Synthesis and conversions of 5-(3,5-6-trichloro-1,4-benzoquinon-2-yl)-2-isopropylidenehydrazinothiazole and 2-isopropylidenazinothiazolines

Autor: Karlivan, G. A., Valter, R. É., Batse, A. É., Gulbis, Yu. V.
Zdroj: Chemistry of Heterocyclic Compounds; October 1996, Vol. 32 Issue: 10 p1227-1233, 7p
Abstrakt: When 2,5-dihydroxy-3,4,6,7-tetrachloro-2,3-dihydrobenzo[b]furan interacts in acetone with thiosemicarbazide or its 4-methyl or 4-phenyl derivative, the respective products are 5-(2,5-dihydroxy-3,4,6-trichlorophenyl)-2-(isopropylidenehydrazino)thiazole and -3-R-2-(isopropylidenazino)thiazolines, respectively. It has been shown that hydrolysis of these compounds forms 3-amino-5-(2,5-dihydroxy-3,4,6-trichlorophenyl)-2-imino(or 2-R-imino)thiazolines. These products of hydrolysis and their predecessors are oxidized to the corresponding 2-hetaryl-substituted 3,5,6-trichloro-1,4-benzoquinones.
Databáze: Supplemental Index