IP Library Granted Patent US 11,707,476
Granted Patent B2
US 11,707,476 · App. 17/386,686 · Granted Jul 25, 2023

Catecholamine prodrugs for use in the treatment of parkinson's disease

Inventors: Klaus Gjervig Jensen (Valby, DK); Lisbet Kværnø (Valby, DK); Morten Jørgensen (Valby, DK); Martin Juhl (Valby, DK)
Assignee: H. Lundbeck A/S
A61K31/706A61K31/473A61P25/00C07D405/12C07D405/14
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,707,476
App. No.
17/386,686
Granted
Jul 25, 2023
Kind
B2
Abstract

The present invention provides compounds of formula (Id) that are prodrugs of catecholamine for use in treatment of neurodegenerative diseases and disorders. The present invention also provides pharmaceutical compositions comprising compounds of the invention and methods of treating neurodegenerative or neuropsychiatric diseases and disorders using the compounds of the invention, in particular Parkinson's disease.

Claims (39)

1. A method for the treatment of a neurodegenerative disease or disorder; which method comprises the administration of a therapeutically effective amount of a compound according to formula (Id)

or a pharmaceutically acceptable salt thereof to a patient in need thereof;

wherein

R1 is H and R2 is selected from one of the substituents (i) and (ii) below; or

R1 is selected from one of the substituents (i) and (ii) below and R2 is H; or

R1 and R2 are both represented by substituent (i) below; or

R1 and R2 are both represented by substituent (ii) below; or

R1 is substituent (i) and R2 is substituent (ii); or

R1 is substituent (ii) and R2 is substituent (i);

wherein * indicates the attachment point; and

wherein the carbon atom at the attachment point on substituent (i) is in the S-configuration.

2. The method according to claim 1 , wherein the neurodegenerative disease or disorder is Parkinson's Disease.

3. The method according to claim 1 , further comprising administering to the patient an additional agent useful in the treatment of the neurodegenerative disease or disorder.

4. The method according to claim 3 , wherein said additional agent is useful in the treatment of Parkinson's disease.

5. The method according to claim 1 , wherein said compound of formula (Id) is the compound represented by formula (Id-ia) below

or a pharmaceutically acceptable salt thereof.

6. The method according to claim 1 , wherein said compound of formula (Id) is the compound represented by formula (Id-ib) below

or a pharmaceutically acceptable salt thereof.

7. The method according to claim 1 , wherein said compound of formula (Id) is the compound represented by formula (Id-iab) below

or a pharmaceutically acceptable salt thereof.

8. The method according to claim 2 , wherein said compound of formula (Id) is the compound represented by formula (Id-ia) below

or a pharmaceutically acceptable salt thereof.

9. The method according to claim 2 , wherein said compound of formula (Id) is the compound represented by formula (Id-ib) below

or a pharmaceutically acceptable salt thereof.

10. The method according to claim 2 , wherein said compound of formula (Id) is the compound represented by formula (Id-iab) below

or a pharmaceutically acceptable salt thereof.

11. The method according to claim 3 , wherein said compound of formula (Id) is the compound represented by formula (Id-ia) below

or a pharmaceutically acceptable salt thereof.

12. The method according to claim 3 , wherein said compound of formula (Id) is the compound represented by formula (Id-ib) below

or a pharmaceutically acceptable salt thereof.

13. The method according to claim 3 , wherein said compound of formula (Id) is the compound represented by formula (Id-iab) below

or a pharmaceutically acceptable salt thereof.

14. The method according to claim 4 , wherein said compound of formula (Id) is the compound represented by formula (Id-ia) below

or a pharmaceutically acceptable salt thereof.

15. The method according to claim 4 , wherein said compound of formula (Id) is the compound represented by formula (Id-ib) below

or a pharmaceutically acceptable salt thereof.

16. The method according to claim 4 , wherein said compound of formula (Id) is the compound represented by formula (Id-iab) below

or a pharmaceutically acceptable salt thereof.

17. A compound, or a pharmaceutically acceptable salt thereof, wherein the compound is (4aR,10aR)-1-propyl-6-((triisopropylsilyl)oxy)-1,2,3,4,4a,5,10,10a-octahydrobenzo[g]quinolin-7-ol.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 2, 2021
From: JENSEN, KLAUS GJERVIG; KVAERNO, LISBET; JORGENSEN, MORTEN; JUHL, MARTIN
To: H. LUNDBECK A/S
Reel/Frame 057367/0904 →
Priority Claims (1)
DK PA201700674 · Nov 24, 2017 · national
Continuity (3)
Continuation 16872802 · May 12, 2020
Continuation 16198917 · Nov 23, 2018
Related Publication 20220257623A1 · Aug 18, 2022
Cited By (8)
US 12,226,428 US 12,319,710 US 12,384,765 US 12,391,650 US 12,398,106 US 12,398,169 US 12,421,271 US 12,479,801