Chemistry Heterocyclic Building Blocks Pyridines 2-ethoxypyridine
Ambeed provide 20 derivatives of 2-ethoxypyridine.
These compounds have the same murcko framework: 2-ethoxypyridineSubstitution Reactions: The ethoxy group can undergo substitution reactions. For instance, it can be replaced by other functional groups under appropriate conditions. This could include reactions like nucleophilic substitution, where the ethoxy group is replaced by another nucleophile.
Electrophilic Aromatic Substitution (EAS): The pyridine ring in 2-ethoxypyridine can undergo EAS reactions. In this process, the electron-rich aromatic ring reacts with electrophiles. For example, it can react with nitration reagents to give nitro derivatives.
Alkylation and Acylation: The pyridine ring can also undergo alkylation or acylation reactions, where an alkyl or acyl group replaces a hydrogen atom on the ring. This could be achieved using appropriate alkylating or acylating agents.
Redox Reactions: 2-Ethoxypyridine can participate in redox reactions, either undergoing oxidation or reduction depending on the reaction conditions and the reagents involved.
Coordination Chemistry: The nitrogen atom in the pyridine ring can act as a ligand in coordination chemistry, forming complexes with transition metal ions.
Ring-closing Reactions: It may undergo ring-closing reactions under specific conditions, leading to the formation of cyclic compounds.
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(6-Ethoxy-5-fluoropyridin-3-yl)boronic acid
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(2-Ethoxypyridin-3-yl)boronic acid
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(6-Ethoxy-5-methylpyridin-3-yl)boronic acid
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(6-Ethoxy-4-methylpyridin-3-yl)boronic acid
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3-Bromo-2-ethoxy-5-(trifluoromethyl)pyridine