IP Library Granted Patent US 7,087,593
Granted Patent B2
US 7,087,593 · App. 10/262,517 · Granted Aug 8, 2006

Benzimidazolidinone derivatives as muscarinic agents

Assignee: ACADIA Pharmaceuticals Inc.
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Quick Facts
Patent No.
US 7,087,593
App. No.
10/262,517
Granted
Aug 8, 2006
Kind
B2
Abstract

Benzimidazolidinone derivative compounds, which increase acetylcholine signaling or effect in the brain, and highly selective muscarinic agonists, particularly for the M 1 and/or M 4 receptor subtypes, pharmaceutical compositions comprising the same, as well as methods of treating psychosis using these compounds are disclosed.

Claims (34)

1. A compound of Formula I

or a pharmaceutically acceptable salt or prodrug thereof, wherein

X is selected from the group consisting of C, O, N and S

Z is selected from the group consisting of CH and N

Y is selected from the group consisting of ═O, ═N and ═S or tautomers thereof;

SPU is a spacer unit providing a distance d between Z and N wherein

—SPU— is a biradical selected from the group consisting of —(CR 6 R 7 ) n —A— and —C 3-8 -cycloalkyl-

wherein n is in the range 1 to 5, such as 1, 2, 3, 4, or 5 and

A is absent or an optionally substituted —C 3-8 -cycloalkyl;

N together with R 1 and R 2 form a heterocyclic ring wherein said heterocyclic ring is 8-azabicyclo[3.2.1]octane

and wherein the heterocyclic ring is substituted with one or more substituents R 4 selected from the group consisting of halogen, C 1-8 -alkyl, C 3-8 -cycloalkyl, C 1-8 -alkoxy, C 1-8 -alkylcarbonyl, C 1-8 -alkylidene, C 2-8 -alkenyl, C 2-8 -alkynyl, C 1-6 -alkyloxyimino, and C 1-6 -alkyloxyamino each of which may be optionally substituted with a substituent R 5

and wherein at least one of said substituents R 4 is R 4 ′ selected from the group consisting of C 1-8 -alkyl, C 3-8 -cycloalkyl, C 1-8 -alkoxy, C 1-8 -alkylcarbonyl, C 1-8 -alkylidene, each of which may be optionally substituted with a substituent R 5 ;

R 5 is selected from the group consisting of hydrogen, halogen, hydroxy, C 1-8 -alkyl, C 1-8 -alkoxy, C 3-8 -cycloalkyl, C 3-8 -heterocyclyl, C 1-8 -alkylcarbonyl, C 1-8 -alkylidene, C 2-8 -alkenyl and C 2-8 -alkynyl;

R X may be absent or selected from the group consisting of hydrogen, optionally substituted C 1-8 -alkyl, optionally substituted C 3-8 -cycloalkyl, optionally substituted C 2-8 -alkenyl, optionally substituted C 2-8 -alkynyl, CH 2 —N(R 5 )(R 5 ), CH 2 —OR 5 , CH 2 —SR 5 , CH 2 —O—C(═O)R 5 , CH 2 —O—C(═S)R 5 ;

R 3 may be present 0–4 times and selected from the group consisting of halogen, hydroxy, optionally substituted C 1-8 -alkyl, C 1-8 -alkoxy, optionally substituted C 1-8 -alkylidene, optionally substituted C 2-8 -alkenyl, optionally substituted C 2-8 -alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted C 3-8 -cycloalkyl, optionally substituted C 3-8 -heterocyclyl, and optionally substituted C 1-8 -alkylcarbonyl;

each R 6 and each R 7 is optionally and independently selected from the group consisting of hydrogen, halogen, hydroxy, optionally substituted C 1-8 -alkyl, C 1-8 -alkoxy, optionally substituted C 1-8 -alkylidene, optionally substituted C 2-8 -alkenyl, optionally substituted C 2-8 -alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted C 3-8 -cycloalkyl, optionally substituted C 3-8 -heterocyclyl, and optionally substituted C 1-8 -alkylcarbonyl.

2. The compound of claim 1 , wherein Z is N.

3. The compound of claim 2 , wherein X is selected from the group consisting of N, S, and O.

4. The compound of claim 3 , wherein —Y is ═O.

5. The compound of claim 1 , wherein R 4 ′ is selected from the group consisting of C 1-8 -alkyl, C 1-8 -alkoxy, C 3-8 -cycloalkyl, C 1-8 -alkylidene, each of which may be optionally substituted with a substituent R 5 .

6. The compound of claim 1 , wherein R 4 is selected from the group consisting of C 3-8 -alkyl, C 3-8 -alkoxy, and C 3-8 -alkylidene, each of which may be optionally substituted with a substituent R 5 wherein R 5 is selected from the group consisting of hydrogen, halogen, hydroxy and C 1-8 -alkyl.

7. The compound of claim 1 , wherein R 4 is selected from the group consisting of an optionally substituted butyl, an optionally substituted pentyl, an optionally substituted propyloxy, and 3-(C 1-8 -alkyl)-butylidene.

8. A pharmaceutical composition comprising a compound according to claim 1 , together with pharmaceutically acceptable carriers or excipients.

9. A method of treating mental disease or disorder in a mammal comprising identifying a mammal in need thereof and administering at least one compound of claim 1 to said mammal.

10. The method of claim 9 , wherein the mental disorder is selected from the group consisting of cognitive impairment, forgetfulness, confusion, memory loss, attentional deficits, deficits in visual perception, depression, sleep disorders, and psychosis.

11. The method of claim 9 , wherein the mental disorder is selected from the group consisting of neurodegenerative diseases, Alzheimer's disease, Parkinson's disease, schizophrenia, Huntington's chorea, Friederich's ataxia, Gilles de la Tourette's Syndrome, Down Syndrome, Pick disease, dementia, clinical depression, age-related cognitive decline, attention-deficit disorder, and sudden infant death syndrome.

12. A method of treating a disease or disorder associated with increased intraocular pressure in a mammal comprising identifying a mammal in need thereof and administering at least one compound of claim 1 to said mammal.

13. A method of increasing an activity of a cholinergic receptor comprising contacting the cholinergic receptor or a system containing the cholinergic receptor with an effective amount of at least one compound of claim 1 .

14. The method of claim 13 , wherein the compound is a cholinergic agonist.

15. The method of claim 14 , wherein the compound is selective for one or both of a M 1 and M 4 muscarinic receptor subtypes.

16. The method of claim 13 , wherein the compound further acts as a D 2 antagonist or D 2 inverse agonist.

17. A method of treating pain in a mammal, comprising administering an effective amount of a compound of claim 1 to said mammal.

18. A method of prophylactic or curative treatment of psychosis or alleviation of symptoms of psychosis in a mammal, comprising administering an effective amount of a compound of claim 1 to said mammal.

19. A method of modulating the progression or formation of amyloid plaques in an individual susceptible to or affected by Alzheimer's Disease, comprising administering an effective amount of a compound of claim 1 , said effective amount sufficient to modulate amyloid precursor protein processing.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2002
From: KELLY, NICHOLAS MICHAEL; KOCH, KRISTIAN NORUP; TOLF, BO-RAGNAR
To: ACADIA PHARMACEUTICALS, INC.
Reel/Frame 013603/0944 →
Continuity (2)
Provisional Application 6032675400 · Oct 2, 2001
Related Publication 20030100545A1 · May 29, 2003