78554-09-3Relevant academic research and scientific papers
Reactions of 4-chloro-5H-1,2,3-dithiazol-5-thione with primary and secondary alkylamines : Novel method for preparing N-alkyl- and N,N-dialkylcyanothioformamides
Lee, Hyi-Seung,Kim, Kyongtae
, p. 3709 - 3712 (1996)
Treatment of 4-chloro-5H-1,2,3-dithiazol-5-thione with primary and secondary alkylamines in CH2Cl2 at room temperature afforded N-alkyl- and N,N-dialkylcyanothioformamides, respectively. Copyright
Reactions of Cyanodithioformates with Primary Amines
Kibbel, H. U.,Kuecken, M.,Peters, E.,Weber, H.
, p. 41 - 48 (2007/10/02)
N-alkyldithiooxamides 3 and N,N-dialkyldithiooxamides 4 were synthesized in good yields by reaction of cyanodithioformates 1 with primary aliphatic amines.N-alkylcyanodithioformamides 2, intermediates in these reactions were obtained in very low yields only.The reaction of 1 and diaminoethane or 1,3-diaminopropane afforded imidazolidine-2-thione 5a respectively perhydropyrimidine-2-thione 5b.The reaction of 1 with 1-chloro-2-aminoethane did gave 2-thiocarbamoylthiazoline 7.
