Chemistry Heterocyclic Building Blocks Indazoles 6-bromo-1H-indazole
Ambeed provide 23 derivatives of 6-bromo-1H-indazole.
These compounds have the same murcko framework: 6-bromo-1H-indazoleSubstitution Reactions: The bromine atom can undergo nucleophilic substitution reactions, such as displacement by a nucleophile, leading to the formation of various substituted indazoles.
Metalation: The indazole ring can undergo metalation reactions with strong bases, leading to the formation of organometallic compounds.
Cross-Coupling Reactions: The bromine atom can participate in palladium-catalyzed cross-coupling reactions, such as Suzuki coupling or Heck reaction, to introduce diverse substituents onto the indazole ring.
Reduction: The bromine atom can be reduced to a bromide ion or replaced by a hydrogen atom under appropriate conditions, leading to the formation of a reduced product.
Grignard Reaction: The indazole ring can react with a Grignard reagent to form a new carbon-carbon bond, leading to the introduction of various functional groups.
Nucleophilic Aromatic Substitution: The bromine atom can undergo nucleophilic aromatic substitution reactions with strong nucleophiles, leading to substitution of the bromine atom by the nucleophile.
Halogenation: The indazole ring can undergo halogenation reactions, such as bromination or chlorination, under appropriate conditions to introduce halogen substituents.
Cyclization Reactions: Depending on the reaction conditions, 6-bromo-1H-indazole can participate in cyclization reactions to form fused or spirocyclic compounds.
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6-Bromo-3-(trifluoromethyl)-1H-indazole
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Ethyl 6-bromo-1H-indazole-3-carboxylate
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6-Bromo-5-(trifluoromethoxy)-1H-indazole