Please use this identifier to cite or link to this item: http://dl.merc.ac.ir/handle/Hannan/52918
Title: Expedient Base-Mediated Desulfitative Dimethylamination, Oxidation, or Etherification of 2-(Methylsulfanyl)-3,5-dihydro-4H-imidazol-4-one Scaffolds
Authors: Khan, Shahnawaz
Tyagi, Vikas
Mahar, Rohit
Bajpai, Vikas
Kumar, Brijesh
Chauhan, P M S
Keywords: Heterocycles;Aminations;Etherifications;Oxidations;Ketones;Amines;Ethers
Issue Date: 2013
Description: The dimethylamino functionality is generally introduced onto the 3,5-dihydro-4H-imidazol-4-one skeleton by treatment of a halogenated derivative with low-boiling dimethylamine at a high temperature and pressure. The corresponding aliphatic ethers are usually prepared by Williamson ether synthesis, but the available transition-metal-catalyzed methods require highly toxic reagents (such as dimethyl sulfate or methyl halides) and expensive metal catalysts, and they entail harsh reaction conditions and complex workups. A simple and efficient method is described for base-mediated¬ desulfitative dimethylamination, oxidation, or etherification at the C2-position of the 2-(methylsulfanyl)-3,5-dihydro-4H-imidazol-4-one scaffold by using potassium carbonate and aqueous N,N-dimethylformamide or an aliphatic alcohol.
URI: http://hdl.handle.net/123456789/1403
Other Identifiers: Synthesis, 2013, 45(17), 2405-2412
Appears in Collections:Medicinal and Process Chemistry

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