Gyrase inhibitors and uses thereof
AssigneeVertex Pharmaceuticals Incorporated
InventorsPaul Charifson, David Deininger, Anne-Laure Grillot, Yusheng Liao, Steven Ronkin, Dean Stamos, Emanuele Perola, Tiansheng Wang, Arnaud LeTiran, Joseph Drumm
Life of this patent
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Abstract
The present invention relates to compounds that inhibit bacterial gyrase and/or Topo IV and pharmaceutically acceptable compositions comprising said compounds. These compounds, and compositions thereof, are useful in treating bacterial infection. Accordingly, the present invention also relates to methods for treating bacterial infections in mammals.
Claims25
A compound of formula VII:
- or a pharmaceutically acceptable salt thereof, wherein:
- V is selected from nitrogen, CH, or CF;
- R3 is hydrogen or C1-4 aliphatic, wherein:
- when R3 is Cl1-4 aliphatic, R3 is substituted with 0-3 groups independently selected from OH, R5, or OR5;
- wherein:
- R5 is C1-3 aliphatic, wherein:
- two R5 aliphatic groups may be optionally taken together with the carbon to which they are bound to form a C3-4 cycloalkyl ring;
- provided that if R3 is hydrogen, then V is not nitrogen or CH;
- R4 is a C1-3 aliphatic group;
- and
- Ring C is a 6-membered heteroaryl ring having 1-2 nitrogens, wherein:
- Ring C is substituted with 1-3 groups selected from R6;
- wherein:
- each R6 is independently selected from OR7 or halogen;
- and
- R7 is C1-4 aliphatic;
- or
- Ring C is an unsubstituted 2-pyrimidine ring.
(canceled)
13-14. (canceled)
A compound selected from the group consisting of:
22-24. (canceled)
26-27. (canceled)
29-30. (canceled)
Dependencies are inferred from the claim text.