IP Library Granted Patent US 8,691,837
Granted Patent B2
US 8,691,837 · App. 10/595,959 · Granted Apr 8, 2014

Substituted imidazo ring systems and methods

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 8,691,837
App. No.
10/595,959
Granted
Apr 8, 2014
Kind
B2
Abstract

Imidazo ring systems substituted at the 1-position, pharmaceutical compositions containing the compounds, intermediates, methods of making the compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

Claims (135)

1. A compound of the Formula (I-1):

wherein:

X is alkylene;

Z is —C(O)—;

R 1-1 is selected from the group consisting of:

hydrogen,

alkyl,

phenyl,

—N(CH 3 )(OCH 3 ), and

alkyl or phenyl, substituted by one or more substituents selected from the group consisting of:

halogen,

alkoxy,

dialkylamino,

alkylthio,

haloalkyl,

haloalkoxy, and

alkyl; and

R 2 is selected from the group consisting of:

hydrogen,

alkyl,

hydroxyalkyl, and

alkyloxyalkyl;

R A and R B are taken together to form either a fused aryl ring that is unsubstituted or substituted by one or more R groups, or a fused 5 to 7 membered saturated ring that is unsubstituted or substituted by one or more R a groups;

R is selected from the group consisting of:

fluoro,

alkyl,

haloalkyl,

alkoxy, and

—N(R 9 ) 2 ; and

R a is selected from the group consisting of:

halogen,

hydroxy,

alkyl,

alkenyl,

haloalkyl,

alkoxy,

alkylthio, and

—N(R 9 ) 2 ; and R9 is selected from the group consisting of hydrogen and alkyl;

or a pharmaceutically acceptable salt thereof.

2. A compound of the Formula (I-2):

wherein:

X is alkylene;

n is an integer from 0 to 4;

Z is —C(O)—;

R 1-1 is selected from the group consisting of:

hydrogen,

alkyl,

phenyl,

—N(CH 3 )(OCH 3 ), and

alkyl or phenyl, substituted by one or more substituents selected from the group consisting of:

halogen,

alkoxy,

dialkylamino,

alkylthio,

haloalkyl,

haloalkoxy, and

alkyl;

R is selected from the group consisting of:

fluoro,

alkyl,

haloalkyl,

alkoxy, and

—N(R 9 ) 2 ;

R 2 is selected from the group consisting of:

hydrogen,

alkyl,

hydroxyalkyl, and

alkyloxyalkyl; and

R 9 is selected from the group consisting of hydrogen and alkyl;

or a pharmaceutically acceptable salt thereof.

3. A compound of the Formula (Ia):

wherein:

X is alkylene;

n is an integer from 0 to 4;

R 1-1 is selected from the group consisting of:

hydrogen,

alkyl,

phenyl,

—N(CH 3 )(OCH 3 ), and

alkyl or phenyl, substituted by one or more substituents selected from the group consisting of:

halogen,

alkoxy,

dialkylamino,

alkylthio,

haloalkyl,

haloalkoxy, and

alkyl;

R is selected from the group consisting of:

fluoro,

alkyl,

haloalkyl,

alkoxy, and

—N(R 9 ) 2 ;

R 2 is selected from the group consisting of:

hydrogen,

alkyl,

hydroxyalkyl, and

alkyloxyalkyl; and

R 9 is selected from the group consisting of hydrogen and alkyl;

or a pharmaceutically acceptable salt thereof.

4. A compound of the Formula (Ie):

wherein:

X is alkylene;

n is an integer from 0 to 4;

R is selected from the group consisting of:

fluoro,

alkyl,

alkoxy,

haloalkyl, and

—N(R 9 ) 2 ;

R 2 is selected from the group consisting of:

hydrogen,

alkyl,

hydroxyalkyl, and

alkyloxyalkyl; and

R 9 is selected from the group consisting of hydrogen and alkyl;

or a pharmaceutically acceptable salt thereof.

