Divergent reaction pathways for one-pot, three-component synthesis of novel 4H-pyrano[3,2-h]quinolines under ultrasound irradiation

被引:29
作者
Al-Bogami, Abdullah S. [1 ]
Saleh, Tamer S. [1 ,2 ]
Zayed, Ehab M. [1 ,2 ]
机构
[1] King Abdulaziz Univ, Fac Sci, Dept Chem, Jeddah 21589, Saudi Arabia
[2] Natl Res Ctr, Green Chem Dept, Cairo 12622, Egypt
关键词
Ultrasound irradiation; p-Toluenesulfonic acid; Pyranoquinoline derivatives; beta-Ketosulfone; Multicomponent reaction (MCR); PYRROLYL ARYL SULFONES; REVERSE-TRANSCRIPTASE; PROMOTED SYNTHESIS; MOIETY; SONOCHEMISTRY; DERIVATIVES; CYCLIZATION; ISOXAZOLES; QUINOLINE; PYRAZOLES;
D O I
10.1016/j.ultsonch.2013.03.003
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
The present paper deal with the multi-component condensation of 8-hydroxy quinoline, aromatic aldehydes, and sulfone derivatives catalyzed by p-toluenesulfonic acid for the synthesis of a series of 4H-pyrano[3,2-h]quinoline derivatives in ethanol under ultrasonic irradiations. We provide a series of quinoline derivatives containing sulfone moiety interesting for biological screening tests. The reactions were carried out under both conventional and ultrasonic irradiation conditions. In general, improvement in rates and yields were observed when reactions were carried out under sonication compared with classical silent conditions. Also, also, sonochemical reaction give different reaction pathway other than silent reaction. These remarkable effects appeared in sonicated reactions can be reasonably interpreted in terms of acoustic cavitation phenomenon. Structures of the products were established on analytical and spectral data. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:1194 / 1202
页数:9
相关论文
共 48 条
[1]   Facile Synthesis and In-Vitro Antitumor Activity of Some Pyrazolo[3,4-b]pyridines and Pyrazolo[1,5-a]pyrimidines Linked to a Thiazolo[3,2-a]benzimidazole Moiety [J].
Abdel-Aziz, Hatem A. ;
Saleh, Tamer S. ;
El-Zahabi, Heba S. A. .
ARCHIV DER PHARMAZIE, 2010, 343 (01) :24-30
[2]  
Ahmed N. S., CURRENT ORG IN PRESS
[3]  
Al-Bogami AS, 2011, ASIAN J CHEM, V23, P3045
[4]   SYNTHESIS OF 4-METHYLENE-1,3-NAPHTHOXAZINES BY THE REACTION OF IMINES WITH TRIPHOSGENE [J].
Al-Bogami, Abdullah Saad .
SYNTHETIC COMMUNICATIONS, 2011, 41 (19) :2952-2958
[5]   Cyclization of Hydrazones of 2-Acetyl-1-naphthol and 1-Acetyl-2-naphthol with Triphosgene. Synthesis of Spiro Naphthoxazine Dimers [J].
Al-Bogami, Abdullah Saad ;
Al-Majid, Abdullah Mohammed ;
Al-Saad, Mohammed Ali ;
Mousa, Ahmed Amine ;
Al-Mazroa, Sara Abdullah ;
Alkhathlan, Hamad Zaid .
MOLECULES, 2009, 14 (06) :2147-2159
[6]  
Albogami AS, 2012, ORIENT J CHEM, V28, P619
[7]   SYNTHESIS OF PYRRYL ARYL SULFONES TARGETED AT THE HIV-1 REVERSE-TRANSCRIPTASE [J].
ARTICO, M ;
SILVESTRI, R ;
STEFANCICH, G ;
MASSA, S ;
SCINTU, F ;
PAGNOZZI, E ;
MASU, D ;
PINNA, E ;
TINTI, E ;
LACOLLA, P .
ARCHIV DER PHARMAZIE, 1995, 328 (03) :223-229
[8]   Structure-based design, synthesis, and biological evaluation of navel pyrrolyl aryl sulfones: HIV-1 non-nucleoside reverse transcriptase inhibitors active at nanomolar concentrations [J].
Artico, M ;
Silvestri, R ;
Pagnozzi, E ;
Bruno, B ;
Novellino, E ;
Greco, G ;
Massa, S ;
Ettorre, A ;
Loi, AG ;
Scintu, F ;
La Colla, P .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (09) :1886-1891
[9]   2-Sulfonyl-4-chloroanilino moiety: A potent pharmacophore for the anti-human immunodeficiency virus type 1 activity of pyrrolyl aryl sulfones [J].
Artico, M ;
Silvestri, R ;
Massa, S ;
Loi, AG ;
Corrias, S ;
Piras, G ;
LaColla, P .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (02) :522-530
[10]  
Berlan J., 1996, ADV SONOCHEMISTRY, V4, P54