Home Chemistry Heterocyclic Building Blocks Imidazolidines (3Ar,6As)-Tetrahydro-1H-Thieno[3,4-D]Imidazol-2(3H)-One
Ring Opening Reactions: The imidazolidinone ring can undergo ring-opening reactions with various nucleophiles, such as amines or alcohols, to form different derivatives.
Alkylation: The compound can be alkylated by reacting it with alkyl halides or other alkylating agents, leading to the introduction of alkyl groups.
Acylation: The compound can be acylated by reacting it with acyl halides or anhydrides, leading to the introduction of acyl groups.
Reduction: The ketone group in the molecule can be reduced to form the corresponding alcohol using reducing agents like sodium borohydride (NaBH4) or lithium aluminum hydride (LiAlH4).
Nucleophilic Substitution: The compound can undergo nucleophilic substitution reactions at various positions in the molecule, depending on the reagents and conditions used.
Oxidation: The compound can be oxidized, converting the thienoimidazolidinone ring into other functional groups.
Hydrolysis: Under acidic or basic conditions, the compound can undergo hydrolysis of the imidazolidinone ring to form different products.
Cyclization: Depending on the reaction conditions, it may undergo intramolecular cyclization reactions to form cyclic compounds.
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 :