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Synthesis 2011(3): 463-468
DOI: 10.1055/s-0030-1258380
DOI: 10.1055/s-0030-1258380
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Dihydro-3H-chromeno-[3,4-b][4,7]phenanthrolin-3-one and Chromeno[4,3-b]pyrano[3,2-f]quinolin-3(13H)-one Derivatives by Aza-Diels-Alder Reaction
Further Information
Received
15 November 2010
Publication Date:
22 December 2010 (online)
Publication History
Publication Date:
22 December 2010 (online)
Abstract
Dihydro-3H-chromeno[3,4-b][4,7]phenanthrolin-3-one and chromeno[4,3-b]pyrano[3,2-f]quinolin-3(13H)-one derivatives have been synthesized by aza-Diels-Alder reaction of O-propargylated salicylaldehyde with 6-aminoquinolone and 6-aminocoumarin respectively. The reaction occurs in a single-step operation and provides potentially bioactive polycyclic heterocycles in high yields.
Key words
aza-Diels-Alder reaction - dihydro-3H-chromeno[3,4-b][4,7]phenanthrolin-3-one - chromeno[4,3-b]pyrano[3,2-f]quinolin-3(13H)-one - Lewis acid catalysis - annulated quinoline
-
1a
Elderfield RC. In Heterocyclic Compounds Vol. 4:Elderfield RC. Wiley; New York: 1960. Chap. 1. p.1 -
1b
Kournetsov VV.Mendez LYV.Gomez CMM. Curr. Org. Chem. 2005, 9: 141 -
1c
Bringmann G.Reichert Y.Kane V. Tetrahedron 2004, 60: 3539 -
1d
Sahu NS.Pal C.Mandal NB.Banerjee S.Raha M.Kundu AP.Basu A.Ghosh M.Roy K.Bandopadhyay S. Bioorg. Med. Chem. 2002, 10: 1687 -
1e
Campbell N. In Rodd’s Chemistry of Carbon Compounds Vol. IVf:Rodd EH. Elsevier; Amsterdam: 1976. p.231 - 2
Antimalarial
Drugs II
Peters W.Richards WHG. Springer Verlag; Berlin: 1984. -
3a
Maguire MP.Sheets KR.McVety K.Spada AP.Zilberstein A. J. Med. Chem. 1994, 37: 2129 -
3b
Kalluraya B.Sreenivasa S. Farmaco 1998, 53: 399 -
3c
Dube D.Blouin M.Brideau C.Chan C.-C.Desmarais S.Ethier D.Falgueyret J.-P.Friesen RW.Girard M.Girard Y.Guay J.Riendeau D.Tagari P.Young RN. Bioorg. Med. Chem. Lett. 1998, 8: 1255 -
3d
Roma G.Braccio MD.Grossi G.Mattioli F.Ghia H. Eur. J. Med. Chem. 2000, 35: 1021 -
3e
Benkovic SJ.Baker SJ.Alley MRK.Woo Y.-H.Zhang Y.-K.Akama T.Mao W.Baboval J.Rajagopalan PTR.Wall M.Kahng LS.Tavassoli A.Shapiro L. J. Med. Chem. 2005, 48: 7468 -
3f
Vargas LY.Castelli MV.Kouznetsov VV.Urbina JM.Lopez SN.Sortino M.Enriz RD.Ribas JC.Zacchino S. Bioorg. Med. Chem. 2003, 11: 1531 -
3g
Dassonneville L.Bonjean K.De Pauw-Gillet M.-C.Colson P.Houssier C.Quetin-Leclercq J.Angenot L.Ablordeppey SY. Bioorg. Med. Chem. 2002, 10: 1337 -
4a
Cassidy F.Evans JM.Hadley MS.Haladiji AH.Leach PE.Stemp G. J. Med. Chem. 1992, 35: 1623 -
4b
Atwal KS.Grover GJ.Ferrara FN.Ahmed SZ.Sleph PG.Dzwonczyk S.Normandin DE. J. Med. Chem. 1995, 38: 1966 -
4c
McKee TC.Fuller RW.Covington CD.Cardellina JH.Gulakowski RJ.Krepps BL.McMohon JB.Boyd MR. J. Nat. Prod. 1996, 59: 754 -
5a
Savouret JF.Chauchereau AE. Hum. Reprod. 1994, 9: 7 -
5b
Nies TW.Taylor AS. The Pharmacological Basis of Therapeutics 8th ed.: Pergamon Press; New York: 1990. Chap. 58. p.1397 - 6
Jones TK,Goldmani M. E,Hamman LG, andDavis RL. inventors; Patent WO 96/19458. -
7a
Michael JP. Nat. Prod. Rep. 2000, 17: 603 -
7b
Michael JP. Nat. Prod. Rep. 2004, 21: 650 -
8a
Marco JL.Carreiras MC. J. Med. Chem. 2003, 6: 518 -
8b
Puricelli L.Innocenti G.Delle Monache G.Caniato R.Filippini R.Cappelletti EM. Nat. Prod. Lett. 2002, 16: 95 -
8c
Corral RA.Orazi OO. Tetrahedron Lett. 1967, 7: 583 -
8d
Sekar M.Rejendra Prasad KJ.
