Microwave Irradiation in Solvent-Free Conditions: Preparation of 2-Substituted-4(3H)-quinazolinones by Heterocyclization of 2-Aminobenzamide with Carboxylic Acids.

ChemInform ◽  
2004 ◽  
Vol 35 (28) ◽  
Author(s):  
M. Rahimizadeh ◽  
Z. Tavallai ◽  
M. Bakavoli
2005 ◽  
Vol 2005 (2) ◽  
pp. 119-120 ◽  
Author(s):  
Majid M. Heravi ◽  
Dordaneh Zargarani ◽  
Rahim Hekmat Shoar ◽  
Shahnaz Khaleghi

Amides efficiently and rapidly give carboxylic acids in high yields upon reaction with phthalic anhydride under microwave irradiation in the absence of solvent.


2015 ◽  
Vol 11 ◽  
pp. 2021-2028 ◽  
Author(s):  
Kandasamy Rajaguru ◽  
Arumugam Mariappan ◽  
Rajendran Suresh ◽  
Periasamy Manivannan ◽  
Shanmugam Muthusubramanian

The reaction of α-azidochalcones with carboxylic acids has been investigated resulting in the formation of α-amido-1,3-diketones under microwave irradiation via in situ formation of 2H-azirine intermediates. An interesting reaction is described wherein, with trifluoroacetic acid at lower temperature, it affords highly substituted 2-(trifluoromethyl)oxazoles. These flexible transformations proceed under solvent free conditions in good to excellent yields without any catalyst.


1999 ◽  
Vol 23 (9) ◽  
pp. 574-575
Author(s):  
Firouz Matloubi Moghaddam ◽  
Mohammad Ghaffarzadeh ◽  
Seyed Hossein Abdi-Oskoui

An AICl3–ZnCl2 mixture supported on silica gel is found to be an efficient medium for the Fries rearrangement of acyloxybenzene or naphthalene derivatives in solvent-free conditions under microwave irradiation.


RSC Advances ◽  
2021 ◽  
Vol 11 (45) ◽  
pp. 28061-28071
Author(s):  
Kesatebrhan Haile Asressu ◽  
Chieh-Kai Chan ◽  
Cheng-Chung Wang

Trisubstituted imidazoles are synthesized efficiently from the readily available 1,2-diketones and aldehydes using hexamethyldisilazane as a new and stable nitrogen source under TMSOTf-catalysis system, microwave heating and solvent-free conditions.


2005 ◽  
Vol 2005 (1) ◽  
pp. 27-28 ◽  
Author(s):  
Jaime Charris ◽  
Arthur Barazarte ◽  
José Domínguez ◽  
Neira Gamboa

A rapid method for the preparation of N-aryl-2-methylthio-4-oxo-1,4-dihydro quinoline-3-carbonitriles (2a–e) and N-aryl-3-methylthio-4H-1,4-benzothiazine-2-carbonitrile 1,1-dioxides (2f–o) is reported. The cyclization is accelerated by microwave irradiation under solvent free conditions in the presence of K2CO3.


ChemInform ◽  
2007 ◽  
Vol 38 (24) ◽  
Author(s):  
Julio A. Seijas ◽  
M. Pilar Vazquez-Tato ◽  
M. Raquel Carballido-Reboredo ◽  
Jose Crecente-Campo ◽  
Lucia Romar-Lopez

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