Subscribe to RSS
DOI: 10.1055/s-0028-1088070
A Novel One-Pot, Three-Component Synthesis of 5-Imino-2,3,5,8-tetrahydropyrazolo[1,2-a]pyridazin-1-one Derivatives
Publication History
Publication Date:
27 April 2009 (online)
Abstract
It was found that the zwitterionic intermediate obtained from the addition of isocyanides to dimethyl acetylenedicarboxylate could react with 1,3-dipolar compounds under mild conditions to produce 5-imino-2,3,5,8-tetrahydropyrazolo[1,2-a]pyridazin-1-one derivatives in high yields. A plausible mechanism was also discussed for this process.
Key words
isocyanide - dimethyl acetylenedicarboxylate - multicomponent reactions - 1,3-dipolar compounds - 5-imino-2,3,5,8-tetrahydropyrazolo[1,2-a]pyridazin-1-one
- 1
Ugi I. Angew. Chem., Int. Ed. Engl. 1982, 21: 810 - 2
Dömling A. Chem. Rev. 2006, 106: 17 - 3
Dömling A.Ugi I. Angew. Chem. Int. Ed. 2000, 39: 3168 - 4
Ahmadi E.Ramazani A.Haghighi M. N. Tetrahedron Lett. 2007, 48: 6954 - 5
Zinner G.Moderhack D.Kliegel W. Chem. Ber. 1969, 102: 2536 -
6a
Nair V.Nair JS.Vinod AU.Rath NP. J. Chem. Soc., Perkin Trans. 1 1997, 3129 -
6b
Nair V.Nair JS.Vinod AU. Synthesis 2000, 1713 -
6c
Nair V.Bindu S.Balgopal L. Tetrahedron Lett. 2001, 42: 2043 -
6d
Nair V.Vinod AU. Chem. Commun. 2000, 1019 - 7
Yadav JS.Reddy SBV.Shubashree S.Shadiv K.Naidu JJ. Synthesis 2004, 2376 -
8a
Nair V.Vinod AU. J. Org. Chem. 2001, 66: 4427 -
8b
Nair V.Vinod AU.Nair JS.Sreekanth AR.Rath NP. Tetrahedron Lett. 2000, 41: 6675 -
8c
Nair V.Vinod AU.Ramesh R.Menon RS.Varma RL.Mathew S.Chiaroni A. Heterocycles 2002, 58: 147 -
8d
Nair V.Mathen JS.Vinod AU.Varma RL. Chem. Lett. 2001, 30: 738 -
9a
Yavari I.Adib M.Sayahi MH. J. Chem. Soc., Perkin Trans. 1 2002, 2343 -
9b
Yavari I.Nasiri F.Moradi L.Djahaniani H. Tetrahedron Lett. 2004, 45: 7099 - 10
Winterfeldt E.Schumann D.Dillinger HJ. Chem. Ber. 1969, 102: 1656 - 11
Adib M.Koloogani SA.Abbasi A.Bijanzadeh HR. Synthesis 2007, 3056 - 13
Adib M.Sayahi MH.Rahbari S. Tetrahedron Lett. 2005, 46: 6545 - 14
Walborsky HM.Periasamy MP. In The Chemistry of Functional Groups, Supplement CPatai S.Rappaport Z. Wiley; New York: 1983. Chap. 20. p.835-837 -
16a
Hosseini-Sarvari M.Sharghi H. J. Org. Chem. 2006, 71: 6652 -
16b
Janza B.Studer A. Org. Lett. 2006, 8: 1875 -
17a
Taylor EC.Haley NF.Clemens RJ. J. Am. Chem. Soc. 1981, 103: 7743 -
17b
Perri ST.Slater SC.Toske SG.White JD. J. Org. Chem. 1990, 55: 6037 -
17c
Shintani R.Fu GC. J. Am. Chem. Soc. 2003, 125: 10778 -
17d
Suárez A.Downey CW.Fu GC. J. Am. Chem. Soc. 2005, 127: 11244 -
17e
Shintani R.Hayashi T. J. Am. Chem. Soc. 2006, 128: 6330 -
17f
Sibi MP.Stanley LM.Nie X.Venkatraman L.Liu M.Jasperse CP. J. Am. Chem. Soc. 2007, 129: 395
References
The atomic coordinates for 4a have been deposited at the Cambridge Crystallographic Data Centre (deposition number CCDC 702357). The coordinates can be obtained on request from the Director Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK, e-mail: deposit@ccdc.cam.ac.uk, fax: +44(1223)336033.
15The atomic coordinates for 8 have been deposited at the Cambridge Crystallographic Data Centre (deposition number CCDC 713140). The coordinates can be obtained on request from the Director Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK, e-mail: deposit@ccdc.cam.ac.uk, fax: +44(1223)336033.