Efficient synthesis of 3-(bromomethyl)-5-methylpyridine hydrobromide

2015 ◽  
Vol 21 (4) ◽  
pp. 203-205
Author(s):  
Jianyu Guo ◽  
Yan Lu ◽  
Jin Wang

Abstract5-Methyl-3-(bromomethyl)pyridine is the key intermediate in the synthesis of rupatadine. In this article, a new preparation of 5-methyl-3-(bromomethyl)pyridine hydrobromide is reported, which used 5-methylnicotinic acid as the starting material, with a 65.9% overall yield. This method has the merits of being simple, efficient and environmentally friendly.

RSC Advances ◽  
2014 ◽  
Vol 4 (68) ◽  
pp. 36350-36356 ◽  
Author(s):  
Cédric Epoune Lingome ◽  
Gwladys Pourceau ◽  
Virginie Gobert-Deveaux ◽  
Anne Wadouachi

A mecanosynthesis of glycosylamines under solventless conditions was established. This environmentally friendly approach optimized with l-rhamnose, was investigated using a variety of amines and other carbohydrates.


Author(s):  
Zhongqing Wang ◽  
Zihong Zhou ◽  
Jingping Kou ◽  
Shuming Wu ◽  
Yongbo Xu ◽  
...  

2018 ◽  
Vol 16 (48) ◽  
pp. 9472-9476 ◽  
Author(s):  
Fei Hou ◽  
Xi-Cun Wang ◽  
Zheng-Jun Quan

An environmentally friendly oxone (20 mol%) catalyzed esterification of carboxylic acids with alcohols has been developed, providing an attractive alternative to the construction of valuable carbonyl esters.


1992 ◽  
Vol 33 (23) ◽  
pp. 3311-3314 ◽  
Author(s):  
André J. Laurent ◽  
Stanislaw Leniak

2015 ◽  
Vol 12 (7) ◽  
pp. 478-481 ◽  
Author(s):  
Raoni S.B. Goncalves ◽  
Emerson T. da Silva ◽  
Marcus Vinicius N. de Souza

2015 ◽  
Vol 39 (4) ◽  
pp. 2657-2668 ◽  
Author(s):  
Tushar R. Sutariya ◽  
Balvantsingh M. Labana ◽  
Narsidas J. Parmar ◽  
Rajni Kant ◽  
Vivek K. Gupta ◽  
...  

Triethylammonium acetate (TEAA) as a new, recyclable and environmentally friendly reaction medium for the intramolecular[3+2] cycloaddition reaction.


2019 ◽  
Vol 31 (3) ◽  
pp. 723-726 ◽  
Author(s):  
Rajesh Kumar Rapolu ◽  
V.V.N.K.V. Prasada Raju ◽  
Murthy Chavali ◽  
Naveen Mulakayala

Eco-friendly synthesis of pimavanserin was developed from the key starting material 4-isobutoxy benzylamine in three different routes using water as solvent. These reactions provide an advantage of easy workup, good yields of products and uses water as the solvent. No column purification was required for the isolation of the product.


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