One-pot sequential multi-component reaction: Synthesis of 3-substituted indoles

被引:8
|
作者
Borpatra, Paran J. [1 ]
Deka, Bhaskar [1 ]
Rajbongshi, Basanta K. [2 ]
Deb, Mohit L. [1 ]
Baruah, Pranjal K. [1 ]
机构
[1] Gauhati Univ, Dept Appl Sci, GUIST, Gauhati 781014, Assam, India
[2] Cotton Univ, Dept Chem, Gauhati, Assam, India
关键词
Alkylideneindolenine intermediate; 3-indolylalcohol; one-pot; sequential transformation; 3-substituted indole; IN-VITRO; CASCADE REACTIONS; DERIVATIVES; CHEMISTRY; BIS(INDOLYL)METHANES; ALDEHYDES; EFFICIENT; ROUTE; ACID;
D O I
10.1080/00397911.2018.1482352
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Here, we have developed a 3-component one-pot sequential approach to 3-substituted indoles. The main advantages of this process are step economy, reduced waste, and operational simplicity. The method involves in situ generation of 3-indolylalcohols from the reaction of indoles and aldehydes in the presence of base. Further, nucleophilic substitution of 3-indolylalcohols with various nucleophiles affords 3-substituted indole derivatives. The reaction does not requires any hazardous and expensive metal catalyst. In addition, the reaction is carried out in (1:1) ethanol-water which is considered as environmentally benign solvent. On the other hand, nonsequential 3-component reaction results in the formation of unwanted bisindolylmethanes. [GRAPHICS] .
引用
收藏
页码:2074 / 2082
页数:9
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