Chemistry Heterocyclic Building Blocks Indoles 4-bromo-1H-indole
Ambeed provide 25 derivatives of 4-bromo-1H-indole.
These compounds have the same murcko framework: indole
Substitution Reactions: The bromine atom can undergo nucleophilic substitution reactions, where a nucleophile replaces the bromine. For example, substitution with a nucleophile such as an amine or an organometallic reagent can occur.
Suzuki-Miyaura Coupling: 4-bromo-1H-indole can participate in Suzuki-Miyaura coupling reactions with boronic acids or boronate esters, leading to the formation of biaryl compounds.
Lithiation: The bromine atom is a good leaving group, making 4-bromo-1H-indole suitable for lithiation reactions. This involves the replacement of the bromine with a lithium atom, generating a reactive intermediate that can be used in further reactions.
Bromination: 4-bromo-1H-indole can participate in bromination reactions, where the bromine atom is replaced by another halogen.
Metal-Catalyzed Reduction: The bromo group can be reduced to form the corresponding indole using metal-catalyzed hydrogenation or other reduction methods.
Arylation Reactions: 4-bromo-1H-indole can undergo palladium-catalyzed arylation reactions, introducing aryl groups at the bromine position.
Amidation: The bromo group can be converted to an amine group through amidation reactions, for example, by reacting with ammonia or amine derivatives.
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4-Bromo-6-(trifluoromethyl)-1H-indole
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Methyl 4-bromo-2-methyl-1H-indole-6-carboxylate