化学
丙二腈
Knoevenagel冷凝
试剂
加合物
水溶液
有机化学
氨
药物化学
催化作用
作者
C. V. Asokan,E. R. Anabha,K. Nirmala,Abraham Thomas
出处
期刊:Synthesis
[Thieme Medical Publishers (Germany)]
日期:2007-01-25
卷期号:2007 (3): 428-432
被引量:15
标识
DOI:10.1055/s-2006-958964
摘要
The Knoevenagel adducts of 2-aroyl-3,3-bis(alkylsulfanyl)acrylaldehydes and malononitrile were cyclized in the presence of diisopropylamine to afford 5-aroyl-2,6-bis(methylsulfanyl)nicotinonitriles. Cyclization in the presence of aqueous ammonia gave 2-amino-5-aroyl-6-(methylsulfanyl) nicotinonitriles. A multicomponent reaction involving aroylketene dithioacetals, malononitrile and Vilsmeier reagent gave 5-aroyl-2-chloro-6-(methylsulfanyl)nicotinonitrile.
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