IP Library Granted Patent US 8,697,873
Granted Patent B2
US 8,697,873 · App. 10/599,159 · Granted Apr 15, 2014

Amide substituted imidazopyridines, imidazoquinolines, and imidazonaphthyridines

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Quick Facts
Patent No.
US 8,697,873
App. No.
10/599,159
Granted
Apr 15, 2014
Kind
B2
Abstract

Imidazopyridine, imidazoquinoline, and imidazonaphthyridine compounds having an amide substituent at the 1-position, pharmaceutical compositions containing the compounds, intermediates, and methods of making and methods of use of these compounds as immunomodulators, for modulating cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.

Claims (100)

1. A compound of the formula (II):

wherein:

R 1 is selected from the group consisting of:

X′ is selected from the group consisting of —CH(R 9 )—, —CH(R 9 )-alkylene-, and —CH(R 9 )-alkenylene-;

X″ is selected from the group consisting of —CH(R 9 )—, —CH(R 9 )-alkylene-, and —CH(R 9 )— alkenylene-; wherein the alkylene and alkenylene are optionally interrupted with one or more —O— groups;

R 1 ′ and R 1 ″ are both

hydrogen;

A′ is selected from the group consisting of —O—, —C(O)—, —CH 2 —, —S(O) 0-2 —, and —N(Q-R 4 )—;

a and b are independently integers from 1 to 6 with the proviso that a+b is ≦7;

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 a groups, or a fused 6-membered saturated ring that is unsubstituted or substituted by one or more R c groups;

R a is selected from the group consisting of:

halogen,

alkyl,

haloalkyl,

alkoxy, and

—N(R 9 ) 2 ;

R c is selected from the group consisting of:

halogen,

hydroxy,

alkyl,

alkenyl,

haloalkyl,

alkoxy,

alkylthio, and

—N(R 9 ) 2 ;

R 2 is selected from the group consisting of hydrogen, alkyl, alkoxyalkyl, and hydroxyalkyl;

R 4 is selected from the group consisting of hydrogen, alkyl, and aryl;

R 6 is selected from the group consisting of ═O and ═S;

R 8 is selected from the group consisting of hydrogen, alkyl, alkoxyalkylenyl, and arylalkylenyl;

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

Q is selected from the group consisting of a bond, —C(R 6 )—, —C(R 6 )—C(R 6 )—, —S(O) 2 —, —C(R 6 )—N(R 8 )—W—, —S(O) 2 —N(R 8 )—, —C(R 6 )—O—, and —C(R 6 )—N(OR 9 )—; and

W is selected from the group consisting of a bond, —C(O)—, and —S(O) 2 —;

or a pharmaceutically acceptable salt thereof.

2. A compound of the formula (IV):

wherein:

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

X′ is selected from the group consisting of —CH(R 9 )—, —CH(R 9 )-alkylene-, and —CH(R 9 )— alkenylene-;

X″ is selected from the group consisting of —CH(R 9 )—, —CH(R 9 )-alkylene-, and —CH(R 9 )— alkenylene-; wherein the alkylene and alkenylene are optionally interrupted with one or more —O— groups;

R 1 ′ and R 1 ″ are both

hydrogen;

A′ is selected from the group consisting of —O—, —C(O)—, —CH 2 —, —S(O) 0-2 —, and —N(Q-R 4 )—;

a and b are independently integers from 1 to 6 with the proviso that a+b is ≦7;

R a is selected from the group consisting of:

halogen,

alkyl,

haloalkyl,

alkoxy, and

—N(R 9 ) 2

n is an integer from 0 to 4;

R 2 is selected from the group consisting of hydrogen, alkyl, alkoxyalkyl, and hydroxyalkyl;

R 4 is selected from the group consisting of hydrogen, alkyl, and aryl;

R 6 is selected from the group consisting of ═O and ═S;

R 8 is selected from the group consisting of hydrogen, alkyl, alkoxyalkylenyl, and arylalkylenyl;

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

Q is selected from the group consisting of a bond, —C(R 6 )—, —C(R 6 )—C(R 6 )—, —S(O) 2 —, —C(R 6 )—N(R 8 )—W—, —S(O 2 —N(R 8 )—, —C(R 6 )—O—, and —C(R 6 )—N(OR 9 )—; and

W is selected from the group consisting of a bond, —C(O)—, and —S(O) 2 —;

or a pharmaceutically acceptable salt thereof.

