Neat reaction microwave technology for the synthesis of N-substituted-1,4-dihydropyridines

2004 ◽  
Vol 82 (3) ◽  
pp. 427-429 ◽  
Author(s):  
Mazaahir Kidwai ◽  
Richa Mohan

Hantzsch synthesis of N-substituted-1,4-dihydropyridines (1,4-DHP) was carried out using an environmentally benign procedure. Neat reactants were subjected to microwave irradiation (MWI) to give the required products in excellent yield. Appreciable results were not obtained when conventional synthesis using neat reactants was carried out. The good yield and rate enhancement observed in the case of microwave irradiation is attributed to the uniform heating effect of microwaves.Key words: 1,4-dihydropyridines (1,4-DHP), microwave irradiation (MWI), neat reaction, solid support.

2019 ◽  
Vol 4 (2) ◽  
pp. 109-112
Author(s):  
Mujahed Shaikh ◽  
Ashvini Sonone ◽  
Mazahar Farooqui ◽  
Ayesha Durrani

A green and environmentally benign protocol is developed for the synthesis of Schiff bases of sulphur containing compound by irradiating thiazole and pyrazole aldehyde in glycerol under microwave irradiation at 70 ºC with trimethylsilyl chloride (TMSCl) as a catalyst. The method has advantages such as excellent yield, use of green solvent, easy work-up and most important the reaction completed within 2.5 min by using TMSCl catalyst. The TMSCl is an acidic catalyst, which enhances the yield of product, reaction time (with microwave, with reflux at 75 ºC and with stirring at room temperature) which can be easily removed from reaction mask.


2015 ◽  
Vol 17 (5) ◽  
pp. 3157-3163 ◽  
Author(s):  
Andrea Ojeda-Porras ◽  
Alejandra Hernández-Santana ◽  
Diego Gamba-Sánchez

A highly improved methodology for the direct amidation of carboxylic acids with amines using silica gel as a solid support and catalyst is described. Several examples using aliphatic, aromatic, unsaturated and fatty acids combined with primary and secondary amines are shown.


2016 ◽  
Vol 147 (9) ◽  
pp. 1605-1614 ◽  
Author(s):  
Dawei Zhang ◽  
Xiaodong Chen ◽  
Xue Guo ◽  
Yumin Zhang ◽  
Yaya Hou ◽  
...  

2010 ◽  
Vol 75 (3) ◽  
pp. 275-287 ◽  
Author(s):  
Mithlesh ◽  
Pawan K. Pareek ◽  
Hemraj Chippa ◽  
Ravikant ◽  
Krishan G. Ojha

2,3,5,6-Tetrasubstituted-4-aryl-1-(6-ethoxybenzothiazol-2-yl)-1,4-dihydropyridines were synthesized by the reaction of 2-amino-6-ethoxybenzothiazole, an aromatic aldehyde and an active methylene compound in methanol by conventional or microwave irradiation method (solvent-free or with solid support). All compounds were tested for antibacterial and antifungal activities and the results were compared with standard drugs. Their acaricidal and antifeedant activities were also tested.


2002 ◽  
Vol 2002 (6) ◽  
pp. 301-302 ◽  
Author(s):  
Ramesh Patnam ◽  
Fang-Rong Chang ◽  
Reen-Yen Kuo ◽  
Wen-Bin Pan ◽  
Yang-Chang Wu

Microwave irradiation of alcohols with acetic anhydride in the presence of a catalytic amount of NaOH for a few minutes yielded the corresponding acetylated products in excellent yield.


ChemInform ◽  
2010 ◽  
Vol 28 (48) ◽  
pp. no-no
Author(s):  
J. SINGH ◽  
M. SHARMA ◽  
G. L. KAD ◽  
B. R. CHHABRA

2011 ◽  
Vol 8 (2) ◽  
pp. 863-869 ◽  
Author(s):  
Tapas K. Mandal ◽  
Rammohan Pal ◽  
Rina Mondal ◽  
Asok K. Mallik

Different aromatic aldehydes and cinnamaldehyde undergo cross-aldol condensation with chroman-4-ones and1-thiochroman-4-ones in the presence of amberlyst-15 under microwave irradiation in solvent free condition to afford rapidly the correspondingE-3-arylidene andE-3-cinnamylidene derivatives, respectively, in high yield. This process is simple, efficient and environmentally benign.


Tetrahedron ◽  
2001 ◽  
Vol 57 (18) ◽  
pp. 3915-3920 ◽  
Author(s):  
Alexander Stadler ◽  
C.Oliver Kappe

2001 ◽  
Vol 31 (5) ◽  
pp. 711-717 ◽  
Author(s):  
Satya Paul ◽  
Rajive Gupta ◽  
André Loupy ◽  
Babita Rani ◽  
Anshu Dandia

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