Amide Formation in One Pot from Carboxylic Acids and Amines via Carboxyl and Sulfinyl Mixed Anhydrides

2013 ◽  
Vol 15 (10) ◽  
pp. 2550-2553 ◽  
Author(s):  
Bartosz K. Zambroń ◽  
Srinivas R. Dubbaka ◽  
Dean Marković ◽  
Elena Moreno-Clavijo ◽  
Pierre Vogel
ChemInform ◽  
2013 ◽  
Vol 44 (37) ◽  
pp. no-no
Author(s):  
Bartosz K. Zambron ◽  
Srinivas R. Dubbaka ◽  
Dean Markovic ◽  
Elena Moreno-Clavijo ◽  
Pierre Vogel

2018 ◽  
Vol 21 (4) ◽  
pp. 298-301 ◽  
Author(s):  
Ghasem Marandi

Aim and Objective: The reaction of cyclohexylisocyanide and 2-aminopyridine-3- carboxylic acid in the presence of benzaldehyde derivatives in ethanol led to 3-(cyclohexylamino)-2- arylimidazo[1,2-a]pyridine-8-carboxylic acids in high yields. In a three component condensation reaction, isocyanide reacts with 2-aminopyridine-3-carboxylic acid and aromatic aldehydes without any prior activation. Material and Methods: The synthesized products have stable structures which have been characterized by IR, 1H, 13C and Mass spectroscopy as well as CHN-O analysis. Results: In continuation of our attempts to develop simple one-pot routes for the synthesis of 3- (cyclohexylamino)-2-arylimidazo[1,2-a]pyridine-8-carboxylic acids, aromatic aldehydes with divers substituted show a high performance. Conclusion: In conclusion, this study introduces the art of combinatorial chemistry using a simple one-pot procedure for the synthesis of new materials which are interesting compounds in medicinal and biological sciences.


1976 ◽  
Vol 7 (52) ◽  
pp. no-no
Author(s):  
A. G. JACKSON ◽  
G. W. KENNER ◽  
G. A. MOORE ◽  
R. RAMAGE ◽  
W. D. THORPE

2005 ◽  
Vol 46 (35) ◽  
pp. 5945-5947 ◽  
Author(s):  
Rogério da C. Rodrigues ◽  
Igor M.A. Barros ◽  
Edson L.S. Lima

2014 ◽  
Vol 16 (2) ◽  
pp. 604-607 ◽  
Author(s):  
Jianfei Bai ◽  
Bartosz K. Zambroń ◽  
Pierre Vogel
Keyword(s):  

ChemInform ◽  
2016 ◽  
Vol 47 (33) ◽  
Author(s):  
Peter Abranyi-Balogh ◽  
Tamas Foeldesi ◽  
Alajos Gruen ◽  
Balazs Volk ◽  
Gyoergy Keglevich ◽  
...  
Keyword(s):  

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