Process improvement on the synthesis of atomoxetine
	    		
		   		
		   			
		   		
	    	
    	 
    	10.11665/j.issn.1000-5048.20190404
   		
        
        	
        		- VernacularTitle:托莫西汀合成工艺改进
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Qiuyue ZHANG
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Qidong YOU
			        		
			        		;
		        		
		        		
		        		
			        		Jinpeng YANG
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. 中国药科大学江苏省药物设计与优化重点实验室
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		atomoxetine;
			        		
			        		
			        		
				        		process improvement;
			        		
			        		
			        		
				        		asymmetric reduction;
			        		
			        		
			        		
				        		synthesis
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Journal of China Pharmaceutical University
	            		
	            		 2019;50(4):405-409
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Atomoxetine is a highly selective norepinephrine reuptake inhibitor. Based on the analysis of the literature methods, the synthesis process of atomoxetine was improved. Using 3-chloropropiophenone-1 as the raw material, optically pure target product was obtained by asymmetric reduction, Mitsunobu reaction and condensation reaction in three steps, with a total yield of 26%. The third-step methylation sealing operation was changed to the reaction under normal pressure, which increased the feasibility of industrialization. The improved process operation was simplified and the reaction conditions were mild, which would provide a new method for the preparation of atomoxetine.