3. The compound or salt of claim 1 wherein the compound is of the following formula (V):

wherein:

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

X′ is selected from the group consisting of —CH(R 9 )—, —CH(R 9 )-alkylene-, and —CH(R 9 )— alkenylene-;

X″ is selected from the group consisting of —CH(R 9 )—, —CH(R 9 )-alkylene-, and —CH(R 9 )— alkenylene-; wherein the alkylene and alkenylene are optionally interrupted with one or more —O-groups;

R 1 ′ and R 1 ″ are both

hydrogen;

A′ is selected from the group consisting of —O—, —C(O)—, —CH 2 —, —S(O) 0-2 —, and —N(Q-R 4 )—;

a and b are independently integers from 1 to 6 with the proviso that a+b is ≦7;

R c is selected from the group consisting of:

halogen,

hydroxy,

alkyl,

alkenyl,

haloalkyl,

alkoxy,

alkylthio, and

—N(R 9 ) 2 ;

n is an integer from 0 to 4;

R 2 is selected from the group consisting of hydrogen, alkyl, alkoxyalkyl, and hydroxyalkyl;

R 4 is selected from the group consisting of hydrogen, alkyl, and aryl;

R 6 is selected from the group consisting of ═O and ═S;

R 8 is selected from the group consisting of hydrogen, alkyl, alkoxyalkylenyl, and arylalkylenyl;

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

Q is selected from the group consisting of a bond, —C(R 6 )—, —C(R 6 )—C(R 6 )—, —S(O) 2 —, —C(R 6 )—N(R 8 )—W—, —S(O) 2 —N(R 8 )—, —C(R 6 )—O—, and —C(R 6 )—N(OR 9 )—; and

W is selected from the group consisting of a bond, —C(O)—, and —S(O) 2 ;

or a pharmaceutically acceptable salt thereof.

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

5. The compound or salt of claim 1 wherein X′ is —CH 2 —C 0-10 alkylene- or X″ is —CH 2 —C 0-10 alkylene- or —CH 2 —C 1-4 alkylene-O—C 1-4 alkylene-.

6. The compound or salt of claim 5 wherein X′ is —(CH 2 ) 1-5 —, —CH 2 C(CH 3 ) 2 —, or —CH 2 C(CH 3 ) 2 CH 2 —; or X″ is —(CH 2 ) 1-5 —, —CH 2 C(CH 3 ) 2 —, —CH 2 C(CH 3 ) 2 CH 2 —, or —(CH 2 ) 3 —O—CH 2 —.

7. The compound or salt of claim 1 wherein R 2 is hydrogen, C 1-4 alkyl, hydroxy C 1-4 alkylenyl, or C 1-4 alkyl-O—C 14 alkylenyl.

8. A pharmaceutical composition comprising a therapeutically effective amount of a compound or salt of claim 1 and a pharmaceutically acceptable carrier.

9. The compound or salt of claim 2 wherein R 1-1 is

A′ is —O—, and a and b are each 2.

10. The compound or salt of claim 2 wherein X′ is —CH 2 —C 0-10 alkylene- or X″ is —CH 2 —C 0-10 alkylene- or —CH 2 —C 1-4 -alkylene-O—C 1-4 alkylene-.

11. The compound or salt of claim 10 wherein X′ is —(CH 2 ) 1-5 —, —CH 2 C(CH 3 ) 2 —, or —CH 2 C(CH 3 ) 2 CH 2 —; or X″ is —(CH 2 ) 1-5 —, —CH 2 C(CH 3 ) 2 —, —CH 2 C(CH 3 ) 2 CH 2 —, or —(CH 2 ) 3 —CH 2 —.

12. The compound or salt of claim 2 wherein R 2 is hydrogen, C 1-4 alkyl, hydroxy C 1-4 alkylenyl, or C 1-4 alkyl-O—C 1-4 alkylenyl.

13. The compound or salt of claim 3 wherein R 1-1 is

A′ is —O—, and a and b are each 2.

14. The compound or salt of claim 3 wherein X is —CH 2 —C 0-10 alkylene- or X″ is —CH 2 —C 0-10 alkylene- or —CH 2 —C 1-4 alkylene-O—C 1-4 alkylene-.

15. The compound or salt of claim 3 wherein R 2 is hydrogen, C 1-4 alkyl, hydroxyC 1-4 alkylenyl, or C 1-4 alkyl-O—C 1-4 alkylenyl.

16. A pharmaceutical composition comprising a therapeutically effective amount of a compound or salt of claim 2 and a pharmaceutically acceptable carrier.

17. A pharmaceutical composition comprising a therapeutically effective amount of a compound or salt of claim 3 and a pharmaceutically acceptable carrier.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2024
From: 3M INNOVATIVE PROPERTIES COMPANY
To: SOLVENTUM INTELLECTUAL PROPERTIES COMPANY
Reel/Frame 066433/0049 →
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 Sep 21, 2006
From: KREPSKI, LARRY R.; DELLARIA, JOSEPH F. JR.,; DUFFY, DANIEL E.; AMOS, DAVID T.; ZIMMERMANN, BERNHARD M.; MOSER, WILLIAM H.
To: 3M INNOVATIVE PROPERTIES COMPANY
Reel/Frame 018295/0187 →