IP Library Granted Patent US 8,680,079
Granted Patent B2
US 8,680,079 · App. 11/597,623 · Granted Mar 25, 2014

Tetrahydro-imidazo [1,5-A] pyridyin derivatives as aldosterone synthase inhibitors

Inventors: Peter Herold (Basel, CH); Robert Mah (Muttenz, CH); Vincenzo Tschinke (Binningen, CH); Christoph Schumacher (Bettingen, CH); Michael Quirmbach (Basel, CH)
Assignee: Novartis AG
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Quick Facts
Patent No.
US 8,680,079
App. No.
11/597,623
Granted
Mar 25, 2014
Kind
B2
Abstract

The application relates to novel heterocyclic compounds of the general formula (I) in which R, R 1 , R 2 , X, Y, Z and n have the meanings defined in the description, to a process for their preparation and to the use of these compounds as medicaments, in particular as aldosterone synthase inhibitors.

Claims (36)

1. A compound of the formula

in which

X is N;

Y is C;

Z is a bond;

R is hydrogen or methyl;

R 1 is benzofuranyl, benzothiophenyl, indazolyl, indolyl, pyrrolyl, or oxazolyl optionally mono- or di-substituted with substituents selected from the group consisting of halogen, cyano, trifluoromethoxy, trifluoromethyl, trimethylsilanyl, heterocyclyl and C 1-8 -alkylcarbonyl; or thiazolyl mono- or di-substituted with C 1-8 -alkylcarbonyl

R 2 is hydrogen, halogen or C 1 -C 8 alkyl;

n is 1;

or its salt, a pharmaceutically acceptable salt thereof, or compound in which one or more atoms are replaced by their stable, nonradioactive isotopes.

2. The compound according to claim 1 , wherein the compound is represented by the formula

where R, R 1 , R 2 and n are as indicated for compounds of the formula (I) according to claim 1 .

3. Method for the prevention, for delaying the progression or for the treatment of pathological states which are caused or partly caused by hyperaldosteronism, where a therapeutically effective amount of a compound of the formula (I) according to claim 1 is used.

4. Method for the prevention, for delaying the progression or for the treatment of pathological states which are caused or partly caused by excessive cortisol release, where a therapeutically effective amount of a compound of the formula (I) according to claim 1 is used.

5. A pharmaceutical product comprising a compound of the formula (I) according to claim 1 , and conventional excipients.

6. A pharmaceutical combination in the form of a product or of a kit composed of individual components consisting a) of a compound of the formula (I) according to claim 1 , and b) at least one pharmaceutical form whose active ingredient has a blood pressure-lowering, an inotropic, a metabolic or a lipid-lowering effect.

7. Method for the prevention, for delaying the progression or for the treatment of pathological states which are caused or partly caused by hyperaldosteronism, where a therapeutically effective amount of a compound of the formula (Ia) according to claim 2 is used.

8. Method for the prevention, for delaying the progression or for the treatment of pathological states which are caused or partly caused by excessive cortisol release, where a therapeutically effective amount of a compound of the formula (Ia) according to claim 2 is used.

9. A pharmaceutical product comprising a compound of the formula (Ia) according to claim 2 , and conventional excipients.

10. A pharmaceutical combination in the form of a product or of a kit composed of individual components consisting a) of a compound of the formula (Ia) according to claim 2 , and b) at least one pharmaceutical form whose active ingredient has a blood pressure-lowering, an inotropic, a metabolic or a lipid-lowering effect.

11. A compound selected from the group consisting of:

1-[5-(5,6,7,8-Tetrahydroimidazo[1,5-a]pyridin-8-yl)thiazol-2-yl)ethanone;

8-Benzo[b]thiophen-3-yl-5,6,7,8-tetrahydro-imidazo[1,5-a]pyridine;

8-Benzofuran-3-yl-5,6,7,8-tetrahydro-imidazo[1,5-a]pyridine;

8-Benzo[b]thiophen-2-yl-5,6,7,8-tetrahydro-imidazo[1,5-a]pyridine;

8-(2-Methyl-benzo[b]thiophen-3-yl)-5,6,7,8-tetrahydro-imidazo[1,5-a]pyridine;

8-(3-Methyl-benzo[b]thiophen-2-yl)-5,6,7,8-tetrahydro-imidazo[1,5-a]pyridine;

8-(1-Methyl-1H-indol-5-yl)-5,6,7,8-tetrahydro-imidazo[1,5-a]pyridine;

1,3-Dimethyl-5′,6′,7′,8′-tetrahydro-[6,8′]bi[imidazo[1,5-a]pyridinyl]; and

8-Benzo[b]thiophen-5-yl-5,6,7,8-tetrahydro-imidazo[1,5-a]pyridine.

12. The compound according to claim 1 , wherein the compound is represented by the formula

where R, R 1 , R 2 and n are as indicated for compounds of the formula (I) according to claim 1 .

13. A pharmaceutical product comprising a compound of the formula (Ib) according to claim 12 , and conventional excipients.

14. A pharmaceutical combination in the form of a product or of a kit composed of individual components consisting a) of a compound of the formula (Ib) according to claim 12 , and b) at least one pharmaceutical form whose active ingredient has a blood pressure-lowering, an inotropic, a metabolic or a lipid-lowering effect.

15. Method for the prevention, for delaying the progression or for the treatment of pathological states which are caused or partly caused by hyperaldosteronism, where a therapeutically effective amount of a compound of the formula (Ib) according to claim 12 is used.

16. Method for the prevention, for delaying the progression or for the treatment of pathological states which are caused or partly caused by excessive cortisol release, where a therapeutically effective amount of a compound of the formula (Ib) according to claim 12 is used.

Assignments (2)
MERGER Recorded Feb 9, 2010
From: SPEEDEL EXPERIMENTA AG
To: NOVARTIS AG
Reel/Frame 023920/0239 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 27, 2006
From: HEROLD, PETER; MAH, ROBERT; TSCHINKE, VINCENZO; SCHUMACHER, CHRISTOPH; QUIRMBACH, MICHAEL
To: SPEEDEL EXPERIMENTA AG
Reel/Frame 018618/0809 →
Priority Claims (1)
CH 915/04 · May 28, 2004 · national
Continuity (1)
Related Publication 20070225232A1 · Sep 27, 2007