IP Library Granted Patent US 8,658,666
Granted Patent B2
US 8,658,666 · App. 11/884,191 · Granted Feb 25, 2014

Substituted imidazoquinolines and imidazonaphthyridines

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Quick Facts
Patent No.
US 8,658,666
App. No.
11/884,191
Granted
Feb 25, 2014
Kind
B2
Abstract

Imidazoquinolines and imidazonaphthyridines with a substituent containing a functional group, e.g., an amide, sulfonamide, urea, or heterocyclyl group, at the 6, 7, 8, or 9-position, pharmaceutical compositions containing the compounds, intermediates, methods of making 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 (78)

1. A compound of the Formula II:

wherein:

R 3 is selected from the group consisting of:

-Z-Y-R 4 , and

-Z-R 5 ;

R is selected from the group consisting of alkyl, alkoxy, hydroxy, halogen, and trifluoromethyl;

n is 0 or 1;

R 1 is selected from the group consisting of alkyl, alkoxyalkylenyl, dihydroxyalkylenyl, hydroxyalkylenyl, and alkyl substituted by a group selected from the group consisting of —NH—C(O)-alkyl, —NH—S(O) 2 -alkyl, —NH—C(O)—NH-alkyl, tetrahydropyranyl, phenoxy, 1,1-dioxidoisothiazolidin-2-yl, and 2-oxo-pyrroldin-1-yl;:

R 2 is selected from the group consisting of hydrogen, alkyl, alkoxyalkylenyl, and hydroxyalkylenyl;

Z is selected from the group consisting of a bond, and alkylene;

Y is selected from the group consisting of:

—S(O) 0-2 —,

—S(O) 2 —N(R 8 )—,

—C(R 6 )—,

—N(R 8 )-Q-,

—C(R 6 )—N(R 8 )—, and

—O—C(R 6 )—N(R 8 )—,

R 4 is selected from the group consisting of hydrogen, alkyl, and heterocyclyl wherein the alkyl, and heterocyclyl groups can be unsubstituted or substituted by one or more substituents independently selected from the group consisting of alkyl, alkoxy, hydroxyalkyl, haloalkyl, haloalkoxy, halogen, hydroxy, amino, alkylamino, dialkylamino, and in the case of alkyl, and heterocyclyl, oxo;

R 5 is selected from the group consisting of:

R 6 is ═O;

R 7 is C 2-7 alkylene;

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

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

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

V is selected from the group consisting of —C(R 6 )—, —O—C(R 6 )—, —N(R 8 )—C(R 6 )—, and —S(O) 2 —;

W is a bond; and

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

with the proviso that when R 3 is -Z-Y-R 4 and Z is a bond, then Y is selected from the group consisting of —N(R 8 )-Q-, S(O) 0-2 , and —C(R 6 )— wherein Q is selected from the group consisting of —C(R 6 )—, S(O) 2 —, —C(R 6 )—N(R 8 )—W—; and

with the further proviso that when R 3 is -Z-R 5 , then Z is alkylene or alkenylene;

or a pharmaceutically acceptable salt thereof.

2. The compound or salt of claim 1 wherein n is 0.

3. The compound or salt of claim 1 wherein R 3 is -Z-Y-R 4 .

4. The compound or salt of claim 3 wherein Y is —N(R 8 )-Q-, and R 4 is alkyl, or heterocyclyl.

5. The compound or salt of claim 1 wherein Z is C 1-4 alkylene.

6. The compound or salt of claim 1 wherein R 3 is at the 7-position.

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

8. The compound or salt of claim 1 wherein R 1 is selected from the group consisting of 2-hydroxy-2-methylpropyl, 2-methylpropyl, propyl, ethyl, methyl, 2,3-dihydroxypropyl, 3-isopropoxypropyl, 2-phenoxyethyl, 4-[(methylsulfonyl)amino]butyl, 2-methyl-2-[(methylsulfonyl)amino]propyl, 2-(acetylamino)-2-methylpropyl, 2-{[(isopropylamino)carbonyl]amino}-2-methylpropyl, 4-{[(isopropylamino)carbonyl]amino}butyl, 4-(1,1-dioxidoisothiazolidin-2-yl)butyl, and tetrahydro-2H-pyran-4-ylmethyl.

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

10. The compound or salt of claim 4 wherein Q is —C(R 6 )—, —S(O) 2 —, or —C(R 6 )—N(R 8 )—.

11. The compound or salt of claim 1 wherein R 1 is selected from the group consisting of alkyl, hydroxyalkylenyl, alkoxyalkylenyl, and alkyl substituted by tetrahydropyranyl.

12. The compound or salt of claim 1 wherein R 1 is alkyl substituted by —NH—S(O) 2 -alkyl.

13. The compound or salt of claim 1 wherein R 1 is selected from the group consisting of 2-hydroxy-2-methylpropyl, 2-methylpropyl, 4-[(methylsulfonyl)amino]butyl, 2-methyl-2-[(methylsulfonyl)amino]propyl, tetrahydro-2H-pyran-4-ylmethyl, and 3-isopropoxypropyl.

