pyridin-3-ylmethanamine-Pyridines| Ambeed

: Nitrosation: The pyrimidine ring can be nitrosated with nitrous acid to form the corresponding nitroso compound. Alkylation: 1H-pyrazolo[4,3-d]pyrimidine can undergo alkylation reactions, where alkyl groups are introduced onto the nitrogen atoms or other suitable positions in the molecule. Amination: Amination reactions can be carried out to introduce amino groups onto the pyrazolo[4,3-d]pyrimidine ring system. Halogenation: Halogenation reactions, such as bromination or chlorination, can be used to introduce halogen atoms onto the pyrazole or pyrimidine rings. Reduction: The nitro group, if present, can be reduced to an amino group using reducing agents like hydrogen and a catalyst. Cyclization: Depending on the reaction conditions and substituents, 1H-pyrazolo[4,3-d]pyrimidine can undergo intramolecular cyclization reactions to form fused heterocyclic compounds. Oxidation: Oxidation reactions can be employed to convert certain functional groups within the molecule, such as sulfides to sulfoxides or sulfones. Nucleophilic substitution: If suitable leaving groups are present, nucleophilic substitution reactions can occur at specific positions in the molecule.

$1421.00/25g