Fischer indole synthesis
Chemical reaction
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Through Chemical reaction, Aromaticity and Aldehyde
This reaction can be catalyzed by Brønsted acids such as HCl, H2SO4, polyphosphoric acid and p-toluenesulfonic acid or Lewis acids such as boron trifluoride, zinc chloride, and aluminium chloride.
Several reviews have been published.
Reaction mechanism
The reaction of a (substituted) phenylhydrazine with a carbonyl (aldehyde or ketone) initially forms a phenylhydrazone which isomerizes to the respective enamine (or 'ene-hydrazine'). After protonation, a cyclic [3,3]-sigmatropic rearrangement occurs producing a diimine. The resulting diimine forms a cyclic aminoacetal (or aminal), which under acid catalysis eliminates NH3, resulting in the energetically favorable aromatic indole.
Isotopic labelling studies show that the aryl nitrogen (N1) of the starting phenylhydrazine is incorporated into the resulting indole.
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Buchwald modification
Via a palladium-catalyzed reaction, the Fischer indole synthesis can be effected by cross-coupling aryl bromides and hydrazones. This result supports the previously proposed intermediacy as hydrazone intermediates in the classical Fischer indole synthesis. These N-arylhydrazones undergo exchange with other ketones, expanding the scope of this method.
Application
- A variant of the Fischer indolization reaction, termed the interrupted Fischer indolization by Garg and coworkers, has been used in the total synthesis of akuammiline natural products. The method has also been used in medicinal chemistry.
- Indometacin preparation.
- Triptan synthesis
- Iprindole synthesis (phenylhydrazine + suberone → 2,3-Cycloheptenoindole).