Home Chemistry Heterocyclic Building Blocks Imidazoles 5,6,7,8-Tetrahydroimidazo[1,2-A]Pyrazine
Aromatic Reactions: 5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine contains an aromatic ring. It can undergo typical reactions of aromatic compounds, such as electrophilic aromatic substitution (EAS) reactions.
Nucleophilic Substitution: If there are suitable leaving groups or electrophilic sites, the compound can undergo nucleophilic substitution reactions.
Reduction: The compound may undergo reduction reactions, depending on the reagents and conditions. Reduction can lead to the formation of saturated rings or the reduction of other functional groups.
Oxidation: Oxidation reactions could be used to introduce additional functional groups or modify existing ones on the molecule.
Heterocyclic Chemistry: Since this compound contains two different heterocyclic rings, it can participate in a variety of reactions typical of heterocyclic chemistry. For example, it can react with various electrophiles and nucleophiles to form derivatives.
Metal-Catalyzed Reactions: Transition metal-catalyzed reactions, such as cross-coupling reactions, may be applicable to functionalize the compound.
Ring-Opening Reactions: Depending on the conditions and functional groups, ring-opening reactions might occur.
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tert-Butyl 5,6-dihydroimidazo[1,2-a]pyrazine-7(8H)-carboxylate
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7-Boc-3-bromo-5,6-dihydro-8H-imidazo[1,2-a]pyrazine
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tert-Butyl 2-(hydroxymethyl)-5,6-dihydroimidazo[1,2-a]pyrazine-7(8H)-carboxylate
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Ethyl 5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine-2-carboxylate hydrochloride
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7-tert-Butyl 2-ethyl 5,6-dihydroimidazo[1,2-a]pyrazine-2,7(8H)-dicarboxylate
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7-tert-Butyl 2-methyl 5,6-dihydroimidazo[1,2-a]pyrazine-2,7(8H)-dicarboxylate
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7-tert-Butyl 2-ethyl 3-bromo-5,6-dihydroimidazo[1,2-a]pyrazine-2,7(8H)-dicarboxylate
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2-(Trifluoromethyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine
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2-Ethyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine hydrochloride
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3-Methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine
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5,6,7,8-Tetrahydroimidazo[1,2-a]pyrazine hydrochloride
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