A Convenient Synthesis of 5-Aryltropolones via Novel Benzidine Type Rearrangement of 2-(2-Arylhydrazino)tropones
作者:Tetsuo Nozoe、Kahei Takase、Hiroaki Saito、Hiroshi Yamamoto、Kimiaki Imafuku
DOI:10.1246/cl.1986.1577
日期:1986.9.5
Treatment of a wide variety of 2-(2-arylhydrazino)tropones with ethanolic acid at 50–80 °C readily gave the benzidine type rearrangement products, i.e. 2-amino-5-(4-aminoaryl)tropones, which in turn were conveniently led to the corresponding 5-aryltropolones that can be utilized for synthesizing B-ring-open analogues of colchicine.
在 50–80 °C 下用乙醇酸处理各种 2-(2-芳基肼基) 托酮很容易得到联苯胺型重排产物,即 2-氨基-5-(4-氨基芳基)托酮,这反过来又很方便导致相应的 5-芳基托酚酮可用于合成秋水仙碱的 B 环开环类似物。