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US 2009/0264459 A1Published application
Organic Compounds
OwnerStephen Paul Collingwood, Robin Alec Fairhurst +1inventors
InventorsStephen Paul Collingwood, Robin Alec Fairhurst, Neil John Press
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Abstract
Compounds of formula (I) in free or a pharmaceutically acceptable salt form, wherein X1, L and Q have the meanings as indicated in the specification, are useful for treating obstructive or inflammatory airways diseases. Pharmaceutical compositions that contain the compounds and processes for preparing the compounds are also described.
Claims12
A compound of the formula (I):
- where Q is
- where X3 is
- wherein
- X1 and X2 are independently selected from S, CH2CH2, CH:CH2 or CH20;
- Ar1 is a phenyl, pyridyl, diazinyl or triazinyl group optionally substituted by one or two moieties selected from methyl, ethyl, fluorine, chlorine, bromine, cyano, methoxy, ethoxy, methoxymethyl, trifluoromethyl, trifluoromethoxy, methylthio, ethylthio or methylsulforyl;
- Ar2 is C3-C10-cycloalkyl, a thienyl group or a phenyl group optionally substituted by one or two moieties selected from methyl, ethyl, fluorine, chlorine, bromine, cyano, methoxy, ethoxy, methoxymethyl, trifluoromethyl, trifluoromethoxy, methylthio, ethylthio or methylsulforyl;
- in compounds wherein R1 is an optionally substituted phenyl group, Ar2 may be directly linked to R1 by a CH2, CH2CH2, CH:CH, OCH2 or CH2O group;
- Ar3 is C3-C10-cycloalkyl, a thienyl group or a phenyl group substituted by one or two moieties selected from methyl, ethyl, fluorine, chlorine, bromine, cyano, methoxy, ethoxy, methoxymethyl, trifluoromethyl, trifluoromethoxy, methylthio, ethylthio, methylsulfonyl;
- in compounds wherein Ar2 is an optionally substituted phenyl group R may be linked to Ar2 by a CH2, CH2CH2, CH:CH, OCH2 of CH2O group.
- Ar4 is a biphenyl group optionally substituted by one or two moieties selected from fluorine, chlorine, bromine, methyl, ethyl, cyano, methoxy, ethoxy, methoxymethyl, trifluoromethyl, trifluoromethoxy, methylthio, ethylthio or methylsulforyl;
- n is 0, 1 or 2;
- L is a hydrocarbon linking group of 2 to 20 carbon atoms which may be optionally interrupted by O, N, or CO, and is aptly a group of the form:
- Y1—Y2—Y3
- wherein:
- Y2 is not present or is a group of the formula CH—Y4-Q or —N—Y4-Q where Q independently is a group as defined above and Y4 is a bond or a hydrocarbon linking group of 1 to 8 carbon atoms optionally interrupted by O, NH or CO;
- Y1 is attached to the NH group shown is formula (I) and is a hydrocarbon linking group of 2 to 20 carbon atoms optionally containing an ether oxygen atom or;
- Y3 is not present or is selected from 0 or a group NR2 where R2 is a hydrogen atom or an alkyl group of 2 to 3 carbon atoms optionally linked to a carbon atom within Y1 or Y2 to form a ring or 4, 5, 6 or 7 ring atoms;
- and
- represents a group of the formula:
- or a pharmaceutically acceptable salt thereof.
17 more elements
Dependencies are inferred from the claim text.