Pyridine Compounds For The Treatment Of Prostaglandin Mediated Diseases
AssigneeGlaxo Group Limited
InventorsGerard Martin Paul Giblin, Adrian Hall, David Nigel Hurst, Derek Anthony Rawlings, Tiziana Scoccitti
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Abstract
Compounds of formula (I) or a pharmaceutically acceptable derivative thereof: wherein X, Y, Z, R2a, R2b, R3a, R3b, R8, R9, and Rx are as defined in the specification, a process for the preparation of such compounds, pharmaceutical compositions comprising such compounds and the use of such compounds in medicine (EP, —receptor antagonists).
Claims18
A compound of formula (I):
- wherein:
- X is N and Y is CH, or X is CH and Y is N;
- Z is O, S, SO or SO2;
- R1 is CO2H, CONHSO2R6, CH2CO2H, NR4COR7, tetrazole or CH2tetrazole;
- R2a and R2b are each independently selected from hydrogen, halo, CN, SO2alkyl, SR5, NO2, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted aryl, and optionally substituted heteroaryl;
- R3a and R3b are each independently selected from hydrogen, halo, optionally substituted alkyl, optionally substituted alkoxy, or NR10R11;
- Rx is optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted CQaQb-heterocyclyl, optionally substituted CQaQb-bicyclic heterocyclyl, or optionally substituted CQaQb-aryl;
- R4 is hydrogen or an optionally substituted alkyl;
- R5 is hydrogen or an optionally substituted alkyl;
- R6 is optionally substituted alkyl, optionally substituted aryl, or optionally substituted heterocyclyl;
- R7 is optionally substituted alkyl, optionally substituted heterocyclyl, optionally substituted aryl, optionally substituted alkoxy, optionally substituted heterocyclyloxy or optionally substituted aryloxy;
- R8 is hydrogen, fluorine or alkyl;
- R9 is hydrogen, hydroxy, fluorine or alkyl;
- or R8 and R9 together with the carbon to which they are attached form a cycloalkyl ring, optionally containing up to one heteroatom selected from O, S, NH and N-alkyl;
- or R8 and
- R9 together with the carbon to which they are attached form a carbonyl group;
- Qa and Qb are each independently selected from hydrogen, CH3 and fluorine;
- R10 and R11 are each independently selected from hydrogen or alkyl;
- or R10 and R11 together with the nitrogen to which they are attached form an aliphatic heterocyclic ring, optionally containing an additional heteroatom selected from O, S, NH and N-alkyl;
- and derivatives thereof.
The compound of formula (I) which is 6-[(5-chloro-2-{[(4-chloro-2-fluorophenyl)methyl]oxy}phenyl)methyl]-2-pyridinecarboxylic acid or a pharmaceutically acceptable derivative thereof.
Dependencies are inferred from the claim text.