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The Dimroth rearrangement is a rearrangement reaction taking place with certain 1,2,3-triazoles where endocyclic and exocyclic nitrogen atoms switch place.[1] This organic reaction was discovered in 1909 by Otto Dimroth.[2][3][4]
With R a phenyl group the reaction takes place in boiling pyridine for 24 hours.[5]
This type of triazole has an amino group in the 5 position. After ring-opening to a diazo intermediate, C-C bond rotation is possible with 1,3-migration of a proton.
Certain 1-alkyl-2-iminopyrimidines also display this type of rearrangement.
In the first step is an addition reaction of water followed by ring-opening of the hemiaminal to the aminoaldehyde followed by ring closure.
A known drug example of the Dimroth rearrangement includes in the synthesis of Bemitradine [88133-11-3].
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