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DOI: 10.1055/s-2006-950219
8,9,10,10a-Tetrahydro-6H-tetrazolo[1,5-a]pyrrolo[2,1-c]pyrazines: New Heterocyclic Frameworks Generated by an Ugi-Type Multicomponent Reaction
Publikationsverlauf
Publikationsdatum:
04. September 2006 (online)

Abstract
A one-pot, Ugi-type three-component coupling process between an aldehyde, an isocyanide and proline tetrazole is reported, leading to new heterocyclic structures in good to excellent yields.
Key words
multicomponent reactions - heterocycles - tetrazole - Ugi reaction - proline derivatives
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1a
Armstrong RW.Combs AP.Tempest PA.Brown SD.Keating TA. Acc. Chem. Res. 1996, 29: 123 -
1b
Weber L.Illgen K.Almstetter M. Synlett 1999, 366 -
1c
Orru RVA.de Greef M. Synthesis 2003, 1471 -
1d
Zhu J. Eur. J. Org. Chem. 2003, 1133 -
1e
Ramón DJ.Yus M. Angew. Chem. Int. Ed. 2005, 44: 1602 - 2
Bienaymé H.Hulme C.Oddon G.Schmitt P. Chem. Eur. J. 2000, 6: 3321 - 3
Trost BM. Acc. Chem. Res. 2002, 35: 695 -
4a
Dömling A.Ugi I. Angew. Chem. Int. Ed. 2000, 39: 3168 -
4b
Dömling A. Curr. Opin. Chem. Biol. 2000, 4: 318 -
4c
Dömling A. Curr. Opin. Chem. Biol. 2002, 6: 306 -
4d
Ugi I.Werner B.Dömling A. Molecules 2003, 8: 53 -
4e
Dömling A. Chem. Rev. 2006, 106: 17 - 5
Ugi I.Meyr R.Fetzer U.Steinbrückner C. Angew. Chem. 1959, 71: 386 -
6a
Strocker AM.Keating TA.Tempest PA.Armstrong RW. Tetrahedron Lett. 1996, 37: 1149 -
6b
Keating TA.Armstrong RW. J. Am. Chem. Soc. 1996, 118: 2574 -
6c
Keating TA.Armstrong RW. J. Am. Chem. Soc. 1995, 117: 7842 -
6d
Mjalli AMM.Sarshar S.Baiga TJ. Tetrahedron Lett. 1996, 37: 2943 -
6e
Hulme C.Morrissette MM.Volz FA.Burns CJ. Tetrahedron Lett. 1998, 39: 1113 -
6f
Keating TA.Armstrong RW. J. Org. Chem. 1996, 61: 8935 -
6g
Rossen K.Sager J.DiMichele LM. Tetrahedron Lett. 1997, 38: 3183 -
6h
Ugi I.Rosendahl FK.Bodesheim F. Justus Liebigs Ann. Chem. 1963, 666: 54 -
6i
Ugi I. Angew. Chem., Int. Ed. Engl. 1962, 1: 8 -
6j
Kalinski C.Umkehrer M.Gonnard S.Jäger N.Ross G.Hiller W. Tetrahedron Lett. 2006, 47: 2041 -
6k
Ugi I. Angew. Chem., Int. Ed. Engl. 1982, 21: 810 -
6l
Nixey T.Kelly M.Hulme K. Tetrahedron Lett. 2000, 41: 8729 -
6m
Bienaymé H.Bouzid K. Tetrahedron Lett. 1998, 39: 2735 -
6n
Bossio R.Marcos CF.Marcaccini S.Pepino R. Tetrahedron Lett. 1997, 38: 2519 - For use of α-amino acids, see:
-
7a
Ugi I.Demharter A.Hörl W.Schmid T. Tetrahedron 1996, 52: 11657 -
7b
Ugi I.Hörl W.Hanusch-Kompa C.Schmid T.Herdtweck E. Heterocycles 1998, 47: 965 -
7c
Demharter A.Hörl W.Herdtweck E.Ugi I. Angew. Chem., Int. Ed. Engl. 1996, 35: 173 -
7d
Park SJ.Keum G.Kang SB.Koh HY.Kim Y.Lee DH. Tetrahedron Lett. 1998, 39: 7109 -
7e
Zimmer R.Ziemer A.Gruner M.Brüdgam I.Hartl H.Reissig H.-U. Synthesis 2001, 1649 -
7f
Kim YB.Choi EH.Keum G.Kang SB.Lee DH.Koh HY.Kim Y. Org. Lett. 2001, 3: 4149 -
7g
Godet T.Bonvin Y.Vincent G.Merle D.Thozet A.Ciufolini MA. Org. Lett. 2004, 6: 3281 - For use of β-amino acids, see:
-
8a
Pitlik J.Townsend CA. Bioorg. Med. Chem. Lett. 1997, 7: 3129 -
8b
Gedey S.Van der Eycken J.Fülöp F. Org. Lett. 2002, 4: 1967 - 9
Belinke D.Taube R.Illgen K.Nerdinger S.Herdtweck E. Synlett 2004, 688 - 12
Franckevičius V.Rahbek Knudsen K.Ladlow M.Longbottom DA.Ley SV. Synlett 2006, 889
References
In addition to the two usual isomers, reaction in methanol (Table [2] , entry 1) also afforded a racemic tetrazole decomposition product 30 (Figure [6] ), identity of which was confirmed by full characterisation, including an X-ray crystal structure (see reference 11).
Figure 6 Decomposition product 30
Crystallographic data (excluding structure factors) for the structures 20, 25 and 30 have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication nos. CCDC-612544, CCDC-612545 and CCDC-612546, respectively. Copies of the data can be obtained free of charge on application to the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK. [Fax: +44(1223)336033; E-mail: deposit@ccdc.cam.ac.uk].