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- Imidazo[1,2-A]Pyridine, 3,5-Dibromo-
- 3,5-Dibromoimidazo[1,2-a]pyridine
The synthesis of 3,5-dibromoimidazo[1,2-a]pyridine by nitro group reduction with sodium methoxide and reductive elimination with ethanol is shown in the following scheme. The first step is the formation of a nitro group from 2-bromopyridine in the presence of nitric acid and acetic anhydride. Methoxide anion then reduces the nitro group to form 3-bromopyridine. Ethanol is added to the reaction mixture to eliminate hydrogen bromide and form 3,5-dibromoimidazo[1,2-a]pyridine.
3,5-Dibromoimidazo[1,2-a]pyridine can be synthesized from 2-bromopyridine via a two step process consisting of nitro group reduction followed by reductive elimination. In the first step of this process 2-bromop
Chemical properties
Technical inquiry about: 3D-UCA21412 3,5-Dibromoimidazo[1,2-a]pyridine
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