首页 | 本学科首页   官方微博 | 高级检索  
     


New Routes to Oxindole Derivatives
Authors:Márta?Porcs-Makkay,Balázs?Volk,Rita?Kapiller-Dezsófi,Tibor?Mezei,Gyula?Simig  author-information"  >  author-information__contact u-icon-before"  >  mailto:simig.gyula@egis.hu"   title="  simig.gyula@egis.hu"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Chemical Research Division, EGIS Pharmaceuticals Ltd., 1475 Budapest, Hungary
Abstract:Summary. A new, practical synthesis of the antirheumatic oxindole derivative, tenidap, has been elaborated. The new approach has initiated studies on the mechanism of the acylation reactions of oxindoles. Methods have been developed for the synthesis of 1-[alkoxy(or aryloxy)carbonyl]- and 1,3-di[alkoxy(or aryloxy)carbonyl]oxindoles starting from oxindoles. The route designed for tenidap has provided a facile access to several analogues, too.On another front, new reaction conditions are described, which turn Wenkertrsquos synthesis of 3-alkyloxindoles (by Raney nickel induced alkylation of oxindoles with alcohols) into a highly efficient synthetic tool. The method has been extended to the synthesis of 3-alkyloxindoles from isatins and to the preparation of 3-(ohgr-hydroxyalkyl)oxindoles from oxindoles and isatins.
Keywords:. Acylation   Alkylation   Isatins   Oxindoles   Regioselectivity.
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号