Home Chemistry Heterocyclic Building Blocks Pyridines 3-Bromo-4-Methylpyridine
Substitution reactions: The bromine atom can undergo substitution reactions with various nucleophiles, such as amines or alkoxides, leading to the displacement of the bromine atom with the nucleophile.
Metalation reactions: The pyridine ring can undergo metalation reactions with strong bases, leading to the formation of metal complexes or organometallic compounds.
Oxidation reactions: The methyl group can undergo oxidation under certain conditions, leading to the formation of carboxylic acids, ketones, or aldehydes.
Reduction reactions: The bromine atom or the pyridine ring can undergo reduction reactions, depending on the conditions and reagents used.
Cross-coupling reactions: The bromine atom can participate in cross-coupling reactions with suitable partner molecules, such as organometallic reagents, to form biaryl or heteroaryl compounds.
Ring-closure reactions: Under appropriate conditions, the compound can undergo ring-closure reactions to form cyclic compounds, such as azepines or piperidines.
Functional group transformations: Various functional group transformations, such as halogenation, alkylation, or acylation, can occur depending on the reagents and conditions employed.
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(R)-1-(5-Bromo-4-methylpyridin-2-yl)ethan-1-amine dihydrochloride
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2-((5-Bromo-4-methylpyridin-2-yl)amino)ethanol
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N-(5-Bromo-4-methylpyridin-2-yl)acetamide
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5-Bromo-4-methyl-2-(methylsulfonyl)pyridine
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5-Bromo-4-methyl-2-(trifluoromethyl)pyridine
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5-Bromo-4-methyl-2-(propan-2-yl)pyridine
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(S)-1-(5-Bromo-4-methylpyridin-2-yl)ethanamine dihydrochloride
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1-(5-Bromo-4-methylpyridin-2-yl)ethanone
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