1H-pyrazolo[3,4-b]pyrazine-Pyrazines| Ambeed

Chemistry Heterocyclic Building Blocks Pyrazines 1H-pyrazolo[3,4-b]pyrazine

1H-pyrazolo[3,4-b]pyrazine

Ambeed provide 5 derivatives of 1H-pyrazolo[3,4-b]pyrazine.

These compounds have the same murcko framework: 1H-pyrazolo[3,4-b]pyrazine.

Arylation or Alkylation: You can introduce substituents at various positions on the pyrazine rings through reactions like Friedel-Crafts acylation or alkylation.
Oxidation: 1H-pyrazolo[3,4-b]pyrazine can be oxidized under certain conditions to produce various oxidized derivatives.
Reduction: Reduction reactions can be performed to reduce the compound to its corresponding dihydro form or even to more reduced derivatives.
Halogenation: You can halogenate the compound using reagents like bromine or chlorine to introduce halogen atoms onto the pyrazine rings.
Condensation Reactions: It can participate in various condensation reactions, such as Mannich reactions, to form more complex molecules.
Metalation: Metal-catalyzed reactions can be employed to introduce metal atoms or groups onto the pyrazine rings.
Cyclization: The compound can undergo intramolecular cyclization reactions to form other fused or bridged heterocycles.
Nucleophilic Substitution: Depending on the reaction conditions, nucleophilic substitution reactions can take place at various positions within the molecule.

1H-pyrazolo[3,4-b]pyrazine

A124800272-60-697%

$40.00/100mg

A4848381935196-58-998%

$88.00/1g

A2379081260664-81-095%

$49.00/1g

A1682031196152-90-594%

$204.00/250mg

A73415781411-68-997%

$4044.00/100g