IP Library Granted Patent US 8,252,806
Granted Patent B2
US 8,252,806 · App. 11/886,341 · Granted Aug 28, 2012

Potassium channel modulating agents and their medical use

Assignee: Neurosearch A/S
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Quick Facts
Patent No.
US 8,252,806
App. No.
11/886,341
Granted
Aug 28, 2012
Kind
B2
Abstract

This invention relates to novel potassium channel modulating agents, and their use in the preparation of pharmaceutical compositions. Moreover the invention is directed to pharmaceutical compositions useful for the treatment or alleviation of diseases or disorders associated with the activity of potassium channels, in particular respiratory diseases, epilepsy, convulsions, vascular spasms, coronary artery spasms, renal disorders, polycystic kidney disease, bladder spasms, urinary incontinence, bladder outflow obstruction, irritable bowel syndrome, gastrointestinal dysfunction, secretory diarrhoea, ischaemia, cerebral ischaemia, ischaemic heart disease, angina pectoris, coronary heart disease, traumatic brain injury, psychosis, schizophrenia, anxiety, depression, dementia, memory and attention deficits, Alzheimer's disease, dysmenorrhea, narcolepsy, Reynaud's disease, intermittent claudication, Sjorgren's syndrome, migraine, arrhythmia, hypertension, absence seizures, myotonic muscle dystrophia, xerostomi, diabetes type II, hyperinsulinemia, premature labour, baldness, cancer, immune suppression or pain.

Claims (101)

1. A pyrazolyl-quinazoline compound of Formula I

or a pharmaceutically acceptable salt thereof, wherein

n is 0 or 1;

X represents 0, S or NR′; wherein

R′ represents hydrogen or alkyl;

Y represents alkyl or alkenyl, or a monocyclic or polycyclic, carbocyclic group selected from cycloalkyl, phenyl, naphthyl, 1,2,3,4-tetrahydro-naphthyl and indanyl, or a monocyclic or polycyclic heterocyclic group selected from pyridinyl, indolyl tetrahydro-pyranyl and guinolinyl, or heterocyclic group, which carbocyclic or heterocyclic groups may optionally be substituted one or more times with substituents selected from the group consisting of alkyl, halo, haloalkyl, alkoxy, methylenedioxy, phenyl and morpholinyl;

or, when n is 0 and X is NR′, Y together with R′ and together with the nitrogen to which they are attached form a piperidinyl ring; and

R 1 , R 2 and R 3 independently of each other, represent hydrogen or alkyl.

2. The pyrazolyl-quinazoline compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein

n is 0.

3. The pyrazolyl-quinazoline compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein

X represents NR′; wherein

R′ represents hydrogen or alkyl.

4. The pyrazolyl-quinazoline compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein

n is 0;

X represents NR′; and

R′ together with Y and together with the nitrogen to which they are attached form a piperidinyl ring.

5. The pyrazolyl-quinazoline compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein

Y represents alkyl or alkenyl, or a monocyclic or polycyclic, carbocyclic or heterocyclic group, selected from cycloalkyl, phenyl, naphthyl, 1,2,3,4-tetrahydro-naphthyl and indanyl, which carbocyclic groups may optionally be substituted one or more times with substituents selected from the group consisting of alkyl, halo, haloalkyl, alkoxy, methylenedioxy, phenyl and morpholinyl.

6. The pyrazolyl-quinazoline compound of claim 5 , or a pharmaceutically acceptable salt thereof, wherein Y represents

alkyl, alkenyl or cycloalkyl.

7. The pyrazolyl-quinazoline compound of claim 5 , or a pharmaceutically acceptable salt thereof, wherein Y represents

a monocyclic or polycyclic carbocyclic group selected from phenyl, naphthyl, 1,2,3,4-tetrahydro-naphthyl and indanyl, which carbocyclic groups may optionally be substituted one or more times with substituents selected from the group consisting of alkyl, halo, haloalkyl, alkoxy, methylenedioxy, phenyl and morpholinyl.

8. The pyrazolyl-quinazoline compound of claim 5 , or a pharmaceutically acceptable salt thereof, wherein Y represents

a heterocyclic group selected from pyridinyl, indolyl, tetrahydro-pyranyl and quinolinyl.

9. The pyrazolyl-quinazoline compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein

R 1 , R 2 and R 3 independently of each other, represent hydrogen or alkyl.

10. The pyrazolyl-quinazoline compound of claim 9 , or a pharmaceutically acceptable salt thereof, wherein

R 1 and R 2 independently of each other, represent hydrogen or alkyl; and

R 3 represents hydrogen.

