IP Library Granted Patent US 9,334,268
Granted Patent B2
US 9,334,268 · App. 14/692,968 · Granted May 10, 2016

4-amino-imidazoquinoline compounds

Inventors: Sabine Hoves (Schlossbergstrasse, DE); Bernd Kuhn (Reinach, CH); Fabienne Ricklin (Hombourg, FR); Stephan Roever (Inzlingen, DE)
Assignee: HOFFMAN-LA ROCHE INC.
C07D471/04A61K31/4188A61K31/437
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Quick Facts
Patent No.
US 9,334,268
App. No.
14/692,968
Granted
May 10, 2016
Kind
B2
Abstract

This invention relates to novel 4-amino-imidazoquinoline compounds of the formula wherein R 1 to R 4 are as defined in the description and in the claims, as well as pharmaceutically acceptable salts thereof. These compounds are TLR agonists and may therefore be useful as medicaments for the treatment of diseases such as cancer or infectious diseases.

Claims (49)

1. A compound of formula I

wherein

R 1 is C 1-7 -alkyl or C 1-7 -alkoxy-C 1-7 -alkyl;

R 2 is selected from the group consisting of hydrogen, halogen, hydroxyl, hydroxy-C 1-7 -alkyl, alkoxy-C 1-7 -alkyl, carboxyl, carboxyl-C 1-7 -alkyl, carboxyl-C 2-7 -alkenyl, aminocarbonyl-C 1-7 -alkyl, aminocarbonyl-C 2-7 -alkenyl, C 1-7 -alkylamino-carbonyl-C 1-7 -alkyl, C 1-7 -alkylamino-carbonyl-C 2-7 -alkenyl, C 1-7 -alkoxycarbonyl-C 1-7 -alkyl, C 1-7 -alkoxycarbonyl-C 2-7 -alkenyl, C 1-7 -alkyl-sulfonyl-C 1-7 -alkyl, sulfamoyl-C 1-7 -alkyl, C 1-7 -alkyl-sulfamoyl-C 1-7 -alkyl,

phenyl, said phenyl being unsubstituted or substituted with one, two or three groups selected from the group consisting of C 1-7 -alkyl, C 1-7 -cycloalkyl, halogen, halogen-C 1-7 -alkyl, halogen-C 1-7 -alkoxy, hydroxy, hydroxy-C 1-7 -alkyl, C 1-7 -alkoxy, cyano, carboxyl, C 1-7 -alkoxycarbonyl, C 1-7 -alkoxycarbonyl-C 1-7 -alkyl, C 1-7 -alkylsulfonyl, hydroxy-C 1-7 -alkylsulfonyl, C 1-7 -alkoxy-C 1-7 -alkylsulfonyl, carboxyl-C 1-7 -alkylsulfonyl, C 1-7 -alkoxy-carbonyl-C 1-7 -alkylsulfonyl, amino, C 1-7 -alkylamino, di-C 1-7 -alkylamino and nitro, and

phenoxy, said phenoxy group being unsubstituted or substituted with one, two or three groups selected from the group consisting of C 1-7 -alkyl, C 1-7 -cycloalkyl, halogen, halogen-C 1-7 -alkyl, halogen-C 1-7 -alkoxy, hydroxy, hydroxy-C 1-7 -alkyl, C 1-7 -alkoxy, cyano, carboxyl, C 1-7 -alkoxycarbonyl, C 1-7 -alkoxycarbonyl-C 1-7 -alkyl, C 1-7 -alkyl-sulfonyl, hydroxy-C 1-7 -alkylsulfonyl, C 1-7 -alkoxy-C 1-7 -alkylsulfonyl, carboxyl-C 1-7 -alkylsulfonyl, C 1-7 -alkoxy-carbonyl-C 1-7 -alkylsulfonyl, amino, C 1-7 -alkylamino, di-C 1-7 -alkylamino and nitro;

R 3 is hydrogen or halogen;

R 4 is selected from the group consisting of

—O—(CH 2 ) m —NHR 5 , and

—O—(CO)—(CH 2 ) n —NHR 6 ,

wherein

m is selected from 1, 2 or 3,

n is selected from 1 or 2,

R 5 is selected from the group consisting of hydrogen, hydroxy-C 1-7 -alkyl, amino-C 1-7 -alkyl, C 1-7 -alkylcarbonyl, phenylcarbonyl, heteroarylcarbonyl, carboxyl, carboxyl-C 1-7 -alkyl and C 1-7 -alkoxycarbonyl-amino-C 1-7 -alkyl-carbonyl, and

R 6 is selected from the group consisting of hydrogen, hydroxy-C 1-7 -alkyl, amino-C 1-7 -alkyl, C 1-7 -alkylcarbonyl, phenylcarbonyl, heteroarylcarbonyl, carboxyl, carboxyl-C 1-7 -alkyl and C 1-7 -alkoxycarbonyl-amino-C 1-7 -alkyl-carbonyl,

or a pharmaceutically acceptable salt thereof.

2. A compound of formula I according to claim 1 , wherein R 1 is C 1-7 -alkoxy-C 1-7 -alkyl.

3. A compound of formula I according to claim 1 , wherein R 1 is ethoxyethyl.

4. A compound of formula I according to claim 1 , wherein R 3 is hydrogen.

5. A compound of formula I according to claim 1 , wherein R 4 is —O—(CH 2 ) m —NHR 5 and wherein m is selected from 1, 2 or 3 and wherein R 5 is selected from the group consisting of hydrogen, hydroxy-C 1-7 -alkyl, amino-C 1-7 -alkyl, C 1-7 -alkylcarbonyl, phenylcarbonyl, heteroarylcarbonyl, carboxyl, carboxyl-C 1-7 -alkyl and C 1-7 -alkoxycarbonyl-amino-C 1-7 -alkyl-carbonyl.