14. The compound or salt of claim 11 wherein R 1 is selected from the group consisting of 2-hydroxy-2-methylpropyl, 2-methylpropyl, tetrahydro-2H-pyran-4-ylmethyl, and 3-isopropoxypropyl.

15. A compound selected from the group consisting of:

2-ethyl-7-[2-(methylsulfonyl)ethyl]-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-4-amine;

N-{3-[4-amino-2-ethyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-7-yl]propyl}methane sulfonamide;

N-{3-[4-amino-2-ethyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-7-yl]propyl}acetamide;

N-{3-[4-amino-2-ethyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-7-yl]propyl}-N′-isopropylurea;

3-[4-amino-2-ethyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-7-yl]-N,N-dimethylpropanamide;

or a pharmaceutically acceptable salt thereof.

16. A compound selected from the group consisting of:

3-[4-amino-2-ethyl-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]-1-(morpholin-4-yl)propan-1-one;

1-{4-amino-7-[2-(methylsulfonyl)ethyl]-1H-imidazo[4,5-c]quinolin-1-yl}-2-methylpropan-2-ol;

3-[4-amino-2-ethyl-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]-N,N-dimethylpropanamide;

1-{4-amino-2-(methoxymethyl)-7-[2-(methylsulfonyl)ethyl]-1H-imidazo[4,5-c]quinolin-1-yl}-2-methylpropan-2-ol;

1-{4-amino-2-(hydroxymethyl)-7-[2-(methylsulfonyl)ethyl]-1H-imidazo[4,5-c]quinolin-1-yl}-2-methylpropan-2-ol;

1-[4-amino-2-(methoxymethyl)-7-(3-morpholin-4-yl-3-oxopropyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-ol;

1-[4-amino-7-[3-(1,1-dioxidothiomorpholin-4-yl)-3-oxopropyl]-2-(methoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-ol;

3-[4-amino-1-(2-hydroxy-2-methylpropyl)-2-(methoxymethyl)-1H-imidazo[4,5-c]quinolin-7-yl]-N,N-dimethylpropanamide;

N-{3-[4-amino-1-(2-hydroxy-2-methylpropyl)-2-(methoxymethyl)-1H-imidazo[4,5-c]quinolin-7-yl]propyl}methanesulfonamide;

3-[4-amino-2-(hydroxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]-N,N-dimethylpropanamide;

1-[4-amino-2-(hydroxymethyl)-7-(3-morpholin-4-yl-3-oxopropyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-ol;

3-[4-amino-1-(2-hydroxy-2-methylpropyl)-2-(methoxymethyl)-1H-imidazo[4,5-c]quinolin-7-yl]propanamide;

1-[4-amino-7-[3-(1,1-dioxidothiomorpholin-4-yl)-3-oxopropyl]-2-(hydroxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-ol;

N-{3-[4-amino-1-(2-hydroxy-2-methylpropyl)-2-(methoxymethyl)-1H-imidazo[4,5-c]quinolin-7-yl]propyl}acetamide;

N-{3-[4-amino-2-(hydroxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]propyl}methanesulfonamide;

N-{2-[4-amino-2-ethyl-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]ethyl}methanesulfonamide;

1-[4-amino-2-(ethoxymethyl)-7-(3-morpholin-4-yl-3-oxopropyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-ol;

or a pharmaceutically acceptable salt thereof.

17. A compound selected from the group consisting of:

1-{3-[4-amino-2-(2-methoxyethyl)-8-(3-morpholin-4-yl-3-oxo-propyl)-1H-imidazo[4,5-c]quinolin-1-yl]propyl}pyrrolidin-2-one;

3-{4-amino-2-(2-methoxyethyl)-1-[3-(2-oxo-pyrrolidin-1-yl)propyl]-1H-imidazo[4,5-c]quinolin-8-yl}-N,N-dimethylpropanamide;

N-[4-amino-2-ethoxymethyl-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-yl]ethanesulfonamide;

or a pharmaceutically acceptable salt thereof.

18. The compound or salt of claim 4 wherein R 8 is hydrogen; Q is —C(O)—, —S(O) 2 —, or —C(O)—NH—; and R 4 is alkyl.

19. The compound or salt of claim 1 wherein R 3 is -Z-R 5 .

20. The compound or salt of claim 19 wherein Z is C 2-4 alkylene and R 5 is

wherein a and b are both 2.

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 Jun 18, 2008
From: 3M COMPANY & 3M INNOVATIVE PROPERTIES COMPANY
To: COLEY PHARMACEUTICAL GROUP, INC.
Reel/Frame 021111/0521 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 17, 2008
From: GERSTER, JOHN F.; MERRILL, BYRON A.; RICE, MICHAEL J.; HARALDSON, CHAD A.; WURST, JOSHUA A.; HEPPNER, PHILIP D.; KSHIRSAGAR, TUSHAR A.
To: 3M COMPANY & 3M INNOVATIVE PROPERTIES COMPANY
Reel/Frame 021107/0764 →