Three-component one-pot synthesis of 2,3-dihydroquinazolin-4(1H)-one derivatives in 2,2,2-trifluoroethanol

Comptes Rendus Chimie - Tập 15 - Trang 779-783 - 2012
Samad Khaksar1, Saeed Mohammadzadeh Talesh1
1Department of Chemistry, Ayatollah Amoli Branch, Islamic Azad University, Amol, Iran

Tài liệu tham khảo

Bégué, 2004, Synlett., 18 Westermaier, 2006, Org. Lett., 8, 4791, 10.1021/ol0618555 Ratnikov, 2008, Angew. Chem. Int. Ed., 47, 9739, 10.1002/anie.200803927 Westermaier, 2008, Chem. Eur. J., 14, 1638, 10.1002/chem.200701366 De, 2009, J. Org. Chem., 74, 6260, 10.1021/jo9012699 Nishiwaki, 2010, Tetrahedron Lett., 51, 3590, 10.1016/j.tetlet.2010.05.014 Panchenko, 2011, Mendeleev Commun., 21, 226, 10.1016/j.mencom.2011.07.019 Kuroiwa, 2008, Synlett., 2523 Tanabe, 2010, Chem. Lett., 39, 248, 10.1246/cl.2010.248 Yokota, 2007, Org. Lett., 9, 4639, 10.1021/ol702279w Ben-Daniel, 2003, J. Am. Chem. Soc., 125, 12116, 10.1021/ja0364524 Kobayashi, 2003, Tetrahedron, 59, 1547, 10.1016/S0040-4020(03)00047-4 Neimann, 2000, Org. Lett., 2, 2861, 10.1021/ol006287m Ravikumar, 1998, Eur. J. Org. Chem., 2937, 10.1002/(SICI)1099-0690(199812)1998:12<2937::AID-EJOC2937>3.0.CO;2-D Legros, 2002, Eur. J. Org. Chem., 3290, 10.1002/1099-0690(200210)2002:19<3290::AID-EJOC3290>3.0.CO;2-M Azzouzi-Zriba, 2011, J. Fluorine Chem., 132, 811, 10.1016/j.jfluchem.2011.05.018 Heydari, 2008, Synthesis, 19, 3126, 10.1055/s-2008-1067272 Heydari, 2009, Tetrahedron Lett., 50, 77, 10.1016/j.tetlet.2008.10.106 Heydari, 2009, J. Fluorine Chem., 130, 609, 10.1016/j.jfluchem.2009.03.014 Heydari, 2010, J. Fluorine Chem., 131, 106, 10.1016/j.jfluchem.2009.10.003 Khaksar, 2010, J. Fluorine Chem., 131, 1377, 10.1016/j.jfluchem.2010.10.002 Tajbakhsh, 2011, Synthesis, 490, 10.1055/s-0030-1258384 Sadanadam, 1987, Eur. J. Med. Chem., 22, 169, 10.1016/0223-5234(87)90015-8 Bonola, 1970, J. Med. Chem., 13, 329, 10.1021/jm00296a052 Hour, 2000, J. Med. Chem., 43, 4479, 10.1021/jm000151c Lee, 2010, Bull. Korean Chem. Soc., 31, 2451, 10.5012/bkcs.2010.31.9.2451 A. Alanine, L. C. Gobbi, S. Kolczewski, T. Luebbers, J. U. Peters, L. Steward, U.S. Patent US 2006293350 A1, 2006; Chem. Abstr. 146 (2006) 100721. P. V. Chaturvedula, L. Chen, R. Civiello, A. P. Degnan, G. M. Dubowchik, X. Han, X. J. Jiang, J. E. Macor, G. S. Poindexter, G. O. Tora, G. Luo, U.S. Patent US 2007149503 A1 (2007); Chem. Abstr. 147 (2007) 118256. Letourneau, 2006, Chem. Abstr, 145, 315012 Potewar, 2005, Synth. Commun., 35, 231, 10.1081/SCC-200048433 Armarego, 1979, Adv. Heterocycl. Chem., 24, 1, 10.1016/S0065-2725(08)60507-3 Segarra, 1998, Bioorg. Med. Chem. Lett., 8, 505, 10.1016/S0960-894X(98)00058-4 Akazome, 1995, J. Organomet. Chem., 494, 229, 10.1016/0022-328X(95)05387-5 Zeng, 2010, J. Heterocycl. Chem., 47, 1035, 10.1002/jhet.414 Venkat Lingaiah, 2006, Synlett., 2507 Lopez, 2000, J. Chem. Res. (S), 258, 10.3184/030823400103167381 Naleway, 1994, Tetrahedron Lett., 35, 8569, 10.1016/S0040-4039(00)78438-3 Mohammadpoor-Baltork, 2011, C. R. Chimie, 14, 944, 10.1016/j.crci.2011.05.003 Abdel-Jalil, 2004, Tetrahedron Lett., 45, 3475, 10.1016/j.tetlet.2004.03.003 Wang, 2006, Bull. Chem. Soc. Jpn., 79, 1426, 10.1246/bcsj.79.1426 Khosropour, 2006, Tetrahedron Lett., 47, 3561, 10.1016/j.tetlet.2006.03.079 Niknam, 2011, Chin. J. Chem., 29, 1417, 10.1002/cjoc.201180261 Rostamizadeh, 2010, Synthesis, 1356, 10.1055/s-0029-1218676 Zhang, 2010, J. Comb. Chem., 12, 643, 10.1021/cc100047j Chen, 2008, Tetrahedron Lett., 49, 3814, 10.1016/j.tetlet.2008.03.127 Narasimhulu, 2011, Tetrahedron, 67, 9627, 10.1016/j.tet.2011.08.018 Vuluga, 2011, J. Org. Chem., 76, 1126, 10.1021/jo1023816 Lu, 2001, Chem. Commun., 665, 10.1039/b100425p Iogansen, 1999, Spectrochim. Acta. (Part A), 55, 1585, 10.1016/S1386-1425(98)00348-5