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Three-Component One-Pot Synthesis of 4,6-Diarylpyrimidin-2(1H)-ones Catalyzed by 1-Methyl-3-[2-(sulfooxy)ethyl]-1H-imidazol-3-ium Chloride
Corresponding Author(s) : Hui Wu
Asian Journal of Chemistry,
Vol. 25 No. 11 (2013): Vol 25 Issue 11
Abstract
An efficient, one-pot, three-component cyclocondensation reaction of aromatic aldehydes, aromatic ketone and urea catalyzed by 1-methyl-3-[2-(sulfooxy)ethyl]-1H-imidazol-3-ium chloride is developed to give 4,6-diarylpyrimidin-2(1H)-ones.
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- P. Salehi, M. Dabiri, A.R. Khosropour and P. Roozbehniya, J. Iran. Chem. Soc., 3, 98 (2006).
- D. Russowsky, E.V. Benvenutti, G.S. Roxo and F. Grasel, Lett. Org. Chem., 4, 39 (2007).
- N. Rameshwar, T. Parthasarathy and A.R. Reddy, Indian J. Chem., 47B, 1871 (2008).
- T.B. Shah, A. Gupte, M.R. Patel, V.S. Chauhari, H. Patel and V.C. Patel, Indian J. Chem., 48B, 88 (2009).
- C.O. Kappe, Eur. J. Med. Chem., 35, 1043 (2000).
- B. Gangadasu, P. Narender, B.C. Raju and V.J. Rao, Indian J. Chem., 45B, 1259 (2006).
- K.S. Atwal, B.N. Swanson, S.E. Umger and D.M. Floyd, S. Moreland, A. Hedberg and B.C. O'Reilly, J. Med. Chem., 34, 806 (1991).
- S. Bartolini, A. Mai, M. Artico, N. Paesano, D. Rotili, C. Spadafora and G. Sbardella, J. Med. Chem., 48, 6776 (2005).
- G. Biginelli, Chim. Ital., 23, 360 (1893).
- L.Z. Wang, X.Q. Bian, H. Liu, Q. Sun and C.D. Wang, J. Chem. Res., 34, 694 (2010).
- Z. Pourghobadi and F. Derikvand, Chin. Chem. Lett., 21, 269 (2010).
- M.M. Heravi, F. Derikvand and L. Ranjbar, Synth. Commun., 40, 1256 (2010).
- M.M. Heravi, L. Ranjbar, F. Derikvand, B. Alimadadi and H.A. Oskooie, Mol. Divers, 12, 191 (2008).
- A.R. Khosropour, I. Mohammadpoor-Baltork and H. Ghorbankhani, Catal. Commun., 7, 713 (2006).
- A.R. Khosropour, B.I. Mohammadpoor and J. Mahbubeh, Heterocycles, 68, 1551 (2006).
- H. Wu, Y. Wan, X.M. Chen, C.F. Chen, L.-L. Lu, H.-Q. Xin, H.-H. Xu, L.-L. Pang, R. Ma and C.-H. Yue, J. Heterocycl. Chem., 46, 702 (2009)
References
P. Salehi, M. Dabiri, A.R. Khosropour and P. Roozbehniya, J. Iran. Chem. Soc., 3, 98 (2006).
D. Russowsky, E.V. Benvenutti, G.S. Roxo and F. Grasel, Lett. Org. Chem., 4, 39 (2007).
N. Rameshwar, T. Parthasarathy and A.R. Reddy, Indian J. Chem., 47B, 1871 (2008).
T.B. Shah, A. Gupte, M.R. Patel, V.S. Chauhari, H. Patel and V.C. Patel, Indian J. Chem., 48B, 88 (2009).
C.O. Kappe, Eur. J. Med. Chem., 35, 1043 (2000).
B. Gangadasu, P. Narender, B.C. Raju and V.J. Rao, Indian J. Chem., 45B, 1259 (2006).
K.S. Atwal, B.N. Swanson, S.E. Umger and D.M. Floyd, S. Moreland, A. Hedberg and B.C. O'Reilly, J. Med. Chem., 34, 806 (1991).
S. Bartolini, A. Mai, M. Artico, N. Paesano, D. Rotili, C. Spadafora and G. Sbardella, J. Med. Chem., 48, 6776 (2005).
G. Biginelli, Chim. Ital., 23, 360 (1893).
L.Z. Wang, X.Q. Bian, H. Liu, Q. Sun and C.D. Wang, J. Chem. Res., 34, 694 (2010).
Z. Pourghobadi and F. Derikvand, Chin. Chem. Lett., 21, 269 (2010).
M.M. Heravi, F. Derikvand and L. Ranjbar, Synth. Commun., 40, 1256 (2010).
M.M. Heravi, L. Ranjbar, F. Derikvand, B. Alimadadi and H.A. Oskooie, Mol. Divers, 12, 191 (2008).
A.R. Khosropour, I. Mohammadpoor-Baltork and H. Ghorbankhani, Catal. Commun., 7, 713 (2006).
A.R. Khosropour, B.I. Mohammadpoor and J. Mahbubeh, Heterocycles, 68, 1551 (2006).
H. Wu, Y. Wan, X.M. Chen, C.F. Chen, L.-L. Lu, H.-Q. Xin, H.-H. Xu, L.-L. Pang, R. Ma and C.-H. Yue, J. Heterocycl. Chem., 46, 702 (2009)