US2012004408A1PendingUtilityA1

Use of Rosuvastatin Lactols as Medicaments

Assignee: LINDSAY DEREKPriority: Mar 10, 2009Filed: Mar 10, 2010Published: Jan 5, 2012
Est. expiryMar 10, 2029(~2.6 yrs left)· nominal 20-yr term from priority
A61P 3/10A61P 9/10A61P 43/00A61P 35/00A61P 9/00A61P 9/12A61P 3/06A61P 25/28A61P 29/00A61P 3/00A61P 25/00A61P 27/12C07D 405/14A61K 31/505C07D 405/06A61K 31/506
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Claims

Abstract

This invention relates to the discovery of novel rosuvastatin analogues. More specifically, the invention relates to novel rosuvastatin analogues which have utility in treating conditions treatable by the inhibition of HMG-CoA reductase.

Claims

exact text as granted — not AI-modified
1 . A compound of Formula I and pharmaceutically acceptable salts and solvates thereof: 
       
         
           
           
               
               
           
         
         for use in treating a condition treatable by the inhibition of the enzyme 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reductase), wherein condition treatable by the inhibition of HMG-CoA reductase is selected from the group consisting of: hypercholesterolemia, atherosclerosis, hyperlipidemia, cardiovascular disease, coronary heart disease, myocardial infarction, stroke, peripheral artery disease, inflammation, dementia, cancer, nuclear cataracts, diabetes and hypertension, further wherein: 
         R 1  and R 4  are independently selected from the group consisting of: hydrogen, halo, C 1-6  alkyl, C 2-6  alkenyl, C 3-6  cycloalkyl, aryl, C 1-4  alkyl aryl, heterocyclyl, and C 1-4  alkyl heteroaryl; 
         R 2  is —S(O) 2 R 9  wherein R 9  is C 1-6  alkyl, C 3-6  cycloalkyl, C 1-6  alkyl aryl or aryl; 
         R 3  is hydrogen, C 1-6  alkyl, C 2-6  alkenyl, C 3-6  cycloalkyl or aryl; 
         R 5  and R 6  are independently selected from the group consisting of: hydrogen, C 1-6  alkyl, C 1-6  haloalkyl, C 2-6  alkenyl, C 3-6  cycloalkyl, aryl, C 1-6  alkyl aryl, C 1-6  alkanoyl aryl, heteroaryl, C 1-6  alkanoyl heteroaryl and C 1-6  alkyl heteroaryl; provided always that both R 5  and R 6  are not hydrogen; 
         R 7  and R 8  are independently selected from the group consisting of: H, C 1-4  alkyl and halo; 
         X is —(CR a R b ) m (CR a ═CR b ) n (CR a R b ) o  where R a  and R b  are independently selected from the group consisting of: H, methyl, ethyl and halo and m, n, and o are independently 0, 1, 2, or 3 provided that m+n+o is not more than 3; and wherein 
         each of the above groups R 1  to R 9  may, where chemically possible, be independently optionally substituted by from 1 to 5 groups chosen independently at each occurrence from the groups comprising: halo, C 1-3  alkyl, halo C 1-3  alkyl, C 1-3  alkoxy, C 1-3  haloalkoxy, hydroxy, and cyano. 
       
     
     
         2 . A compound of  claim 1 , wherein R 1  is C 1-6  alkyl. 
     
     
         3 . A compound of  claim 1 , wherein R 2 —S(O) 2 R 9  wherein R 9  is C 1-6  alkyl. 
     
     
         4 . A compound of  claim 1 , wherein R 3  is hydrogen or C 1-6  alkyl. 
     
     
         5 . A compound of  claim 1 , wherein R 4  is optionally substituted aryl. 
     
     
         6 . A compound of  claim 1 , wherein R 1  is i-propyl, R 2  is —S(O) 2 Me, R 3  is methyl and R 4  4-fluorophenyl. 
     
     
         7 . A compound of  claim 1 , wherein R 5  is selected from the group consisting of: hydrogen, C 1-6  alkyl, aryl, C 1-6  alkyl aryl, C 1-6  alkanoyl aryl, heteroaryl, C 1-6  alkanoyl heteroaryl and C 1-6  alkyl heteroaryl. 
     
     
         8 . A compound of  claim 7 , wherein R 5  is hydrogen. 
     
     
         9 . A compound of  claim 7 , wherein R 5  is selected from the group consisting of: —C 1  alkyl-Ph, —C 2  alkyl-Ph, —C 3  alkyl-Ph, and —C 4  alkyl-Ph. 
     
     
         10 . A compound of  claim 9 , wherein R 5  is benzyl. 
     
     
         11 . A compound of  claim 7 , wherein R 5  is C 1-6 alkanoyl pyridine. 
     
     
         12 . A compound of  claim 11 , wherein R 5  is 3-methanoyl pyridine. 
     
     
         13 . A compound of  claim 1 , wherein R 6  is selected from the group consisting of: hydrogen, C 1-6  alkyl, C 1-6  haloalkyl, C 2-6  alkenyl, C 3-6  cycloalkyl, aryl, C 1-6  alkyl aryl, heteroaryl and C 1-6  alkyl heteroaryl. 
     
     
         14 . A compound of  claim 13 , wherein R 6  is selected from the group consisting of: C 1-6  alkyl, C 1-6  haloalkyl and C 2-6  alkenyl. 
     
     
         15 . A compound of  claim 14  wherein R 6  is selected from the group consisting of: methyl, ethyl, propyl, butyl, chloromethyl, chloroethyl, chloropropyl, chlorobutyl and propylene. 
     
     
         16 . A compound of  claim 13 , wherein R 6  is optionally substituted aryl. 
     
     
         17 . A compound of  claim 16 , wherein R 6  is selected from the group consisting of: C 1-6  alkoxy substituted phenyl and halo substituted phenyl. 
     
     
         18 . A compound of  claim 16 , wherein R 6  is selected from the group consisting of: 2,4,6-trifluorophenyl and 2,4-dimethoxyphenyl. 
     
     
         19 . A compound of  claim 1 , wherein R 5  is hydrogen and R 6  is an optionally substituted aromatic group. 
     
     
         20 . A compound of  claim 1 , wherein R 5  is an optionally substituted benzyl and R 6  is an optionally substituted C 1-6 alkyl, an optionally substituted C 2-6  alkenyl or a C 1-6  haloalkyl. 
     
     
         21 . A compound of  claim 1 , wherein R 5  is a C 1-6  alkanoyl heteroaryl and R 6  is an optionally substituted C 1-6 alkyl. 
     
     
         22 . A compound of  claim 1 , wherein R 7  is H and R 8  is H. 
     
     
         23 . A compound of  claim 1 , wherein R a  is H, R b  is H and m=0, n=1 and o=0. 
     
     
         24 . A compound of  claim 1  which has a structure selected from: 
       
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
       
     
     
         25 - 27 . (canceled)

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