Home Chemistry Heterocyclic Building Blocks Pyridines 1-(Pyridin-4-Yl)Ethan-1-Amine
Acylation: The amine group can undergo acylation reactions with acid chlorides or acid anhydrides to form amides.
Alkylation: The amine group can undergo alkylation reactions with alkyl halides or sulfonates to form N-alkylated products.
Reductive Amination: The amine group can participate in reductive amination reactions, where it reacts with a carbonyl compound (like an aldehyde or ketone) and a reducing agent (like NaBH4 or a metal catalyst) to form secondary or tertiary amines.
Nucleophilic Substitution: The nitrogen atom of the pyridine ring can act as a nucleophile in substitution reactions with electrophiles, such as alkyl halides or acyl chlorides.
Heterocyclization: The pyridine ring can undergo various cyclization reactions, leading to the formation of heterocyclic compounds under appropriate conditions.
Oxidation: The amine group or the carbon adjacent to the nitrogen can undergo oxidation reactions under certain conditions, forming imines or oximes.
Condensation: The amine group can undergo condensation reactions with carbonyl compounds to form imines or Schiff bases.
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(S)-1-(2-Methoxypyridin-4-yl)ethanamine dihydrochloride
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(S)-1-(2-Methoxypyridin-4-yl)ethanamine hydrochloride
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(S)-1-(2-Methoxypyridin-4-yl)ethanamine
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1-(Pyridin-4-yl)ethanamine dihydrochloride
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1-(2-Chloropyridin-4-yl)ethan-1-amine dihydrochloride
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1-(2-Methylpyridin-4-yl)ethan-1-amine dihydrochloride
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1-(2-Methoxypyridin-4-yl)ethan-1-amine dihydrochloride
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1-(2-(Trifluoromethyl)pyridin-4-yl)ethanamine dihydrochloride
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1-(2-(Trifluoromethyl)pyridin-4-yl)ethanamine hydrochloride
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(R)-1-(2-Chloropyridin-4-yl)ethan-1-amine dihydrochloride
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(R)-1-(2-Chloropyridin-4-yl)ethan-1-amine
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(S)-1-(2-Bromopyridin-4-yl)ethanamine dihydrochloride
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(S)-1-(2-Chloropyridin-4-yl)ethanamine dihydrochloride
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(S)-1-(2-Chloropyridin-4-yl)ethanamine
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