Chemistry Heterocyclic Building Blocks Pyridines 4-methoxypyridine
Ambeed provide 136 derivatives of 4-methoxypyridine.
These compounds have the same murcko framework: 4-methoxypyridineElectrophilic aromatic substitution reactions: The methoxy group can direct electrophilic aromatic substitution reactions at the ortho, meta, or para positions of the pyridine ring.
Nucleophilic substitution reactions: The pyridine nitrogen atom can undergo nucleophilic substitution reactions, especially with alkylating agents or acylating agents.
Oxidation reactions: The electron-rich nature of the pyridine ring makes it susceptible to oxidation reactions under appropriate conditions.
Reduction reactions: Depending on the reaction conditions and reagents used, 4-methoxypyridine can undergo reduction reactions, potentially reducing the pyridine ring or the methoxy group.
Functional group transformations: The methoxy group can undergo various functional group transformations, such as ether cleavage or substitution reactions.
Metal-catalyzed reactions: 4-methoxypyridine can participate in metal-catalyzed reactions, including cross-coupling reactions or metal-mediated functionalization reactions.
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(4-Methoxy-3-methylpyridin-2-yl)methanol
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5-Bromo-4-methoxynicotinaldehyde
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2-Chloro-4-methoxy-6-methyl-3-nitropyridine
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2-Chloro-4-methoxy-3-methylpyridine
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4-Methoxy-5-(trifluoromethyl)pyridin-2-amine
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5-Bromo-4-methoxy-2-(trifluoromethyl)pyridine
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2-(Chloromethyl)-4-methoxypyridine hydrochloride
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(6-Chloro-4-methoxypyridin-3-yl)methanol
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1-(4-Methoxypyridin-2-yl)ethan-1-amine
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2-(Bromomethyl)-4-methoxy-3,5-dimethylpyridine hydrobromide
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2-(Hydroxymethyl)-4-methoxy-3,5-dimethylpyridine 1-oxide
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Methyl 6-chloro-4-methoxy-2-methylnicotinate
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(4-Methoxypyridin-3-yl)boronic acid hydrochloride
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2-(Chloromethyl)-4-methoxy-3,5-dimethylpyridine