NEW CHEMISTRY OF N,N′-BIS(ARYL)-ETHANE-l,2-DIYLIDENEDIAMINES TOWARDS CARBON DISULFIDE AND PHENYL ISOTHIOCYANATE
作者:Ashraf A. Aly、Nasr K. Mohamed、Boul-Fetouh E. Mourad
DOI:10.1080/10426509908036995
日期:1999.5.1
Abstract N,N′-Bis(aryl)-ethane-1,2-diylidenediamine (1a,b) reacts with carbon disulfide to give 5-hydroxy-2-arylamino-3N-arylamino-4H-1, 3-thiazoline-2-thione (2a,b) in addition to N-aryl-thiourea derivatives 3–5. The reaction of phenyl isothiocyanate with 1a,b provides 1,2-diphenylamino-1,1,2,2-tetra-arylamino-ethane (6a,b), 1N-phenyl-3N-aryl-diazetidine-2,4-dithione (7a,b) and 1-toluidino-1,1, 2
摘要 N,N'-双(芳基)-乙烷-1,2-二亚苯基二胺(1a,b)与二硫化碳反应生成5-羟基-2-芳基氨基-3N-芳基氨基-4H-1, 3-thiazoline-2 -硫酮 (2a,b) 以及 N-芳基硫脲衍生物 3-5。异硫氰酸苯酯与 1a,b 反应生成 1,2-二苯基氨基-1,1,2,2-四芳基氨基-乙烷 (6a,b)、1N-苯基-3N-芳基-二氮杂环丁烷-2,4-二硫酮(7a,b) 和 1-toluidino-1,1, 2,2-tetra-aryllarnino-ethane (8a,b)。