Methyl mercapturate synthesis: an efficient, convenient and simple method.
Benoît Cossec, Frédéric Cosnier, Manuella Burgart
Index: Molecules 13(10) , 2394-407, (2008)
Full Text: HTML
Abstract
A safe and simple method for methyl S-arylmercapturate synthesis is described. Thirteen such compounds, to be used afterwards in metabolism studies, have been obtained with yields ranging from 71 to 99.6%. These compounds were obtained using a sulfa-Michael addition and synthesized by adding the corresponding thiophenols to a mixture composed of methyl 2-acetamidoacrylate (MAA), potassium carbonate and a phase transfer catalyst, Aliquat 336. MAA, the initial synthon, was itself isolated in quasi quantitative yield following a fully described synthesis.
Related Compounds
Related Articles:
2005-11-25
[Biochem. Pharmacol. 70(11) , 1579-92, (2005)]
2008-12-01
[Am. J. Physiol. Renal Physiol. 295(6) , F1825-35, (2008)]
Orthogonal synthesis of indolines and isoquinolines via aryne annulation.
2008-02-06
[J. Am. Chem. Soc. 130(5) , 1558-9, (2008)]
2012-03-21
[J. Am. Chem. Soc. 134(11) , 5131-7, (2012)]
Asymmetric hydrogenation using chiral Rh complexes immobilised with a new ion-exchange strategy.
2005-04-21
[Org. Biomol. Chem. 3(8) , 1547-50, (2005)]