IP Library Granted Patent US 8,481,534
Granted Patent B2
US 8,481,534 · App. 13/001,359 · Granted Jul 9, 2013

5- and 6-membered heterocyclic compounds

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Quick Facts
Patent No.
US 8,481,534
App. No.
13/001,359
Granted
Jul 9, 2013
Kind
B2
Abstract

5- and 6-membered heterocyclic compounds which are inhibitors of phosphodiesterase 10 are described as are processes, pharmaceutical compositions, pharmaceutical preparations and pharmaceutical use of the compounds in the treatment of mammals, including human(s) for central nervous system (CNS) disorders and other disorders which may affect CNS function. Also described is the treatment of neurological, neurodegenerative and psychiatric disorders including but not limited to those comprising cognitive deficits or schizophrenic symptoms.

Claims (27)

1. A compound of Formula (I)

or pharmaceutically acceptable salt thereof,

wherein:

HET is a heterocyclic ring having formula A7, A8, A10, A16, A17, A29 or A30

and the left most radical is connected to the X group;

X is optionally substituted heterocycloalkyl, optionally substituted aryl or optionally substituted heteroaryl;

Y is —CH 2 O— or —OCH 2 — with the rightmost radical of the Y group connected to the Z substituent;

Z is optionally substituted heteroaryl;

R 1a is hydrogen;

each R 2 is independently hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted cycloalkylalkyl or optionally substituted alkoxyalkyl, with the proviso that at least one R 2 is hydrogen;

R 3 and R 4 are independently hydrogen, C 1 -C 4 alkyl, —CF 3 or optionally substituted cycloalkyl, with the proviso that at least one R 3 or R 4 group must be hydrogen; and

R 7 is hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted cycloalkylalkyl or optionally substituted alkoxyalkyl.

2. The compound claim 1 , wherein Y is —CH 2 O— with the right most radical connected to the Z substituent, or a pharmaceutically acceptable salt thereof.

3. The compound of claim 1 , wherein Y is —OCH 2 — with the right most radical connected to the Z substituent, or a pharmaceutically acceptable salt thereof.

4. The compound of claim 1 , wherein Z is an optionally substituted heteroaryl having only 6 ring atoms or an optionally substituted heterobicyclic ring system, or a pharmaceutically acceptable salt thereof.

5. The compound of claim 1 , wherein Z is an optionally substituted heteroaryl having only 6 ring atoms selected from C and N provided the total number of ring nitrogens is less than or equal to two; said ring is optionally substituted with up to 2 substituents independently selected from the group consisting of C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkyloxy, C 4 -C 7 cycloalkylalkyl, cycloalkylalkoxy, halogen, alkylsulfonyl, cyano and nitro,

or a pharmaceutically acceptable salt thereof.

6. The compound of claim 1 , wherein Z is benzimidazolyl, quinolinyl, tetrahydroquinolyl, imidazo[1,2-a]pyridin-2-yl, tetrahydroisoquinolyl, 5-methylpyridin-2-yl, 3,5-dimethylpyridin-2-yl, 6-fluoroquinolyl or isoquinolinyl substituted with up to 3 substituents independently selected from the group consisting of C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 3 -C 6 cycloalkyl, C 3 -C 6 cycloalkyloxy, C 4 -C 7 cycloalkylalkyl, cycloalkylalkoxy, halogen, alkylsulfonyl, cyano and nitro,

or a pharmaceutically acceptable salt thereof.

7. The compound of claim 1 , wherein the Z substituent is unsubstituted, or a pharmaceutically acceptable salt thereof.

8. The compound of claim 1 , wherein X is a heterocycloalkyl having Formula B1-B16

wherein R 6 is hydrogen, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl or C 4 -C 7 cycloalkylalkyl,

or a pharmaceutically acceptable salt thereof.

9. The compound of claim 1 , wherein X is an optionally substituted heteroaryl, or a pharmaceutically acceptable salt thereof.

10. The compound of claim 1 , wherein X is phenyl, restricted phenyl or pyridinyl, or a pharmaceutically acceptable salt thereof.

11. The compound of claim 1 , wherein X is benzo[d]oxazoyl, benzo[c][1,2,5]oxadiazyl, benzo[c][1,2,5]thiadiazolyl, benzo[d]isoxazolyl, 1H-benzo[d]imidazoyl, benzo[d]thiazoyl, benzo[c]isothiazolyl, benzo[d]isothiazolyl, benzo[c]isoxazolyl, imidazo[1,2-a]pyridinyl or imidazo[1,5-a]pyridinyl, or a pharmaceutically acceptable salt thereof.

12. A pharmaceutical composition comprising: (i) the compound of any of claims 1 - 11 , or a pharmaceutically acceptable salt thereof; and (ii) a pharmaceutically acceptable carrier or excipient.

Assignments (3)
SECURITY INTEREST Recorded Jul 5, 2016
From: FORUM PHARMACEUTICALS INC.
To: FMR LLC
Reel/Frame 039254/0828 →
CHANGE OF NAME Recorded Oct 8, 2014
From: ENVIVO PHARMACEUTICALS, INC.
To: FORUM PHARMACEUTICALS INC.
Reel/Frame 033918/0197 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 5, 2011
From: RIPKA, AMY; SHAPIRO, GIDEON; CHESWORTH, RICHARD
To: ENVIVO PHARMACEUTICALS, INC.
Reel/Frame 026075/0075 →