11. The pyrazolyl-quinazoline compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein

n is 0;

X represents O, S or NR′; wherein R′ represents hydrogen, methyl, ethyl or propyl;

Y represents alkyl, alkenyl, cycloalkyl, alkyl-cycloalkyl; and

R 1 and R 2 represent methyl or isopropyl; and

R 3 represents hydrogen.

12. The pyrazolyl-quinazoline compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein

n is 0 or 1;

X represents NH;

Y represents phenyl, optionally substituted one or two times with substituents selected from the group consisting of alkyl, halo, haloalkyl, alkoxy, methylenedioxy, phenyl and morpholinyl;

R 1 and R 2 represent methyl or isopropyl; and

R 3 represents hydrogen.

13. The pyrazolyl-quinazoline compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein

n is 0;

X represents NR′; and

R′ together with Y and together with the nitrogen to which they are attached form a piperidinyl ring; and

R 1 and R 2 , independently of each other, represent methyl, ethyl or propyl; and

R 3 represents hydrogen.

14. The pyrazolyl-quinazoline compound of claim 1 , which is

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-propylamine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-ethylamine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-diethyl-amine;

Butyl-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

Allyl-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

Cyclopropyl-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

Cyclopentyl-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

Cyclohexyl-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

Cycloheptyl-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

Cyclooctyl-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

2-(3,5-Dimethyl-pyrazol-1-yl)-4-piperidin-1-yl-quinazoline;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-piperidin-4-yl-amine;

Benzyl-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

(4-Chloro-benzyl)-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

(3,4-Difluoro-benzyl)-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-furan-2-ylmethyl-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-thiophen-2-ylmethyl-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-phenyl-amine;

(4-Chloro-phenyl)-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

(3-Chloro-phenyl)-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

(2-Chloro-phenyl)-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

(3,4-Dichloro-phenyl)-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

(4-Bromo-phenyl)-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-(4-trifluoromethyl-phenyl)-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-(3-trifluoromethyl-phenyl)-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-(3-methoxy-phenyl)-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-p-tolyl-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-m-tolyl-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-o-tolyl-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-naphthalen-2-yl-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-(1,2,3,4-tetrahydro-naphthalen-1-yl)-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-(2-pyrrolidin-1-yl-ethyl)-amine;

Cyclohexyl-[2-(3-methyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

S-[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-(S)-1,2,3,4-tetrahydro-naphthalen-1-yl-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-(1-ethyl-propyl)-amine;

[2-(3,5-Diisopropyl-pyrazol-1-yl)-quinazolin-4-yl]-(4-methyl-cyclohexyl)-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-pyridin-2-yl-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-(4-methyl-cyclohexyl)-amine;

(4-tert-Butyl-cyclohexyl)-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-(tetrahydro-pyran-4-yl)-amine;

Cyclohexyl-[2-(3,5-diisopropyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-indan-2-yl-amine;

Benzo[1,3]dioxol-5-yl-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

(3,5-Bis-trifluoromethyl-phenyl)-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-(4-morpholin-4-yl-phenyl)-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-quinolin-8-yl-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-(4-iodo-phenyl)-amine;

Biphenyl-4-yl-[2-(3,5-dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-amine;

[2-(3,5-Dimethyl-pyrazol-1-yl)-quinazolin-4-yl]-(1H-indol-7-yl)-amine; or

Cyclohexyl-(2-pyrazol-1-yl-quinazolin-4-yl)-amine;

or a pharmaceutically acceptable salt thereof.

15. A pharmaceutical composition comprising a therapeutically effective amount of a pyrazolyl-quinazoline compound according to claim 1 , or a pharmaceutically acceptable addition salt thereof, together with at least one pharmaceutically-acceptable carrier or diluent.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2023
From: CADENT THERAPEUTICS, INC.
To: NOVARTIS AG
Reel/Frame 062321/0739 →
CHANGE OF NAME Recorded Jan 3, 2023
From: LUC THERAPEUTICS, INC.
To: CADENT THERAPEUTICS, INC.
Reel/Frame 062265/0889 →
MERGER Recorded Dec 20, 2022
From: ATAXION, INC.
To: LUC THERAPEUTICS, INC.
Reel/Frame 062155/0043 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 6, 2013
From: ANIONA APS
To: ATAXION, INC.
Reel/Frame 030946/0329 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 20, 2013
From: NEUROSEARCH A/S
To: ANIONA APS
Reel/Frame 030049/0894 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 2, 2007
From: ERIKSEN, BIRGITTE L.; TEUBER, LENE; HOUGAARD, CHARLOTTE; SORENSEN, ULRIK SVANE
To: NEUROSEARCH A/S
Reel/Frame 019905/0260 →
Priority Claims (1)
DK 2005 00366 · Mar 14, 2005 · national
Continuity (2)
Provisional Application 60661149 · Mar 14, 2005
Related Publication 20080275045A1 · Nov 6, 2008