474309-06-3Relevant articles and documents
A traceless solid-phase synthesis of 2-imidazolones
Cheng, Jie-Fei,Kaiho, Christopher,Chen, Mi,Arrhenius, Thomas,Nadzan, Alex
, p. 4571 - 4573 (2002)
A traceless solid-phase synthesis of 2-imidazolones has been developed. Polymer-bound glycerol resin was reacted with bromoacetaldehyde diethyl acetal to give the cyclic acetal bromide on the solid support. Amination of the resin-bound acetal bromide followed by urea formation by reaction with isocyanates afforded the resin-bound urea acetals. The aldehyde urea intermediate, which was released from the resin upon treatment with TFA, immediately cyclized to afford the desired 2-imidazolones in good yield and purity.
Efficient solid-phase synthesis of disubstituted 1,3-dihydro-imidazol-2- ones
Rossé, Gérard,Strickler, Julie,Patek, Marcel
, p. 2167 - 2168 (2007/10/03)
A bromoacetal linker was used to achieve the synthesis of ureas on a solid support. The resulting ureido acetals were treated with TFA and were converted in an intramolecular cyclization via N-acyliminium ion to disubstituted 1,3-dihydro-imidazol-2-ones.