101-99-5 Transformation of a spirobarbituric acid via aminobarbituric acid-hydantoin rearrangement

A successful application of the aminobarbituric acid-hydantoin rearrangement to produce a bicyclic carbamoylhydantoin from an intermediate spirobarbituric acid is reported. 7a-Phenylcarbamoyl-tetrahydro-1H-pyrrolo[1,2- c]imidazole-1,3(2H)-dione (8) was obtained in a one-pot multistep reaction of 1-acetyl-2,2-bis(ethoxycarbonyl)pyrrolidine (5) and phenylurea in the presence of sodium ethoxide. Under less severe conditions, 5 and phenylurea were reacted to afford 1-acetyl-7-phenyl-triaza[4,5]decane-6,8,10-trione (6). The structural elucidation of the bicyclic hydantoin 8 and the spirobarbituric acid 6 was based on relevant nmr signals in accordance with those of reference compounds, i.e. monocyclic hydantoins 4a,b and acetamidobarbituric acids 2a-c. The latter compounds were newly prepared from diethyl acetamidomalonates 1 and phenylurea. https://www.lookchem.com/CASDataBase_101-99-5.htm

评论

此博客中的热门博文

100-48-1 In situ immobilized palladium nanoparticles on surface of poly-methyldopa coated-magnetic nanoparticles (Fe3O4@PMDA/Pd): A magnetically recyclable nanocatalyst for cyanation of aryl halides with K4[Fe(CN)6]

767-58-8 The Photochemistry of Conformationally Rigid Benzylic Esters: 2,2-Dimethyl-1-indanyl Acetates and Pivalates

75-09-2 Catalytic dechlorination of carbon tetrachloride in liquid phase with methanol as H-donor over AG/C catalyst