Chemistry Heterocyclic Building Blocks Pyridines 3-methoxypyridine
Ambeed provide 52 derivatives of 3-methoxypyridine.
These compounds have the same murcko framework: 3-methoxypyridineElectrophilic aromatic substitution: 3-Methoxypyridine can react with electrophiles such as acyl chlorides, acid anhydrides, or nitration reagents to substitute the methoxy group on the pyridine ring.
Nucleophilic substitution: The methoxy group in 3-methoxypyridine can be substituted by a nucleophile under suitable reaction conditions.
Oxidation: 3-Methoxypyridine can be oxidized to form pyridine N-oxide or other oxidation products under appropriate conditions.
Reduction: The pyridine ring or the methoxy group can be reduced to various products depending on the reagents and conditions used.
Alkylation/acylation: The nitrogen atom in the pyridine ring can undergo alkylation or acylation reactions with suitable alkylating or acylating agents.
Heterocyclic synthesis: 3-Methoxypyridine can participate in various heterocyclic synthesis reactions to form fused or spiro heterocyclic compounds.
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2-(5-Methoxypyridin-2-yl)acetonitrile
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5-Bromo-2-ethoxy-3-methoxypyridine
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(3-Methoxypyridin-4-yl)methanamine hydrochloride
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Potassium trifluoro(5-methoxypyridin-3-yl)borate
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Lithium triisopropoxy(5-methoxypyridin-2-yl)borate
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5-Methoxy-2-(trifluoromethyl)pyridine-4-carboxylic acid
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5-Methoxypicolinimidamide hydrochloride
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1-(5-Bromo-3-methoxypyridin-2-yl)ethanone
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4-(Chloromethyl)-3-methoxypyridine hydrochloride
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2-(5-Methoxypyridin-2-yl)ethanamine hydrochloride
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2-(Chloromethyl)-5-methoxypyridine hydrochloride
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6-Chloro-3-methoxy-2-nitropyridine