82721-94-6Relevant articles and documents
A NEW GENERAL SYNTHESIS OF 2-(N-MONO- AND N-DI-SUBSTITUTED AMINO)THIAZOLES
Brown, Michael D.,Gillon, David W.,Meakins, G. Denis,Whitham, Gordon H.
, p. 1623 - 1626 (1985)
Although α-mercapto ketones react with cyanamides to give substituted 2-aminothiazoles the yields are satisfactory in only the simplest cases.However, a range of 2-aminothiazoles with substituents on the ring or the exo-nitrogen atom was obtained efficiently by the following one-pot procedure: a solution of an α-mercapto ketone anion was generated by treating an O-ethyl S-2-oxoethyl dithiocarbonate with piperidine at 20 deg C, a cyanamide was added, and the solution was heated for 3-6 h.
A New General Synthesis of N-Mono- and N-Di-substituted 2-Aminothiazoles
Brown, Michael D.,Gillon, David W.,Meakins, G. Denis,Whitham, Gordon H.
, p. 444 - 445 (2007/10/02)
Solutions of α-mercapto-ketone anions, generated from O-ethyl S-2-oxoethyl dithiocarbonates and piperidine, react with cyanamides to give 2-aminothiazoles with substituents on the heterocycle or the exo-nitrogen atom.