Fischer Indole Synthesis

Fischer Indole Synthesis

27 August, 2014 / by / in Reactions
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  • Generality
  • Reagent Availability
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  • Criteria #4
  • Criteria #5

  • General Characteristics

Upon heating under acidic conditions, aryl hydrazones synthesized from aldehydes/ketones and aryl hydrazines undergo sigmatropic rearrangement and aromatization to give substituted indole products.

This vintage Fischer indole synthesis is a highly general, standard way to synthesize indole-containing alkaloids and drug molecules.

One of the contemporary modified versions uses the Buchwald-Hartwig coupling to synthesize aryl hydrazones from aryl halides and alkyl hydrazones (the Buchwald modification).

fischer_indole_4.gif

  • General References

・Fischer, E.; Jourdan, F. Ber. 1883, 16, 2241.
・Fischer, E.; Hess, O. Ber. 1884, 17, 559.
・Miyata, O.; Kimura, Y.; Muroya, K.; Hiramatsu, H.; Naito, T. Tetrahedron Lett. 1997, 62, 425. DOI: 10.1016/S0040-4039(99)00583-3

<Buchwald Modification>
・Wagaw, S.; Yang, B. H.; Buchwald, S. L. J. Am. Chem. Soc. 1998, 120, 6621. DOI: 10.1021/ja981045r
・Wagaw, S.; Yang, B. H.; Buchwald, S. L. J. Am. Chem. Soc. 1999, 121, 10251. DOI: 10.1021/ja992077x

<Reviews>
・Van Orden, R. B.; Lindwell, H. G. Chem. Rev. 1942, 30, 69. DOI: 10.1021/cr60095a004
・Robinson, B. Chem. Rev. 1963, 63, 373. DOI: 10.1021/cr60224a003
・Robinson, B. Chem. Rev. 1969, 69, 227. DOI: 10.1021/cr60258a004
・Robinson, B. “The Fischer Indole Synthesis”, John Wiley & Sons Inc., New York, 1982.
・Inman, M.; Moody, C. Chem. Sci. 2012, doi:10.1039/C2SC21185H

 

  • Reaction Mechanism

fisher.jpg

  • Examples

The total synthesis of peduncularine.[1]

fischer_indole_3.gif

The synthesis of indometacin.

fischer_indole_2.gif

An application to the complex substrates in the total synthesis of haplophytine.[2]

fischer_indole_5.gif

An interesting example of catalytic asymmetric Fischer indole synthesis.[3]

fischer_indole_7.gif

  • Experimental Procedure

  • Experimental Tips

  • References

[1] Roberson, C. W.; Woerpel, K. A, J. Am. Chem. Soc. 2002, 124, 11342. DOI: 10.1021/ja012152f
[2] Ueda, H.; Satoh, H.; Matsumoto, K.; Sugimoto, K.; Fukuyama, T.; Tokuyama, H. Angew. Chem. Int. Ed. 2009, 48, 7600. doi: 10.1002/anie.200902192
[3] Muller, S.; Webber, M. J.; List, B. J. Am. Chem. Soc. 2011, 133, 18534. DOI: 10.1021/ja2092163

  • Related Books

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