5. The compound or salt of claim 2 wherein n is 0.

6. The compound or salt of claim 1 wherein R 1-1 is selected from the group consisting of phenyl, alkyl, and —N(CH 3 )OCH 3 .

7. The compound or salt of claim 1 wherein X is C 1-6 alkylene.

8. The compound or salt of claim 7 wherein X is selected from the group consisting of —(CH 2 ) 1-6 —, —CH 2 —C(CH 3 ) 2 —, and —CH 2 —C(CH 3 ) 2 —CH 2 —.

9. The compound or salt of claim 1 wherein R 1-1 is selected from the group consisting of alkyl and phenyl.

10. The compound or salt of claim 1 wherein R 1-1 is selected from the group consisting of methyl, ethyl, n-propyl, isopropyl, cyclopropyl, n-butyl, sec-butyl, isobutyl, tent-butyl, n-pentyl, cyclopentyl, n-hexyl, cyclohexyl, phenyl, 4-chlorophenyl and 2,4-dichlorophenyl.

11. The compound or salt of claim 1 wherein R 2 is selected from the group consisting of hydrogen, hydroxymethyl, methyl, ethyl, n-propyl, n-butyl, ethoxymethyl, and 2-methoxyethyl.

12. A pharmaceutical composition comprising a therapeutically effective amount of a compound or salt of claim 1 in combination with a pharmaceutically acceptable carrier.

13. A method of inducing cytokine biosynthesis in an animal comprising administering an effective amount of a compound or salt of claim 1 to the animal wherein the cytokine is selected from INF and TNF.

14. The compound or salt of claim 2 wherein X is C 1-6 alkylene.

15. The compound or salt of claim 14 wherein X is selected from the group consisting of —(CH 2 ) 1-6 —, —CH 2 —C(CH 3 ) 2 —, and —CH 2 —C(CH 3 ) 2 —CH 2 —.

16. The compound or salt of claim 2 wherein R 1-1 is selected from the group consisting of alkyl and phenyl.

17. The compound or salt of claim 2 wherein R 1-1 is selected from the group consisting of methyl, ethyl, n-propyl, isopropyl, cyclopropyl, n-butyl, sec-butyl, isobutyl, tent-butyl, n-pentyl, cyclopentyl, n-hexyl, cyclohexyl, phenyl, 4-chlorophenyl and 2,4-dichlorophenyl.

18. The compound or salt of claim 2 wherein R 2 is selected from the group consisting of hydrogen, hydroxymethyl, methyl, ethyl, n-propyl, n-butyl, ethoxymethyl, and 2-methoxyethyl.

19. A pharmaceutical composition comprising a therapeutically effective amount of a compound or salt of claim 2 in combination with a pharmaceutically acceptable carrier.

20. A method of inducing cytokine biosynthesis in an animal comprising administering an effective amount of a compound or salt of claim 2 to the animal wherein the cytokine is selected from INF and TNF.

21. A pharmaceutical composition comprising a therapeutically effective amount of a compound or salt of claim 4 in combination with a pharmaceutically acceptable carrier.

22. A method of inducing cytokine biosynthesis in an animal comprising administering an effective amount of a compound or salt of claim 4 to the animal wherein the cytokine is selected from INF and TNF.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 22, 2011
From: COLEY PHARMACEUTICAL GROUP, INC.
To: 3M INNOVATIVE PROPERTIES COMPANY
Reel/Frame 025839/0772 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2007
From: 3M COMPANY; 3M INNOVATIVE PROPERTIES COMPANY
To: COLEY PHARMACEUTICAL GROUP, INC.
Reel/Frame 019945/0698 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 22, 2006
From: AMOS, DAVID T.; KREPSKI, LARRY R.; DELLARIA, JOSEPH F. JR.; DUFFY, DANIEL E.; RADMER, MATTHEW R.
To: 3M INNOVATIVE PROPERTIES COMPANY
Reel/Frame 017664/0194 →