387381-73-9Relevant academic research and scientific papers
Conversion of N-(1-arylsulfonyl-2,2-dichloroethenyl)carboxamides into derivatives of 4,5-dimercaptooxazole
Babii,Zyabrev,Drach
, p. 1149 - 1152 (2007/10/03)
In reaction of excess thiols with α-arylsulfonyl-substituted enamides containing two chlorine atoms in β-position to the amide moiety the chlorine atoms and the arylsulfonyl group attached to the C = C bond are replaced by alkylthio or arylthio groups. The sulfur-containing enamides obtained undergo cyclization when treated with phosphorus pentachloride or thionyl chloride to furnish 4,5-dimercaptooxazoles used for preparation of the corresponding disulfonyl derivatives. The latter were also obtained by treating in succession the N-(1-arylsulfonyl-2,2-dichloroethenyl)carboxamides with sodium hydrosulfide, then with alkyl halides, and hydrogen peroxide in acetic acid.
