IP Library Granted Patent US 12,172,980
Granted Patent B2
US 12,172,980 · App. 17/867,681 · Granted Dec 24, 2024

Compounds as neuronal histamine receptor-3 antagonists and uses thereof

Inventors: Jia-Ning Xiang (Fremont, CA); Xuesong Xu (Wuhan, CN); Yi Feng (Wuhan, CN); Wai-Si Eng (Maple Glen, PA)
Assignee: XWPHARMA LTD.
C07D401/12
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Quick Facts
Patent No.
US 12,172,980
App. No.
17/867,681
Granted
Dec 24, 2024
Kind
B2
Abstract

The present invention relates compounds of Formula (A) as H3R antagonists, as well as their preparation and uses, and further relates pharmaceutical compositions comprising these compounds and their uses as modulators of Histamine 3 Receptor (H3R) functions. The present invention also relates to the uses of the compounds or pharmaceutical compositions in treating or preventing certain disorders and diseases which relate to H3R functions in humans.

Claims (46)

1. A compound selected from a compound of any one of Formula (1) to Formula (4):

or a pharmaceutically acceptable salt thereof, wherein,

R 1 is selected from hydrogen and C 1-3 alkyl;

R 2 is selected from hydrogen, hydroxyl, and C 1-3 alkoxy; and

R 3 is selected from cyclopropyl, cyclopentyl, tetrahydro-2H-pyran-4-yl, and 1-methylpiperidin-4-yl.

2. The compound of claim 1 , wherein,

the compound is selected from a compound of Formula (2) and (3) or a pharmaceutically acceptable salt thereof;

R 1 is selected from hydrogen and methyl; and

R 2 is selected from hydrogen and methoxy.

3. The compound of claim 1 , wherein,

the compound is selected from a compound of Formula (2) and (3) or a pharmaceutically acceptable salt thereof;

R 1 is methyl; and

R 2 is selected from hydrogen and methoxy.

4. The compound of claim 1 , wherein,

the compound is selected from a compound of Formula (2) and (3) or a pharmaceutically acceptable salt thereof;

R 1 is hydrogen; and

R 2 is selected from hydrogen and methoxy.

5. The compound of claim 1 , wherein,

the compound is selected from a compound of Formula (2) and (3) or a pharmaceutically acceptable salt thereof;

R 1 is selected from hydrogen and methyl; and

R 2 is hydrogen.

6. The compound of claim 1 , wherein,

the compound is a compound of Formula (1) or a pharmaceutically acceptable salt of any of the foregoing; and

R 2 is selected from hydrogen and methoxy.

7. The compound of claim 1 , wherein,

the compound is a compound of Formula (4) or a pharmaceutically acceptable salt thereof; and

R 2 is selected from hydrogen and methoxy.

8. The compound of claim 1 , wherein the compound is selected from:

3-(4-(3-(azepan-1-yl)propoxy)phenyl)-2-methyl-6-(pentafluorosulfanyl) quinazolin-4(3H)-one (III);

(S)-2-methyl-3-(4-(3-(3-methylpiperidin-1-yl)propoxy)phenyl)-6-(pentafluorosulfanyl)quinazolin-4(3H)-one (V);

2-methyl-3-(4-(3-(3-methylpyrrolidin-1-yl)propoxy)phenyl)-6-(pentafluorosulfanyl)quinazolin-4(3H)-one (VII);

(S)-3-(2-methoxy-4-(3-(3-methylpiperidin-1-yl)propoxy)phenyl)-2-methyl-6-(pentafluorosulfanyl)quinazolin-4(3H)-one (IX);

3-(2-methoxy-4-(3-(3-methylpyrrolidin-1-yl)propoxy)phenyl)-2-methyl-6-(pentafluorosulfanyl)quinazolin-4(3H)-one (XII);

3-(4-((1-cyclopropylpiperidin-4-yl)oxy)phenyl)-2-methyl-6-(pentafluorosulfanyl) quinazolin-4(3H)-one (XIV);

3-(4-((1-(cyclopentanecarbonyl)piperidin-4-yl)oxy)phenyl)-2-methyl-6-(pentafluorosulfanyl)quinazolin-4(3H)-one (XVI);

2-methyl-3-(4-((1-(1-methylpiperidine-4-carbonyl)piperidin-4-yl)oxy)phenyl)-6-(pentafluorosulfanyl)quinazolin-4(3H)-one (XX);

2-methyl-3-(4-((1-(tetrahydro-2H-pyran-4-carbonyl)piperidin-4-yl)oxy)phenyl)-6-(pentafluorosulfanyl)quinazolin-4(3H)-one (XXI); and

3-(2-methoxy-4-((1-(tetrahydro-2H-pyran-4-carbonyl)piperidin-4-yl)oxy) phenyl)-2-methyl-6-(pentafluorosulfanyl)quinazolin-4(3H)-one (XXII);

or a pharmaceutically acceptable salt of any of the foregoing.

9. A pharmaceutical composition comprising the compound of claim 1 .

10. A method of treating narcolepsy, cataplexy associated with narcolepsy, or narcolepsy associated with a viral infection in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 1 .

11. A method of treating a sleep disorder associated with obstructive sleep apnea or a sleep disorder associated with Parkinson's disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 1 .

12. A method of enhancing cognitive function associated with a central nervous system disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the compound of claim 1 .

13. A method of treating narcolepsy, cataplexy associated with narcolepsy, or narcolepsy associated with a viral infection in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the pharmaceutical composition of claim 9 .

14. A method of treating a sleep disorder associated with obstructive sleep apnea or a sleep disorder associated with Parkinson's disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the pharmaceutical composition of claim 9 .

15. A method of enhancing cognitive function associated with a central nervous system disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of the pharmaceutical composition of claim 9 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 19, 2022
From: XIANG, JIA-NING; XU, XUESONG; FENG, YI; ENG, WAI-SI
To: XWPHARMA LTD.
Reel/Frame 060540/0215 →
Continuity (6)
Continuation 17193678 · Mar 5, 2021
Continuation 16909779 · Jun 23, 2020
Continuation 16793139 · Feb 18, 2020
Division 16587344 · Sep 30, 2019
Continuation PCTCN2018109115 · Sep 30, 2018
Related Publication 20220380339A1 · Dec 1, 2022