Synthesis 2011(11): 1711-1716  
DOI: 10.1055/s-0030-1260044
PAPER
© Georg Thieme Verlag Stuttgart ˙ New York

One-Pot Synthesis of 9H-Indolo[3,2-c]pyrazolo[1,5-a]quinolines, 1H-Dipyrazolo[1,5-a:4′,3′-c]quinolines and 1H-Imidazo[4,5-c]pyrazolo[1,5-a]quinolines: Three New Heterocyclic Systems

Yiming Zhang, Ren Wang, Zongjun Shi, Wei Zhang*
State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P. R. of China
Fax: +86(931)8625657; e-Mail: zhangwei6275@lzu.edu.cn;
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Publikationsverlauf

Received 14 February 2011
Publikationsdatum:
16. Mai 2011 (online)

Abstract

An efficient synthesis of three new kinds of heterocyclic systems, 9H-indolo[3,2-c]pyrazolo[1,5-a]quinolines, 1H-dipyrazolo[1,5-a:4′,3′-c]quinolines and 1H-imidazo[4,5-c]pyrazolo[1,5-a]quinolines, has been achieved by the photochemical oxidative dehydrogenation and subsequent photocyclization and dehydrochlorination of 5-(2-chloro-1H-indol-3-yl)-, 5-(5-chloro-1H-pyrazol-4-yl)- and 5-(5-chloro-1H-imidazol-4-yl)-1-phenyl-4,5-dihydro-1H-pyrazoles in the presence of pyridine in acetone.

    References

  • 1a Mallory FB. Mallory CW. Org. React. (N.Y.)  1984,  30:  1 
  • 1b Laarhoven WH. Org. Photochem.  1989,  10:  163 
  • 1c Meier HT. Angew. Chem., Int. Ed. Engl.  1992,  31:  1399 
  • 1d Lewis FD. Kalgutkar RS. Yang J.-S. J. Am. Chem. Soc.  2001,  123:  3878 
  • 1e Neo AG. Lopez C. Romero V. Antelo B. Delamano J. Perez A. Fernandez D. Almeida JF. Castedo L. Tojo G. J. Org. Chem.  2010,  75:  6764 
  • 1f Moulton BE. Dong H. O’Brien CT. Duckett SB. Lin Z. Fairlamb IJS. Org. Biomol. Chem.  2008,  6:  4523 
  • 2a Austin M. Egan OJ. Tully R. Pratt AC. Org. Biomol. Chem.  2007,  5:  3778 
  • 2b Hewlins MJE. Salter R. Synthesis  2007,  2164 
  • 2c Abbate S. Bazzini C. Caronna T. Fontana F. Gambarotti C. Gangemi F. Longhi G. Mele A. Sora IN. Panzeri W. Tetrahedron  2006,  62:  139 
  • 2d Link JT. Raghavan S. Danishefsky SJ. J. Am. Chem. Soc.  1995,  117:  552 
  • 3a Olsen RJ. Pruett SR. J. Org. Chem.  1985,  50:  5457 
  • 3b Giles RGF. Sargent MV. J. Chem. Soc., Chem. Commun.  1974,  215 
  • 3c Wood CS. Mallory FB. J. Org. Chem.  1964,  29:  3373 
  • 4a Reddy GM. Chen S.-Y. Uang B.-J. Synthesis  2003,  497 
  • 4b Suzuki H. Aoyagi S. Kibayashi C. Tetrahedron Lett.  1995,  36:  935 
  • 4c Berlinck RGS. Britton R. Piers E. Lim L. Roberge M. Moreira da Rocha R. Andersen RJ. J. Org. Chem.  1998,  63:  9850 
  • 4d Gallant M. Link JT. Danishefsky SJ. J. Org. Chem.  1993,  58:  343 
  • 4e Kobayashi Y. Fujimoto T. Fukuyama T. J. Am. Chem. Soc.  1999,  121:  6501 
  • 5a Fröhner W. Monse B. Braxmeier TM. Casiraghi L. Sahagún H. Seneci P. Org. Lett.  2005,  7:  4573 
  • 5b Engler TA. Furness K. Malhotra S. Sanchez-Martinez C. Shih C. Xie W. Zhu G. Zhou X. Conner M. Faul MM. Sullivan KA. Kolis SP. Brooks HB. Patel B. Schultz RM. DeHahn TB. Kirmani K. Spencer CD. Watkins SA. Considine EL. Dempsey JA. Ogg CA. Stamm NB. Anderson BD. Campbell RM. Vasudevan V. Lytle ML. Bioorg. Med. Chem. Lett.  2003,  13:  2261 
  • 5c Messaoudi S. Anizon F. Peixoto P. David-Cordonnier M. Bioorg. Med. Chem.  2006,  14:  7551 
  • 5d Routier S. Ayerbe N. Mérour J.-Y. Coudert G. Bailly C. Pierré A. Pfeiffer B. Caignard D.-H. Renard P. Tetrahedron  2002,  58:  6621 
  • 5e Thompson JE. Cubbon RM. Cummings RT. Wicker LS. Frankshun R. Cunningham BR. Cameron PM. Meinke PT. Liverton N. Weng Y. DeMartino JA. Bioorg. Med. Chem. Lett.  2002,  12:  1219 
  • 6 Lu S. Zhang W. Pan J. Zhang J. Synthesis  2008,  1517 
  • 7a Barrett D. Recent Res. Dev. Org. Chem.  1997,  1:  137 
  • 7b Barrett D. Sasaki H. Kinoshita T. Fujikawa A. Sakane K. Tetrahedron  1996,  52:  8471