Study of reactions between 1,2-diaza-1,3-butadienes and N,N′-diaryl- or N,N′-dialkylthioureas
摘要:
1,2-Diaza-1,3-butadienes react with N,N'-diarylthioureas to give 2-(arylimino)-2,3-dihydrothiazole derivatives, whereas with N,N'-dialkylthioureas to afford 5,5-disubstituted 3-alkyl-2-(alkylimino)-thiazdidin-4-one derivatives. Under basic conditions, these last products surprisingly give rise to 2-thioxo-1,3,7-triazaspiro[4.4]non-8-en-4-one and 5-oxo-4-(4-substituted 5-oxo-2-thioxoimidazolidin-4yl)-2,5-dihydro-1H-pyrazole derivatives. In acidic medium, 5,5-disubstituted 3-alkyl-2-(alkylimino)-thiazolidin-4-ones are converted into 2-(alkylimino)-1-thia-3,7-diazaspiro[4.4]non-7-en-4-ones. X-Ray crystal structures of two products were determined. (C) 1999 Elsevier Science Ltd. All rights reserved.
Catalyst free, regioselective one-pot three-component synthesis of thiazol-2-imine derivatives in ionic liquid
作者:G. Santosh Kumar、S. Pushpa Ragini、H.M. Meshram
DOI:10.1016/j.tetlet.2013.08.056
日期:2013.11
A one-potthree-component approach for the synthesis of thiazol-2-imines has been described by the reaction of amine, phenyl isothiocyanate and β-nitroacrylate in [Hbim]BF4 ionicliquid. The method is applicable for aromatic, benzylic, aliphatic and cyclic amines. Reusable reaction media, regioselectivity, mild reaction condition, catalyst free and high yield of products are the salient features of