IP Library Granted Patent US 8,293,775
Granted Patent B2
US 8,293,775 · App. 11/569,605 · Granted Oct 23, 2012

Benzoxazolone derivatives, processes for preparing them and their uses

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Quick Facts
Patent No.
US 8,293,775
App. No.
11/569,605
Granted
Oct 23, 2012
Kind
B2
Abstract

The present invention relates to benzoxazolone derivatives, processes for preparing them, pharmaceutical compositions containing them and their use as pharmaceuticals, in the treatment of movement disorders, in particular in Parkinson's disease.

Claims (38)

1. A method for the symptomatic treatment of Parkinson's disease or dopa-responsive dystonia in a patient, the method comprising administering to the patient an effective amount of a compound according to formula Ia:

or a pharmaceutically acceptable salt thereof, wherein

R 1 is selected from hydrogen or C 1-4 -alkyl unsubstituted or substituted by hydroxy;

R 2 is selected from hydrogen or C 1-4 -alkyl unsubstituted or substituted by hydroxy;

R 3 is selected from hydrogen or unsubstituted C 1-4 -alkyl;

R 3a is selected from hydrogen or unsubstituted C 1-4 -alkyl;

R 4 is selected from hydrogen, halogen, or C 1-4 -alkoxy unsubstituted or substituted by a phenyl group;

R 5 is selected from hydrogen, halogen, or C 1-4 -alkoxy unsubstituted or substituted by a phenyl group;

R 6 is selected from hydrogen, halogen, or C 1-4 -alkoxy unsubstituted or substituted by a phenyl group; and

R 7 is selected from hydrogen, halogen, or C 1-4 -alkoxy unsubstituted or substituted by a phenyl group;

with the proviso that the compound is not 2-(6-bromo-2-oxo-1,3-benzoxazol-3(2H)-yl)acetamide.

2. The method according to claim 1 wherein

R 1 is hydrogen;

R 2 is hydrogen;

R 3 is selected from hydrogen or unsubstituted C 1-4 -alkyl;

R 3a is selected from hydrogen or unsubstituted C 1-4 -alkyl;

R 4 is hydrogen;

R 5 is selected from hydrogen, bromo or chloro;

R 6 is selected from hydrogen, bromo or chloro; and

R 7 is hydrogen;

with the proviso that the compound is not 2-(6-bromo-2-oxo-1,3-benzoxazol-3(2H)-yl)acetamide.

3. The method according to claim 1 wherein the compound is selected from

2-(6-bromo-2-oxo-1,3-benzoxazol-3(2H)-yl)-N,N-dimethylacetamide;

2-(2-oxo-1,3-benzoxazol-3(2H)-yl)acetamide;

2-(6-chloro-2-oxo-1,3-benzoxazol-3(2H)-yl)acetamide;

2-(6-chloro-2-oxo-1,3-benzoxazol-3(2H)-yl)-N,N-dimethylacetamide; and

N,N-dimethyl-2-(2-oxo-1,3-benzoxazol-3(2H)-yl)acetamide.

4. The method according to claim 1 wherein

R 1 is hydrogen;

R 2 is hydrogen;

R 3 is selected from hydrogen or methyl;

R 3a is selected from hydrogen or methyl;

R 4 is hydrogen;

R 5 is hydrogen;

R 6 is selected from hydrogen, fluoro, chloro, or methoxy; and

R 7 is selected from hydrogen, fluoro, chloro, or bromo;

with the proviso that if R 7 is hydrogen, then R 6 is not hydrogen or chloro.

5. The method according to any one of claim 1 - 3 or 4 wherein the method is for the symptomatic treatment of Parkinson's disease.

Assignments (3)
CONFIRMATORY ASSIGNMENT Recorded Jun 10, 2016
From: UCB PHARMA, S.A.
To: UCB BIOPHARMA SPRL
Reel/Frame 038953/0312 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 12, 2008
From: UCB, S.A.
To: UCB PHARMA, S.A.
Reel/Frame 021823/0435 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 10, 2007
From: STARCK, JEAN-PHILIPPE; KENDA, BENOIT
To: UCB, S.A.
Reel/Frame 019142/0061 →