Home Chemistry Heterocyclic Building Blocks Pyrimidines Thiazolo[5,4-D]Pyrimidine
Substitution Reactions: Thiazolo[5,4-d]pyrimidine can undergo substitution reactions with various electrophiles or nucleophiles, depending on the reaction conditions. For example, you can perform nucleophilic aromatic substitution (SNAr) or electrophilic aromatic substitution (SEAr) reactions.
Halogenation: Thiazolo[5,4-d]pyrimidine can be halogenated using reagents like bromine or chlorine to introduce halogen substituents onto the ring.
Acylation and Alkylation: Thiazolo[5,4-d]pyrimidine can undergo acylation and alkylation reactions with appropriate acylating or alkylating agents, leading to the introduction of acyl or alkyl groups on the ring.
Reduction: It can be subjected to reduction reactions to reduce any functional groups present, such as nitro groups to amino groups, using reducing agents like hydrogen and a catalyst or other reducing agents.
Oxidation: Depending on the reaction conditions, it may be oxidized to introduce oxygen-containing functional groups.
Cyclization Reactions: Thiazolo[5,4-d]pyrimidine can participate in intramolecular cyclization reactions, especially if it contains suitable functional groups, leading to the formation of fused or bridged ring systems.
Heterocyclic Chemistry: Since thiazolo[5,4-d]pyrimidine is itself a heterocyclic compound, it can participate in various reactions typical for heterocyclic compounds, such as ring-opening or ring-closing reactions.
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5,7-Dichloro-2-methylthiazolo[5,4-d]pyrimidine
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