Home Chemistry Heterocyclic Building Blocks Oxadiazoles 3-Phenyl-1,2,4-Oxadiazole
Nucleophilic Substitution: The nitrogen atoms in the oxadiazole ring can serve as nucleophilic sites, undergoing substitution reactions with various electrophiles.
Reduction: The oxadiazole ring can be reduced using reducing agents like lithium aluminum hydride (LiAlH4) or hydrogen gas to yield the corresponding dihydro-1,2,4-oxadiazole.
Ring Opening: Under certain conditions, the oxadiazole ring can undergo ring-opening reactions to form different products, often involving nucleophiles or acids.
Halogenation: The phenyl ring can undergo halogenation reactions (e.g., bromination or chlorination) when treated with appropriate halogenating reagents.
N-alkylation or N-acylation: The nitrogen atoms in the oxadiazole ring can be alkylated or acylated using appropriate reagents.
Oxidation: The compound can undergo oxidation reactions under suitable conditions, potentially leading to the formation of new functional groups.
Heterocycle Formation: The oxadiazole can participate in heterocyclic reactions, forming fused or spirocyclic heterocyclic compounds when subjected to suitable reaction conditions.
Condensation Reactions: 3-Phenyl-1,2,4-oxadiazole can participate in various condensation reactions, such as the formation of imines or enamines.
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Ethyl 3-phenyl-1,2,4-oxadiazole-5-carboxylate
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5-Chloro-3-(4-chlorophenyl)-1,2,4-oxadiazole
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3,5-Difluoro-4-(5-isopropyl-1,2,4-oxadiazol-3-yl)phenol
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5-Chloro-3-(2-fluorophenyl)-1,2,4-oxadiazole
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3-(4-(Methylthio)phenyl)-1,2,4-oxadiazol-5-amine
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(3-(p-Tolyl)-1,2,4-oxadiazol-5-yl)methanamine hydrochloride
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Ethyl 3-(4-chlorophenyl)-1,2,4-oxadiazole-5-carboxylate
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4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid
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3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)benzoic acid
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4-(5-(Chloromethyl)-1,2,4-oxadiazol-3-yl)phenol
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2-(5-(Chloromethyl)-1,2,4-oxadiazol-3-yl)phenol
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3-(5-Ethyl-1,2,4-oxadiazol-3-yl)benzoic acid
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5-(Chloromethyl)-3-(4-fluorophenyl)-1,2,4-oxadiazole
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