Home Chemistry Heterocyclic Building Blocks Pyridines 1-(Pyridin-3-Yl)Ethan-1-Amine
Nucleophilic substitution: The amino group can act as a nucleophile in substitution reactions. For example, it can react with alkyl halides to form N-alkylated products.
Acylation: The amino group can undergo acylation reactions with acyl halides or acid anhydrides to form amides.
Reduction: The pyridine ring can be reduced to piperidine under certain conditions, such as catalytic hydrogenation.
Alkylation: The pyridine nitrogen can be alkylated using alkyl halides under appropriate conditions.
Condensation reactions: The compound can undergo condensation reactions with carbonyl compounds to form imines or enamines.
Heterocyclization: The compound can participate in heterocyclization reactions to form fused or bridged heterocyclic compounds.
Protonation: The amine group can be protonated under acidic conditions, leading to the formation of a positively charged species.
Oxidation: Both the amine and the pyridine ring can be oxidized under suitable conditions to form respective oxidation products.
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(R)-1-(6-Chloropyridin-3-yl)ethan-1-amine dihydrochloride
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(S)-1-(5-Fluoropyridin-3-yl)ethan-1-amine
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(S)-1-(5-Chloropyridin-3-yl)ethanamine dihydrochloride
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(R)-1-(6-Chloropyridin-3-yl)ethanamine hydrochloride
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(R)-1-(6-Methoxypyridin-3-yl)ethan-1-amine dihydrochloride
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(1R)-1-[6-(trifluoromethyl)(3-pyridyl)]ethylamine
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(R)-1-(5-Bromopyridin-3-yl)ethanamine dihydrochloride
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(R)-1-(5-Bromopyridin-3-yl)ethanamine
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(R)-1-(5-Chloropyridin-3-yl)ethanamine
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(S)-1-(6-Chloropyridin-3-yl)ethan-1-amine dihydrochloride
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(S)-1-(6-Bromopyridin-3-yl)ethanamine hydrochloride
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(S)-1-(5-Fluoropyridin-3-yl)ethanamine hydrochloride
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(S)-1-(6-(Trifluoromethyl)pyridin-3-yl)ethan-1-amine
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