J. Nat. Prod. 1998, 61: 294 -
9a
Swaminathan KS.Ganesh RS.Venkatachalam CS.Balasubramanian KK. Tetrahedron Lett. 1983, 24: 3653 -
9b
Ibrahim YA.Ahmed HM. J. Chem. Res., Synop. 1999, 254 -
9c
Tomashevskaya MM.Potekhin AA. Russ. J. Org. Chem. 2007, 43: 77 -
9d
Rabin B.Dhananjaya SNS.Ramu B.Sai UK.Rajender K.Mukkanti K.Pal M. Tetrahedron 2008, 64: 582 -
10a
Majumdar KC.Taher A.Sudipta P. Synlett 2010, 735 -
10b
Majumdar KC.Taher A.Debnath P. Synthesis 2009, 793 -
10c
Majumdar KC.Chattopadhyay B.Taher A. Synthesis 2007, 3647 - 11
Majumdar KC.Debnath P.Taher A. Lett. Org. Chem. 2008, 5: 169 - 12
Bashiardes G.Safir I.Barbot F.Laduranty J. Tetrahedron Lett. 2004, 45: 1567 -
13a
Baudelle R.Melnyk P.Deprez B.Tartar A. Tetrahedron 1998, 54: 4125 -
13b
Yamanaka M.Nishida A.Nakagana M. Org. Lett. 2000, 2: 159 -
13c
Deligny M.Carreaux F.Toupet L.Carboni B. Adv. Synth. Catal. 2003, 345: 1215 -
13d
Yadav JS.Reddy BVS.Sadashiv K.Padmavani B. Adv. Synth. Catal. 2004, 346: 607 -
13e
Berkessel A.Erturk E.Laporte C. Adv. Synth. Catal. 2006, 348: 223 -
14a
Majumdar KC.Taher A.Ray K. Tetrahedron Lett. 2009, 50: 3889 -
14b
Majumdar KC.Taher A.Ponra S. Tetrahedron Lett. 2010, 51: 147 -
14c
Majumdar KC.Taher A.Ponra S. Tetrahedron Lett. 2010, 51: 2297 -
14d
Jayashankaran J.Manian RDRS.Raghunathan R. Tetrahedron Lett. 2006, 47: 2265 -
14e
Matiychuk VS.Lesyk RB.Obushak MD.Gzella A.Atamanyuk DV.Ostapiuk YV.Kryshchyshyn AP. Tetrahedron Lett. 2008, 49: 4648 -
14f
Jimenez-Alonso S.Chavez H.Estevez-Braun A.Ravelo AG.Feresin G.Tapia A. Tetrahedron 2008, 64: 8938 -
14g
Lee YR.Kim YM.Kim SH. Tetrahedron 2009, 65: 101 -
14h
Ramesh E.Raghunathan R. Tetrahedron Lett. 2008, 49: 1812 -
14i
Khoshkholgh MJ.Balalaie S.Bijanzadeh HR.Gross JH. Synlett 2009, 55 -
14j
Khoshkholgh MJ.Balalaie S.Gleiter R.Rominger F. Tetrahedron 2008, 64: 10924 -
14k
Khoshkholgh MJ.Lotfi M.Balalaie S.Rominger F. Tetrahedron 2009, 65: 4228 -
15a
Beaudegnies R.Ghosez L. Tetrahedron: Asymmetry 1994, 5: 557 -
15b
Waldner A. Tetrahedron Lett. 1989, 30: 3061 -
15c
Tietze LF.Kettschau G. Top. Curr. Chem. 1997, 189: 1 - 16
Boger DL.Weinreb SN. Hetero Diels-Alder Methodology in Organic Synthesis Academic Press; San Diego: 1987. -
17a
Ramesh S.Gaddam V.Nagarajan R. Synlett 2010, 757 -
17b
Gaddam V.Ramesh S.Nagarajan R. Tetrahedron 2010, 66: 4218