Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
Synthesis 2010(20): 3536-3544
DOI: 10.1055/s-0030-1258195
DOI: 10.1055/s-0030-1258195
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
A Facile Route to 1,3-Diazaheterocycle-Fused [1,2-a]Indole Derivatives via Acetic Acid Catalyzed Cyclocondensation Reactions
Further Information
Received
7 June 2010
Publication Date:
04 August 2010 (online)
Publication History
Publication Date:
04 August 2010 (online)
Abstract
A concise and efficient route for the synthesis of 1,3-diazaheterocycle-fused [1,2-a]indoles by simply refluxing a reaction mixture of different types of heterocyclic ketene aminals and 1,4-benzoquinones catalyzed by acetic acid was developed. This protocol provides an alternative method for application in combinatorial and parallel synthesis in drug discovery.
Key words
1,3-diazaheterocycle-fused [1,2-a]indoles - heterocyclic ketene aminals - 1,4-benzoquinones - catalyst - acetic acid
-
2a
Numata A.Takahashi C.Matsushita T.Miyamoto T.Kawai K.Usami Y.Matsumura E.Inoue M.Ohishi H.Shingu T. Tetrahedron Lett. 1992, 33: 1621 -
2b
Takahashi C.Matsushita T.Doi M.Minoura K.Shingu T.Kumeda Y.Numata A. J. Chem. Soc., Perkin Trans. 1 1995, 2345 -
2c
Barrow CJ.Sun HH. J. Nat. Prod. 1994, 57: 471 -
2d
de la Mora MA.Cuevas E.Muchowski JM.Cruz-Almanza R. Tetrahedron Lett. 2001, 42: 5351 -
3a
Goetz MA.Lopez M.Monaghan RL.Chang RSL.Lotti VJ.Chen TB. J. Antibiot. 1985, 36: 1633 -
3b
Liesch JM.Hensens OD.Springer JP.Chang RSL.Lotti VJ. J. Antibiot. 1985, 36: 1638 -
3c
Sun HH.Byard SJ.Cooper R. J. Antibiot. 1994, 47: 599 - 4
Wong SM.Musza LL.Kydd GC.Kullnig R.Gillum AM.Cooper R. J. Antibiot. 1993, 46: 545 - 5
Snider BB.Zeng H. J. Org. Chem. 2003, 68: 545 -
6a
Kost AN.Golubeva GA.Portnov YN. Dokl. Akad. Nauk USSR 1971, 200: 342 ; Chem. Abstr. 1972, 76, 34047 -
6b
Portnov YN.Golubeva GA.Kost AN. Khim. Geterotsikl. Soedin. 1972, 61 ; Chem. Abstr. 1972, 77, 448377 -
6c
Portnov YN.Golubeva GA.Kost AN.Volkov VS. Khim. Geterotsikl. Soedin. 1973, 647 ; Chem. Abstr. 1973, 79, 453269 -
6d
Coppola EM.Hardtmann GE. J. Heterocycl. Chem. 1979, 16: 769 -
6e
Sutherland JK. Chem. Commun. 1997, 325 - 7
Yuen J.Fang YQ.Lautens M. Org. Lett. 2006, 8: 653 - 8
He F.Foxman BM.Snider BB. J. Am. Chem. Soc. 1998, 120: 6417 -
9a
Snider BB.Zeng H. Org. Lett. 2002, 4: 1087 -
9b
Snider BB.Zeng H. Org. Lett. 2000, 2: 4103 -
10a
Zhang J.-H.Wang M.-X.Huang Z.-T. J. Chem. Soc., Perkin Trans. 1 1999, 321 -
10b
Yu C.-Y.Yang P.-H.Zhao M.-X.Huang Z.-T. Synlett 2006, 1835 -
10c
Liao J.-P.Zhang T.Yu C.-Y.Huang Z.-T. Synlett 2007, 761 - For previous reviews, see:
-
10d
Huang Z.-T.Wang M.-X. Heterocycles 1994, 37: 1233 -
10e
Huang Z.-T.Wang M.-X. Prog. Nat. Sci. 1999, 11: 971 -
11a
Tieman CH,Kollmeyer WD, andRoman SA. inventors; German Patent 2445421. ; Chem. Abstr. 1975, 83, 97297h -
11b
Tieman CH, andKollmeyer WD. inventors; US Patent 3948934. ; Chem. Abstr. 1976, 85, 46680e -
11c
Porter PE, andKollmeyer WD. inventors; US Patent 4053623. ; Chem. Abstr. 1977, 87, 37796g -
12a
Maryanoff BE.Nortey SO.McNally JJ.Sanfilippo PJ.McComsey DF.Dubinsky B.Shank RP.Reitz AB. Biomed. Chem. Lett. 1999, 9: 1547 -
12b
Kondo H.Taguchi M.Inoue Y.Sakamoto F.Tsukamoto G. J. Med. Chem. 1990, 33: 2012 - 13
Suryawanshi SN.Pandey S.Rashmirathi Bhatt BA.Gupta S. Eur. J. Med. Chem. 2007, 42: 511 - 14
Abdelhalim MM.El-Saidi MMT.Rabie ST.Elmegeed GA. Steroids 2007, 72: 459 -
15a
Yan S.-J.Huang C.Su C.-X.Ni Y.-F.Lin J. J. Comb. Chem. 2010, 12: 91 -
15b
Yan S.-J.Niu Y.-F.Huang R.Lin J. Synlett 2009, 2821 - 16
Aggarwal V.Kumar A.Ila H.Junjappa H. Synthesis 1981, 157 - 18
Zhao M.-X.Wang M.-X.Huang Z.-T. Tetrahedron 2002, 58: 1309 -
19a
Huang Z.-T.Wang M.-X. Synthesis 1992, 1273 -
19b
Li Z.-J.Charles D. Synth. Commun. 2001, 31: 527
References
These authors contributed equally to this paper.
17CCDC 777124 contains the supplementary crystallographic data for compound 3a. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.