Chemistry Heterocyclic Building Blocks Pyridines ethyl picolinate
Ambeed provide 41 derivatives of ethyl picolinate.
These compounds have the same murcko framework: ethyl picolinateEsterification: Ethyl picolinate can undergo esterification reactions with alcohols in the presence of acid catalysts to form various ethyl picolinates.
Hydrolysis: In the presence of strong acid or base, ethyl picolinate can undergo hydrolysis to yield picolinic acid and ethanol.
Transesterification: Ethyl picolinate can participate in transesterification reactions with other esters in the presence of suitable catalysts, resulting in the exchange of ester groups.
Nucleophilic substitution: Ethyl picolinate can undergo nucleophilic substitution reactions at the carbonyl carbon, leading to the formation of various substituted picolinates.
Reduction: Ethyl picolinate can be reduced to yield ethyl pyridine-2-carboxylate by using reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Oxidation: Ethyl picolinate can undergo oxidation reactions to form corresponding carboxylic acids or other oxidized products.
Condensation reactions: Ethyl picolinate can participate in condensation reactions with various reagents to form heterocyclic compounds or other organic products.
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Diethyl 4-hydroxypyridine-2,6-dicarboxylate
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Ethyl 6-(aminomethyl)picolinate hydrochloride
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Ethyl 3-chloro-5-(trifluoromethyl)picolinate
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Ethyl 5-amino-3-methoxypicolinate