, Chin. Chem. Lett., 2010, 21, 550-553.

[10] A. Clark, Pharm Res., 1996, 13, 1133-1141.

[11] M. Anniyappan, D. Muralidhran, P.T. Perumal, Tetrahedron Lett., 2003, 44, 3653-3657.

[12] N. Ravindranath, C. Ramesh, M.R. Reddy, B. Das, Chem. Lett., 2003, 32, 222-223.

[13] I.C. Badhwar, K. Venkataraman, J. Chem. Soc., 1932, 2420-2423.

[14] T.S. Chen, S. J. Wu, I. L. Tsai, T. S., Wu, J.M. Pezzuto, M.C. Lu, H. Chai, N. Suh, C.M. Teng, J. Nat. Prod., 1994, 57, 1206-1211.

[15] T. Davion, B. Joseph, Y. Merour, Syn. Let., 1998, 1051-1052.

[16] Y. Fujita, H. Oguri, H. Oikawa. J. Antibiot., 2005, 58, 425-427.

[17] E.A. Mohamed, Chem. Pap., 1994, 48, 261-267.

[18] F. Hanawa, N. Fokialakis, A. L. Skaltsounis, Planta Med., 2004, 70, 531-535.

[19] M. Rufchahi M, A.G. Gilani, Dyes. Pigm., 2012, 95, 632-636.

[20] M.R. Shaaban, T.S. Saleh, F.H. Osman, A.M. Farag, J. Heterocycl. Chem., 2007, 44, 177-181.

[21] N.M. Abd El-Rahman, A.A. El-kateb, M.F. Mady, Synth. Commun., 2007, 37, 3961-3970.

[22] A.A. El-Kateb, N.M. Abd El-Rahman, Phos. Sulf. Silicon., 2006, 181, 249-259.

[23] J.Y. Winum, M. Kamal, A. Leydet, Tetrahedron Lett., 1996, 37, 1781-1785.

[24] J.T. Li, W.Z. Yang, S.X. Wang, S.H. Li, T.S. Li, Ultrason. Sonochem., 2002, 9, 237-239.

[25] S.X. Wang, J.T. Li, W.Z. Yang, T.S. Li, Ultrason. Sonochem., 2002, 9, 159-161.

[26] J.T. Li, T.S. Li, L.J. Li, X. Cheng, Ultrason. Sonochem., 1999, 6, 199-201.

[27] J.T. Li, L.J. Li, T.S. Li, H.Z. Li, I.K. Li, Ultrason. Sonochem., 1996, 3, 141-148.

[28] S.J. Ji, Z.L. Shen, D.G. Gu, X.Y. Huang, Ultrason. Sonochem., 2005, 12, 161-163.

[29] J.T. Li, M.X. Sun, Y. Yin, Ultrason. Sonochem., 2010, 17, 359-362.

[30] C.L. Ni, X.H. Song, H. Yan, X.Q. Song, R.G. Zhong, Ultrason. Sonochem., 2010, 17, 367-369.

[31] M. A. Margulis, Ultrasonics, 1992, 30, 152-155.

[32] R. M. Martin-Aranda, E. Ortega-Cantero, M. L. Rojas-Cervantes, M. A. Vicente-Rodrigues, M. A. Ban-Ares-Mun-Oz, Catal. Lett., 2002, 84, 201-204.

[33] V. Calvine-Casilda, A. J. Lopez. Peinado, R. M. Martin-Aranda, S. Ferrera-Escudero, C. J. Duran-Valle. Carbon, 2004, 42, 1363-1366.

[34] V. Tiwari, A. Parvez, J. Meshram, Ultrason. Sonochem., 2011, 18, 911-916.

[35] K. Rad-Moghadam, S.C. Azimi, E. Abbaspour-Gilandeh, Tetrahedron Lett., 2013, 54, 4633-4636.

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