IP Library Granted Patent US 7,595,331
Granted Patent B2
US 7,595,331 · App. 11/007,484 · Granted Sep 29, 2009

N-and O-substituted 4-[2-(diphenylmethoxy)-ethyl]-1-[(phenyl)methyl]piperidine analogs and methods of treating CNS disorders therewith

Assignee: Wayne State University
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Quick Facts
Patent No.
US 7,595,331
App. No.
11/007,484
Granted
Sep 29, 2009
Kind
B2
Abstract

N- and O-substituted 4[2-diaromaticmethoxy and methylamino)alkyl]piperidines exhibit high CNS activity with respect to the dopamine transporter (DAT) and serotonin transporter (SERT). Preferred compounds exhibit highly differential behavior as between the DAT and SERT and between the DAT and the norepinephrine transporter (NET). The compounds have utility in treating CNS disorders, including but not limited to cocaine addiction, depression, and Parkinson's disease.

Claims (41)

1. Compounds exhibiting CNS activity in mammalian species, said compounds having the formula:

wherein A in formulae (I) is

B is

X is selected from the group consisting of N, —NH—, —NR 4 —, —0—, and —S—; R 4 is C 1-4 alkyl, NH 2, C 1-4 hydroxyalkyl, halogenated C 1-4 alkyl, C 2-4 alkenyl, C 2-4 hydroxyalkenyl, halogenated C 2-4 alkenyl, C 2-4 and alkynyl, and C 2-4 halogenated alkynyl; Y is -NH 2, -OH, =O, or-O-C(O)-R 5 ;

1 is 0, 1, or 2 ;

n is 1 or 2;

m is 1 or 2;

o is 0, 1, 2, 3, or 4;

p is 0, 1, 2, 3, or 4;

q is 0, 1, 2, or 3;

r is an integer from 0 to 5

R, R 1, and R 2 are selected from the group consisting of H, F, Cl, Br, I, CN, COOEt, OH, NO 2, NH 2, OR 5, wherein R 5 is C 1-8 alkyl, C 5-6 cycloalkyl, or C 2-8 alkenyl or R 2 is a 5 or 6 membered heterocycle,

and where any carbon of CH 2 m may be substituted by OR 7 where R 7 is C 1-18 alkyl or C 2-18 alkylene, or

where R 8 is C 1-18 alkyl or C 2-18 alkylene, or a pharmaceutically acceptable salt or derivative thereof.

2. A compound of claim 1 , wherein 1=0, n=2.

3. A compound of claim 1 , wherein 1=0, n =2, m=L

4. A compound of claim 1 , wherein X is —NH—or —O—. A-is-

5. A compound of claim 4 , wherein 1=0, n =2, m =1, and p=l.

6. A compound of claim 1 , selected from the group consisting of, trans-3-hydroxy-4-[2-diphenylmethoxy)ethyl] -1- [(4-fluorophenyl)methyl] piperidine, trans-3-propionyl-4-[2-(diphenylmethoxy)ethyl] -1 -[(4-fluorophenyl)methyl] piperidine, 3-keto-4-[2-(diphenylmethoxy)ethyl] -1 -[(4-fluorophenyl)methyl] piperidine, and the pharmaceutically acceptable salts and derivatives thereof.

7. The compound of claim 1 having the structure:

wherein A is

and where X is selected from the group consisting of —NH—, —NR 4 —, and —0—;

R 4 is C 1-4 alkyl, NH 2, C 1-4 hydroxyalkyl, halogenated C 1-4 alkyl, C 2-4 alkenyl, C 2-4 hydroxyalkenyl, halogenated C 2-4 alkenyl, C 2-4 and alkynyl, and C 2-4 halogenated alkynyl;

Y is —H, -NH 2, —OH, =O, or—O—C(o)-R 5 ;

wherein R 5 is C 1-8 alkyl, C 5-6 cycloalkyl, or C 2-8 alkenyl or R 5 is a 5 or 6 membered heterocycle;

m is 1 or 2;

p is 0, 1, 2, 3, or 4;

R1 is selected from the group consisting of H, F, Cl, Br, I, CN, COOEt, OH, NO 2, NH 2, OR 5, wherein R 5 is C 1-8 alkyl, C 5-6 cycloalkyl, or C 2-8 alkenyl or R 2 is a 5 or 6 membered heterocycle,

and where any carbon of CH 2 m may be substituted

by OR 7 where R 7 is C 1-18 alkyl or C 2-18 alkylene, or

where R 8 is C 1-18 alkyl or C 2-18 alkylene,

or a pharmaceutically acceptable salt or derivative thereof.

8. A compound of claim 1 , selected from the group consisting of:

and pharmaceutically acceptable salts and derivatives thereof.

9. The compound of claim 1 , having the structure:

and pharmaceutically acceptable salts and derivatives thereof.

10. A compound exhibiting CNS activity in mammalian species, having the formula:

wherein A is

and where X is selected from the group consisting of —NH—, —NR 4 —, and —0—; R 4 is C 1-4 alkyl, NH 2, C 1-4 hydroxyalkyl, halogenated C 1-4 alkyl, C 2-4 alkenyl, C 2-4 hydroxyalkenyl, halogenated C 2-4 alkenyl, C 2-4 and alkynyl, and C 2-4 halogenated alkynyl; Y is —OH, OR 9, NH 2, or NHR 9 wherein R 9 is wherein R 10 is C 6-20 alkyl,

o is 0, 1, 2, 3, or 4; R, R 1 and R 2 are selected from the group consisting of H, F, Cl, Br, I, CN, COOEt, OH, NO 2, NH 2, OR 5; wherein R 5 is C 1-8 alkyl, C 5-6 cycloalkyl, or C 2-8 alkenyl or R 2 is a 5 or 6 membered heterocycle; p is individually 0, 1, or 2, q is 0, 1, 2, or 3 wherein at least one R 2 is an electron withdrawing group, and pharmaceutically acceptable salts and derivatives thereof.

11. A compound having the following formula:

Assignments (2)
CONFIRMATORY LICENSE Recorded May 23, 2019
From: WAYNE STATE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 049264/0019 →
CONFIRMATORY LICENSE Recorded Apr 24, 2017
From: WAYNE STATE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 042320/0848 →
Continuity (3)
Continuation 1031179600
Provisional Application 6021292100 · Jun 20, 2000
Related Publication 20050154021A1 · Jul 14, 2005