Home Chemistry Heterocyclic Building Blocks Pyrimidines 5H-Pyrrolo[3,2-D]Pyrimidine
Substitution Reactions: If there are electrophilic or nucleophilic functional groups on the molecule, it can undergo substitution reactions. For example, it can undergo nucleophilic aromatic substitution (SNAr) or electrophilic aromatic substitution (SEAr) reactions.
Addition Reactions: Depending on the conditions, it can undergo addition reactions with electrophiles or nucleophiles. For instance, if it has a double bond, it might undergo addition reactions with electrophiles like halogens or nucleophiles.
Oxidation and Reduction Reactions: 5H-pyrrolo[3,2-d]pyrimidine can undergo oxidation or reduction reactions depending on the conditions and reagents used.
Ring-Opening Reactions: Under certain conditions, the pyrrolo[3,2-d]pyrimidine ring system can open, leading to the formation of open-chain compounds.
Cyclization Reactions: It can undergo intramolecular cyclization reactions if there are suitable functional groups that can form new rings within the molecule.
Halogenation: Depending on the presence of C-H bonds and the specific conditions, it can undergo halogenation reactions, where hydrogen atoms can be replaced by halogen atoms.
Amination: It can be aminated to introduce amino groups under appropriate reaction conditions.
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Ethyl 4-chloro-5H-pyrrolo[3,2-d]pyrimidine-6-carboxylate
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4-Chloro-6-methyl-5H-pyrrolo[3,2-d]pyrimidine
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4-Chloro-5H-pyrrolo[3,2-d]pyrimidin-2-amine
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4-Chloro-7-iodo-5H-pyrrolo[3,2-d]pyrimidine
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7-Bromo-2-chloro-5H-pyrrolo[3,2-d]pyrimidine
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4,7-Dichloro-5H-pyrrolo[3,2-d]pyrimidine
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4-Chloro-2-methyl-5H-pyrrolo[3,2-d]pyrimidine
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6-Bromo-4-chloro-5H-pyrrolo[3,2-d]pyrimidine
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