A new synthetic process of dapagliflozin
	    		
		   		
		   			
		   		
	    	
    	 
    	10.11665/j.issn.1000-5048.20170106
   		
        
        	
        		- VernacularTitle:达格列净合成工艺的改进
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Li MA
			        		
			        		;
		        		
		        		
		        		
			        		Menghan ZHANG
			        		
			        		;
		        		
		        		
		        		
			        		Zhiwei XU
			        		
			        		;
		        		
		        		
		        		
			        		Yingai SUN
			        		
			        		;
		        		
		        		
		        		
			        		Jing ZHU
			        		
			        		;
		        		
		        		
		        		
			        		Yingbo HUANG
			        		
			        		;
		        		
		        		
		        		
			        		Dayong ZHANG
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		SGLT2 inhibitors;
			        		
			        		
			        		
				        		dapagliflozin;
			        		
			        		
			        		
				        		synthesis;
			        		
			        		
			        		
				        		process improvement;
			        		
			        		
			        		
				        		antidiabetic agents
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Journal of China Pharmaceutical University
	            		
	            		 2017;48(1):42-45
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	This paper describes a practical process for a SGLT2 inhibitor dapagliflozin. The target product was synthesized from 1-chloro-2-( 4-ethoxybenzyl)-4-iodobenzene and 2, 3, 4, 6-tetra-O-acetyl-alpha-D-glucopyranosyl bromide by iodine-magnesium exchange, and coupling and acetyl removing reactions with the total yield of 50%. This practical process highlights fewer reaction steps, less waste and mild reaction conditions.