Home Chemistry Heterocyclic Building Blocks Pyrimidines 2-Methoxypyrimidin-4-Amine
Nucleophilic Substitution Reactions: The amino group can act as a nucleophile in reactions with electrophiles. For example, it can react with alkyl halides to form N-alkylated derivatives.
Acylation Reactions: The amino group can react with acyl chlorides or acid anhydrides to form amides. This is known as acylation.
Nucleophilic Aromatic Substitution: The amino group in the pyrimidine ring can participate in nucleophilic aromatic substitution reactions under certain conditions.
Reductive Amination: The amino group can undergo reductive amination reactions with carbonyl compounds (aldehydes or ketones) in the presence of a reducing agent to form secondaryamines.
Oxidation Reactions: Depending on the conditions, the amino group may be oxidized to form various products.
N-Oxidation: The amino group can be oxidized to form N-oxides under certain oxidative conditions.
Diazoes Coupling: The amino group can participate in diazo coupling reactions with diazonium salts.
Substitution at the Methoxy Group: The methoxy group at the 2-position may undergo substitution reactions, particularly if there are electrophiles present.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :