Home Chemistry Heterocyclic Building Blocks Pyridines 4-(Pyridin-2-Yl)Morpholine
Nucleophilic Substitution: The nitrogen atom in the morpholine ring can act as a nucleophile and undergo substitution reactions with electrophiles. For example, it can react with alkyl halides to form N-alkylated morpholines.
Acylation: The nitrogen in the morpholine ring can react with acyl chlorides or anhydrides to form amides. This is known as acylation, and the product would be a 4-(pyridin-2-yl)morpholine amide.
Alkylation: 4-(pyridin-2-yl)morpholine can undergo alkylation reactions with alkyl halides or alkyl sulfonates to introduce alkyl groups onto the nitrogen in the morpholine ring.
Oxidation: The pyridine ring can undergo oxidation reactions. For example, it can be oxidized to the corresponding pyridine N-oxide using reagents like hydrogen peroxide.
Reduction: If there are reducible functional groups present in the molecule, 4-(pyridin-2-yl)morpholine can be reduced using appropriate reducing agents.
Ring Opening: The morpholine ring can be opened under acidic or basic conditions, leading to the formation of compounds with open-chain structures.
Condensation Reactions: It can participate in condensation reactions, especially with carbonyl compounds, to form products like Mannich bases.
Heterocyclic Chemistry: The pyridine ring can participate in various heterocyclic chemistry reactions, including reactions involving its nitrogen and carbon atoms.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
click to sign in and save
2-Morpholinoisonicotinic acid hydrochloride
click to sign in and save
6-Morpholinonicotinoyl chloride hydrochloride
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :