RING CLOSURE REACTIONS WITH NITRILES .3. FORMATION OF 2-AMINO- AND 2-OXO-3-HYDROXYINDOLES FROM REACTION OF 2'-AROYLACYLANILIDES WITH CYANIDE

被引：7

作者：

BELL, SC

WEI, PHL

机构：

[1] Research Division, Wyeth Laboratories, Inc, Radnor, Pennsylvania

来源：

JOURNAL OF HETEROCYCLIC CHEMISTRY | 1969年 / 6卷 / 05期

关键词：

D O I：

10.1002/jhet.5570060501

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Treatment of 2′‐aroylhaloacylanilides with potassium cyanide produced quinazolines, carbostyrils, and 3‐hydroxyindoles. From the reaction of 2′‐aroyl‐2,2‐dichloroacetanilides with cyanide, good yields of 2‐amino‐3‐hydroxyindoles were obtained and their reactions were studied. Copyright © 1969 Journal of Heterocyclic Chemistry

引用

页码：599 / &

共 9 条

[1] RING CLOSURE REACTIONS WITH NITRILES .2. FORMATION OF PYRROLO[1,2-A]QUINAZOLINES AND THIAZOLO[3,2-A]QUINAZOLINES [J].