A Synthesis of Functionalized 2-Indolizin-3-yl-1,3-benzothiazoles from 1-(1,3-Benzothiazol-2-ylmethyl)pyridinium Iodide and Acetylenic Esters

被引：10
作者：
Yavari, Issa [1 ]
Ghafouri, Kiyana [1 ]
Naeimabadi, Maryam [1 ]
Halvagar, Mohammad Reza [2 ]
机构：
[1] Tarbiat Modares Univ, Dept Chem, POB 14115-175, Tehran, Iran
[2] Chem & Chem Engn Res Ctr Iran, Dept Inorgan Chem, POB 14335-186, Tehran, Iran
来源：
SYNLETT | 2018年 / 29卷 / 02期
关键词：
indolizinylbenzothiazoles; alkynoate esters; ylide; benzothiazolylpyrroloisoquinolines; 1,3-DIPOLAR CYCLOADDITION; BIOLOGICAL-PROPERTIES; ANTITUMOR; BENZOTHIAZOLES; DERIVATIVES; INDOLIZINES; DESIGN; YLIDES; POTENT; AGENTS;
D O I：
10.1055/s-0036-1590910
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Functionalized 2-indolizin-3-yl-1,3-benzothiazoles were obtained in moderate yields from the reaction between 1-( 1,3-benzothiazol-2-ylmethyl) pyridinium iodide and acetylenic esters in acetonitrile. When isoquinoline was used under similar conditions, dialkyl 3( 1,3-benzothiazol-2-yl) pyrrolo[2,1-alpha] isoquinoline-1,2-dicarboxylates were obtained. The structures of these products have been confirmed by X-ray diffractometry.
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收藏
页码：243 / 245
页数：3
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