One pot synthesis of ethyl carboxylate and acetyl selenolo[2,3-b]quinoline derivatives and their tetra/pentacyclic systems

被引:3
|
作者
Gobouri, Adil A. [1 ]
Alshanbari, Naif A. [1 ]
Mohamed, Mosselhi A. M. [1 ,2 ]
Abdel-Hafez, Shams H. [1 ,3 ]
机构
[1] Taif Univ, Fac Sci, Dept Chem, At Taif 21974, Saudi Arabia
[2] Cairo Univ, Fac Sci, Dept Chem, Giza, Egypt
[3] Assiut Univ, Fac Sci, Dept Chem, Assiut 71516, Egypt
关键词
Selenolo[2,3-b]quinoline; pyrimido[4 ',5 ',4,5]selenolo[2,3-b]quinoline; thiazino[2 ',3 ',4,5]selenolo[2,3-b]quinoline; oxazino[2 ',3 ',4,5]selenolo[3,2-b]quinoline; pyrido[2 ',3 ',4,5]selenolo[2,3-b]quinoline; selenolo[2 ',3 ',5,6]pyrido [2 '',3 '',4,5] selenolo[2,3-b]quinoline;
D O I
10.1080/10426507.2019.1662015
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Ethylcarboxylate and acetyl selenoloquinoline derivatives were prepared in a one pot synthesis via reaction of sodium hydrogen selenide and 2-chloro-3-cyano-4-methylquinoline followed by reactions with ethyl chloroacetate and chloro acetone respectively which used as precursors to synthesize many of tetra and pentacyclic systems. A new series of pyrimido [4 ',5 ':4,5]selenolo[2,3-b]quinoline, thiazino[2',3':4,5]selenolo[2,3-b]quinoline, oxazino[2',3':4,5]selenolo[3,2-b]quinoline, pyrido[2 ',3 ':4,5]selenolo[2,3-b]quinoline, pyrido[2 ',3 ':4,5]selenolo[2,3-b]quinoline-2-substituted selenyl and selenolo[2 ',3 ':5,6]pyrido[2 '',3 '':4,5]selenolo[2,3-b]quinoline derivatives were prepared. Elemental analysis, IR, H-1 NMR, C-13 NMR and mass spectra confirmed the structures of the newly synthesized compounds. [GRAPHICS] .
引用
收藏
页码:211 / 217
页数:7
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