反応 #81578
ord-2cfee49587a7491f9b68ddf95299674a
反応方程式
benzenesulfonyl chloride
5-chloro-2-(2-hydroxyethyl)-7-[(2,4,6-trimethylphenyl)methoxy]anthra-[1,9-cd]pyrazol-6(2H)-one
5-chloro-2-(2-hydroxyethyl)-7-[(2,4, 6-trimethylphenyl)methoxy]anthra-[1,9-cd]pyrazol-6(2H)-one
5-chloro-2-(2-hydroxyethyl)-10-[(2,4,6-trimethylphenyl) methoxy]anthra-[1,9-cd]pyrazol-6(2H)-one
5-chloro-2-(2-hydroxyethyl)-10-[(2,4,6-trimethylphenyl)methoxy]anthra-[1,9-cd]pyrazol-6(2H)-one
→
反応物
benzenesulfonyl chloride
5-chloro-2-(2-hydroxyethyl)-7-[(2,4,6-trimethylphenyl)methoxy]anthra-[1,9-cd]pyrazol-6(2H)-one
5-chloro-2-(2-hydroxyethyl)-7-[(2,4, 6-trimethylphenyl)methoxy]anthra-[1,9-cd]pyrazol-6(2H)-one
5-chloro-2-(2-hydroxyethyl)-10-[(2,4,6-trimethylphenyl) methoxy]anthra-[1,9-cd]pyrazol-6(2H)-one
5-chloro-2-(2-hydroxyethyl)-10-[(2,4,6-trimethylphenyl)methoxy]anthra-[1,9-cd]pyrazol-6(2H)-one
試薬
なし
反応条件
詳細条件
See reaction.notes.procedure_details.
実験手順
Starting with benzenesulfonyl chloride and the mixture of regioisomers of 5-chloro-2-(2-hydroxyethyl)-7-[(2,4,6-trimethylphenyl)methoxy]anthra-[1,9-cd]pyrazol-6(2H)-one II and 5-chloro-2-(2-hydroxyethyl)-10-[(2,4,6-trimethylphenyl) methoxy]anthra-[1,9-cd]pyrazol-6(2H)-one III, using the procedure of example 3, the title compound was prepared.