First Gewald reaction ignited by sodium polysulfide: greener ultrasound-promoted synthesis of substituted 2-aminothiophenes in the absence of catalyst

2013 ◽  
Vol 34 (5) ◽  
pp. 458-463 ◽  
Author(s):  
Chengyuan Liang ◽  
Dong Lei ◽  
Xiuzhen Wang ◽  
Qingqing Zhang ◽  
Qizheng Yao
2008 ◽  
Vol 73 (7) ◽  
pp. 683-690 ◽  
Author(s):  
Dipti Dodiya ◽  
Amit Trivedi ◽  
Samir Jarsania ◽  
Shailesh Vaghasia ◽  
Viresh Shah

The synthesis of substituted pyrazolo[3',4':4,5]thieno[2,3-d]pyrimidin-8-ones (IIIa-j) from 5-amino-3-methyl-1H-thieno[3,2-c]pyrazole-6-carbonitrile (II) is described. The key compound II was synthesized from (5-methyl- -2,4-dihydro-3H-pyrazol-3-ylidene)malononitrile I via the Gewald reaction. The synthesis of the title compounds IIIa-j was accomplished by condensation of II with different aromatic aldehydes. The newly synthesized heterocyles were characterized by elemental analysis, IR, 1H-NMR, 13C-NMR and mass spectroscopic investigation. All the newly synthesized compounds were evaluated for antimicrobial activity against a variety of bacterial strains. .


Synthesis ◽  
2004 ◽  
pp. 3055-3059 ◽  
Author(s):  
Guichun Yang ◽  
Haiqing Zhang ◽  
Jianian Chen ◽  
Zuxing Chen

2008 ◽  
Vol 350 (17) ◽  
pp. 2740-2746 ◽  
Author(s):  
Marta Feroci ◽  
Isabella Chiarotto ◽  
Leucio Rossi ◽  
Achille Inesi

2017 ◽  
Vol 58 (14) ◽  
pp. 1408-1412 ◽  
Author(s):  
M. Saeed Abaee ◽  
Atefeh Hadizadeh ◽  
Mohammad M. Mojtahedi ◽  
Mohammad R. Halvagar

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