US2009326215A1PendingUtilityA1

Glucopyranosyl-substituted phenyl derivatives, medicaments containing such compounds, their use and process for their manufacture

Assignee: BOEHRINGER INGELHEIM INTPriority: Mar 16, 2004Filed: Aug 21, 2009Published: Dec 31, 2009
Est. expiryMar 16, 2024(expired)· nominal 20-yr term from priority
A61P 7/10A61P 3/08A61P 5/50A61P 9/04A61P 5/14A61P 9/12A61P 3/04A61P 39/02A61P 9/10A61P 3/06A61P 43/00A61P 7/00A61P 9/00A61P 25/00A61P 3/00A61P 3/10A61P 1/18A61P 1/04A61P 19/06A61P 13/12C07H 15/20C07D 309/10C07H 15/04A61K 9/2018C07H 23/00A61K 9/02A61K 9/4866A61K 9/0019C07H 15/26
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Claims

Abstract

Glucopyranosyl-substituted benzene derivatives of general formula I where the groups R 1 to R 6 as well as R 7a , R 7b , R 7c are defined herein and the tautomers, the stereoisomers thereof, the mixtures thereof and the salts thereof. The compounds according to the invention are suitable for the treatment of metabolic disorders.

Claims

exact text as granted — not AI-modified
1 .- 22 . (canceled) 
   
   
       23 . Process for preparing compounds of general formula II 
     
       
         
         
             
             
         
       
       wherein 
       R′ denotes H, C 1-4 -alkyl, (C 1-18 -alkyl)carbonyl, (C 1-18 -alkyl)oxycarbonyl, arylcarbonyl and aryl-(C 1-3 -alkyl)-carbonyl, wherein the alkyl or aryl groups may be mono- or polysubstituted by halogen; 
       R 8a , R 8b , R 8c , R 8d  independently of one another have one of the meanings given for the groups R 6 , R 7a , R 7b , R 7c , denote a benzyl group or a R a R b R c Si group or a ketal or acetal group, while in each case two adjacent groups R 8a , R 8b , R 8c , R 8d  may form a cyclic ketal or acetal group or a 1,2-di(C 1-3 -alkoxy)-1,2-di(C 1-3 -alkyl)-ethylene bridge, while the above-mentioned ethylene bridge forms, together with two oxygen atoms and the two associated carbon atoms of the pyranose ring, a substituted dioxane ring, and alkyl, aryl and/or benzyl groups may be mono- or polysubstituted by halogen or C 1-3 -alkoxy and benzyl groups may also be substituted by a di-(C 1-3 -alkyl)amino group; and 
       R a , R b , R c  independently of one another denote C 1-4 -alkyl, aryl or aryl-C 1-3 -alkyl, wherein the aryl or alkyl groups may be mono- or polysubstituted by halogen; 
       while by the aryl groups mentioned in the definition of the above groups are meant phenyl or naphthyl groups, preferably phenyl groups; 
       and R 1  to R 5  and R 6 , R 7a , R 7b , R 7c  have the meanings given in claims  1 , 
       wherein an organometallic compound (V) which may be obtained by halogen-metal exchange or by the insertion of a metal in the carbon-halogen bond of a halogen-benzylbenzene compound of general formula IV 
     
     
       
         
         
             
             
         
       
       wherein Hal denotes Cl, Br and I and R 1  to R 5  are as hereinbefore defined, and optionally subsequent transmetallation, is added to a gluconolactone of general formula VI 
     
     
       
         
         
             
             
         
       
       wherein R 8a , R 8b , R 8c , R 8d  are as hereinbefore defined, and 
       then reacting the adduct obtained with water or an alcohol R′—OH, where R′ denotes optionally substituted C 1-4 -alkyl, in the presence of an acid and optionally the product obtained in the reaction with water wherein R′ denotes H is converted in a subsequent reaction with an acylating agent into the product of formula II wherein R′ denotes (C 1-18 -alkyl)carbonyl, (C 1-18 -alkyl)oxycarbonyl, arylcarbonyl or aryl-(C 1-3 -alkyl)-carbonyl, which may be substituted as specified. 
     
   
   
       24 . Process according to  claim 23 , wherein the organometallic compound (V) is a lithium or magnesium compound. 
   
   
       25 . (canceled) 
   
   
       26 . Compound of general formula IV 
     
       
         
         
             
             
         
       
       wherein Hal denotes chlorine, bromine or iodine and the groups R 1 , R 2 , R 3 , R 4  and R 5  are defined as in claim  1 . 
     
   
   
       27 . Compound of formula IV according to  claim 26 , characterised by the formula 
     
       
         
         
             
             
         
       
       wherein Hal denotes chlorine, bromine or iodine and the groups R 1 , R 2 , R 4  and R 5  are defined according to claim  1  and the group R 3  is selected from the group B according to  claim 26 . 
     
   
   
       28 . Compound of general formula II 
     
       
         
         
             
             
         
       
       wherein 
       R′ denotes H, C 1-4 -alkyl, (C 1-18 -alkyl)carbonyl, (C 1-18 -alkyl)oxycarbonyl, arylcarbonyl and aryl-(C 1-3 -alkyl)-carbonyl, wherein the alkyl or aryl groups may be mono- or polysubstituted by halogen; 
       R 8a , R 8b , R 8c , R 8d  independently of one another have one of the meanings given for the groups R 6 , R 7a , R 7b , R 7c , or denote a benzyl group or a R a R b R c Si group or a ketal or acetal group, while in each case two adjacent groups R 8a , R 8b , R 8c , R 8d  may form a cyclic ketal or acetal group or a 1,2-di(C 1-3 -alkoxy)-1,2-di(C 1-3 -alkyl)-ethylene bridge, while the above-mentioned ethylene bridge forms, together with two oxygen atoms and the two associated carbon atoms of the pyranose ring, a substituted dioxane ring, and alkyl, aryl and/or benzyl groups may be mono- or polysubstituted by halogen or C 1-3 -alkoxy and benzyl groups may also be substituted by a di-(C 1-3 -alkyl)amino group; and 
       R a , R b , R c  independently of one another denote C 1-4 -alkyl, aryl or aryl-C 1-3 -alkyl, while the alkyl or aryl groups may be mono- or polysubstituted by halogen; 
       while by the aryl groups mentioned in the definition of the above groups are meant phenyl or naphthyl groups, preferably phenyl groups; 
     
     and R 1  to R 5  are defined as in one or more of claim  1 .

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