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US 2007/0167471 A1Published application
Substituted quinazoline compounds useful as p38 kinase inhibitors
AssigneeRoche Palo Alto LLC
InventorsJames Dunn, David Goldstein, Christoph Stahl, Teresa Trejo-Martin
Life of this patent
Estimating the term…
Abstract
Compounds having the formula (I), are useful as p38 kinase inhibitors, wherein R4 and R5 are hydrogen, halogen, cyano, haloalkyl, or haloalkoxy, but are not both hydrogen; R6 and R7 are optional substituents, and Q is a non-aromatic moiety as defined in the specification.
Claims16
1-17. (canceled)
A method for treating a p38-mediated disorder in a patient comprising administering to the patient in need of such treatment, an effective amount of a compound having the formula (II):
- or an isomer, prodrug, or pharmaceutically-acceptable salt thereof, wherein:
- Qa is selected from alkyl, substituted alkyl, heteroalkyl, or an optionally-substituted cycloalkyl or heterocyclic ring, provided that Q is not arylalkyl or heteroarylalkyl;
- Y is —O—, —S—, or —NR′—, wherein R′ is hydrogen, lower alkyl, or lower alkyl substituted with OH;
- R is alkyl, substituted alkyl, or optionally-substituted aryl, heteroaryl, cycloalkyl, or heterocyclyl;
- R6 is attached to any available carbon atom of the quinazoline ring and at each occurrence is independently selected from alkyl, substituted alkyl, halogen, cyano, nitro, hydroxy, alkoxy, haloalkoxy, cycloalkyl, substituted cycloalkyl, heterocyclyl, substituted heterocyclyl, aryl, substituted aryl, heteroaryl, and substituted heteroaryl;
- and
- m is 0, 1, 2or 3.
4 more elements
20-21. (canceled)
23-24. (canceled)
Dependencies are inferred from the claim text.