IP Library Granted Patent US 11,420,955
Granted Patent B2
US 11,420,955 · App. 17/193,678 · Granted Aug 23, 2022

Compounds as neuronal histamine receptor-3 antagonists and uses thereof

Inventors: Jia-Ning Xiang (Wuhan, CN); 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 11,420,955
App. No.
17/193,678
Granted
Aug 23, 2022
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 (50)

1. A method of treating narcolepsy associated with a viral infection in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound having the structure:

or a pharmaceutically acceptable salt thereof, wherein,

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

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

2. The method of claim 1 , wherein,

R 1 is selected from hydrogen and methyl; and

R 2 is selected from hydrogen, hydroxyl, and methoxy.

3. The method of claim 1 , wherein the compound is 2-methyl-3-(4-(3-(pyrrolidin-1-yl)propoxy)phenyl)-6-(pentafluorosulfanyl) quinazolin-4(3H)-one (I) or a pharmaceutically acceptable salt thereof:

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

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

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

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

3-(2-hydroxy-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)-2-methyl-6-(pentafluoro-16-sulfaneyl)quinazolin-4(3H)-one (VIII);

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

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

or a pharmaceutically acceptable salt of any of the foregoing.

5. The method of claim 1 , wherein administering comprises administering a pharmaceutical composition comprising the compound having the structure:

or a pharmaceutically acceptable salt thereof, wherein,

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

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

6. 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 thereof a therapeutically effective amount of a compound having the structure:

or a pharmaceutically acceptable salt thereof, wherein,

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

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

7. The method of claim 6 , wherein,

R 1 is selected from hydrogen and methyl; and

R 2 is selected from hydrogen, hydroxyl, and methoxy.

8. The method of claim 6 , wherein the compound is 2-methyl-3-(4-(3-(pyrrolidin-1-yl)propoxy)phenyl)-6-(pentafluorosulfanyl) quinazolin-4(3H)-one (I) or a pharmaceutically acceptable salt thereof:

9. The method of claim 6 , wherein the compound is selected from:

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

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

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

3-(2-hydroxy-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)-2-methyl-6-(pentafluoro-16-sulfaneyl)quinazolin-4(3H)-one (VIII);

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

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

or a pharmaceutically acceptable salt of any of the foregoing.

10. The method of claim 6 , wherein administering comprises administering a therapeutically effective amount of a pharmaceutical composition comprising the compound having the structure:

or a pharmaceutically acceptable salt thereof, wherein,

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

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

11. A method of treating narcolepsy associated with a viral infection in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound selected from:

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

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

a pharmaceutically acceptable salt of any of the foregoing.

12. The method of claim 11 , wherein administering comprises administering a therapeutically effective amount of a pharmaceutical composition comprising the compound.

13. 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 thereof a therapeutically effective amount of a compound selected from:

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

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

a pharmaceutically acceptable salt of any of the foregoing.

14. The method of claim 13 , wherein administering comprises administering a therapeutically effective amount of a pharmaceutical composition comprising the compound.

Assignments (2)
CHANGE OF NAME Recorded May 4, 2021
From: XW LABORATORIES INC.
To: XWPHARMA LTD.
Reel/Frame 056177/0619 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2021
From: XIANG, JIA-NING; XU, XUESONG; FENG, YI; ENG, WAI-SI
To: XW LABORATORIES INC.
Reel/Frame 055510/0529 →
Continuity (5)
Continuation 16909779 · Jun 23, 2020
Continuation 16793139 · Feb 18, 2020
Division 16587344 · Sep 30, 2019
Continuation PCTCN2018109115 · Sep 30, 2018
Related Publication 20210188808A1 · Jun 24, 2021