Home Chemistry Heterocyclic Building Blocks Oxazines 2H-Pyrido[3,2-B][1,4]Oxazin-3(4H)-One
Substitution Reactions: The oxazin-3-one ring can undergo substitution reactions, such as nucleophilic substitution, where a nucleophile can attack the carbonyl group. For example, you can perform nucleophilic acylation to replace the oxygen atom with another nucleophile.
Reduction Reactions: The carbonyl group (C=O) can be reduced to form a hydroxyl group (C-OH) using reducing agents like sodium borohydride or lithium aluminum hydride.
Cyclization Reactions: Depending on the reaction conditions, it's possible to perform intramolecular cyclization reactions to form other heterocyclic compounds.
Condensation Reactions: You can perform condensation reactions to link this compound with other molecules or reagents to create larger compounds with extended conjugated systems.
Oxidation Reactions: Depending on the specific substituents and reaction conditions, oxidation reactions can be applied to transform this compound into other products.
Hydrolysis: Under appropriate conditions, you can perform hydrolysis reactions to cleave the oxazin-3-one ring and produce simpler compounds.
Nucleophilic Addition: Nucleophiles can attack the carbon-carbon double bond in the pyrido ring or the oxazin ring, leading to various addition reactions.
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7-Bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one
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6-Nitro-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one
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2,2-Dimethyl-6-nitro-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one
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6-Amino-2,2-dimethyl-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one
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6-Bromo-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one
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2,2-Dimethyl-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one
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