6. A compound of formula I according to claim 5 , wherein m is 2.

7. A compound of formula I according to claim 5 , wherein R 5 is selected from the group consisting of hydrogen, hydroxy-C 1-7 -alkyl, C 1-7 -alkylcarbonyl, heteroarylcarbonyl and C 1-7 -alkoxycarbonyl-amino-C 1-7 -alkyl-carbonyl.

8. A compound of formula I according to claim 5 , wherein R 5 is hydrogen.

9. A compound of formula I according to claim 1 , wherein R 4 is —O—(CO)—(CH 2 ) n —NHR 6 and wherein n is selected from 1 or 2 and wherein R 6 is selected from the group consisting of hydrogen, hydroxy-C 1-7 -alkyl, amino-C 1-7 -alkyl, C 1-7 -alkylcarbonyl, phenylcarbonyl, heteroarylcarbonyl, carboxyl, carboxyl-C 1-7 -alkyl and C 1-7 -alkoxycarbonyl-amino-C 1-7 -alkyl-carbonyl.

10. A compound of formula I according to claim 9 , wherein n is 1.

11. A compound of formula I according to claim 9 , wherein R 6 is hydrogen.

12. A compound of formula I according to claim 1 , wherein R 2 is selected from the group consisting of hydrogen, halogen, hydroxyl, hydroxy-C 1-7 -alkyl, alkoxy-C 1-7 -alkyl, carboxyl, carboxyl-C 1-7 -alkyl, carboxyl-C 2-7 -alkenyl, aminocarbonyl-C 1-7 -alkyl, aminocarbonyl-C 2-7 -alkenyl, C 1-7 -alkylamino-carbonyl-C 1-7 -alkyl, C 1-7 -alkylamino-carbonyl-C 2-7 -alkenyl, C 1-7 -alkoxycarbonyl-C 1-7 -alkyl, C 1-7 -alkoxycarbonyl-C 2-7 -alkenyl, C 1-7 -alkyl-sulfonyl-C 1-7 -alkyl, sulfamoyl-C 1-7 -alkyl and C 1-7 -alkyl-sulfamoyl-C 1-7 -alkyl.

13. A compound of formula I according to claim 1 , wherein R 2 is selected from the group consisting of hydrogen, halogen, C 1-7 -alkoxycarbonyl-C 1-7 -alkyl and C 1-7 -alkoxycarbonyl-C 2-7 -alkenyl.

14. A compound of formula I according to claim 1 , wherein R 2 is hydrogen.

15. A compound of formula I according to claim 1 , selected from the group consisting of

1-(2-(2-aminoethoxy)-2-methylpropyl)-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-4-amine,

1-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-yl 2-aminoacetate,

N-(2-(1-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-yloxy)ethyl)nicotinamide,

N-(2-(1-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-yloxy)ethyl)acetamide,

3-(2-(1-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-yloxy)ethylamino)propan-1-ol,

tert-butyl 6-(2-(1-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-yloxy)ethylamino)-6-oxohexylcarbamate,

ethyl (E)-3-[4-amino-1-[2-(2-aminoethoxy)-2-methylpropyl]-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-7-yl]prop-2-enoate,

ethyl 3-(4-amino-1-(2-(2-aminoethoxy)-2-methylpropyl)-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-7-yl)propanoate,

ethyl 3-(4-amino-1-(2-(2-aminoacetoxy)-2-methylpropyl)-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-7-yl)propanoate,

1-(2-(2-aminoethoxy)-2-methylpropyl)-2-pentyl-1H-imidazo[4,5-c]quinolin-4-amine, and

1-(2-(2-aminoethoxy)-2-methylpropyl)-7-bromo-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-4-amine, or a pharmaceutically acceptable salt thereof.

16. A compound of formula I according to claim 1 , which is 1-(2-(2-aminoethoxy)-2-methylpropyl)-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-4-amine, or a pharmaceutically acceptable salt thereof.

17. A compound of formula I which is 1-(4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-yl 2-aminoacetate, or a pharmaceutically acceptable salt thereof.

18. A compound of formula I according to claim 1 , or a pharmaceutically acceptable salt thereof, for use as medicament.

19. A pharmaceutical composition comprising a compound of formula I according to claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier and/or adjuvant.

20. A pharmaceutical composition comprising a compound of formula I according to claim 16 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier and/or adjuvant.

21. A pharmaceutical composition comprising a compound of formula I according to claim 17 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier and/or adjuvant.

22. A compound of formula I which is ethyl 3-(4-amino-1-(2-(2-aminoethoxy)-2-methylpropyl)-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-7-yl)propanoate, or a pharmaceutically acceptable salt thereof.

23. A pharmaceutical composition comprising a compound of formula I according to claim 22 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier and/or adjuvant.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2015
From: KUHN, BERND; RICKLIN, FABIENNE; ROEVER, STEPHAN
To: F. HOFFMANN-LA ROCHE AG
Reel/Frame 035472/0612 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2015
From: HOVES, SABINE
To: ROCHE DIAGNOSTICS GMBH
Reel/Frame 035473/0239 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2015
From: ROCHE DIAGNOSTICS GMBH
To: F. HOFFMANN-LA ROCHE AG
Reel/Frame 035473/0630 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2015
From: F. HOFFMANN-LA ROCHE AG
To: HOFFMANN-LA ROCHE INC.
Reel/Frame 035473/0742 →
Priority Claims (1)
EP 14165349 · Apr 22, 2014 · regional
Continuity (1)
Related Publication 20150299194A1 · Oct 22, 2015