IP Library Granted Patent US 8,148,399
Granted Patent B2
US 8,148,399 · App. 11/632,102 · Granted Apr 3, 2012

Macrocyclic inhibitors of hepatitis C virus

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Quick Facts
Patent No.
US 8,148,399
App. No.
11/632,102
Granted
Apr 3, 2012
Kind
B2
Abstract

Inhibitors of HCV replication of formula (I) and the N-oxides, salts, and stereoisomers, wherein each dashed line represents an optional double bond; X is N, CH and where X bears a double bond it is C; R 1 is —OR 7 , —NH—SO 2 R 8 ; R 2 is hydrogen, and where X is C or CH, R 2 may also be C 1-6 alkyl; R 3 is hydrogen, C 1-6 alkyl, C 3-7 cycloalkyl; R 4 is aryl or Het; n is 3, 4, 5, or 6; R 5 is halo, C 1-6 alkyl, hydroxy, C 1-6 alkoxy, phenyl, or Het; R 6 is C 1-6 alkoxy, or dimethylamino; R 7 is hydrogen; aryl; Het; C 3-7 cycloalkyl optionally substituted with C 1-6 alkyl; or C 1-6 alkyl optionally substituted with C 3-7 cycloalkyl, aryl or with Het; R 8 is aryl; Het; C 3-7 cycloalkyl optionally substituted with C 1-6 alkyl; or C 1-6 alkyl optionally substituted with C 3-7 cycloalkyl, aryl or with Het; aryl is phenyl optionally substituted with one, two or three substituents; Het is a 5 or 6 membered saturated, partially unsaturated or completely unsaturated heterocyclic ring containing 1 to 4 heteroatoms selected from nitrogen, oxygen and sulfur, and being optionally substituted with one, two or three substituents; pharmaceutical compositions containing compounds (I) and processes for preparing compounds (I). Bioavailable combinations of the inhibitors of HCV of formula (I) with ritonavir are also provided.

Claims (27)

1. A compound of the formula:

or a pharmaceutically acceptable salt thereof or a stereochemically isomeric form thereof or a pharmaceutically acceptable salt of the stereochemically isomeric form.

2. A compound of the formula:

or a pharmaceutically acceptable salt thereof.

3. The compound according to claim 2 in its pharmaceutically acceptable salt form.

4. The compound according to claim 3 wherein the pharmaceutically acceptable salt is an acid addition salt.

5. The compound according to claim 3 wherein the pharmaceutically acceptable salt is a base addition salt.

6. The compound according to claim 3 wherein the pharmaceutically acceptable salt is a hydrochloride acid addition salt.

7. The compound according to claim 3 wherein the pharmaceutically acceptable salt is a sodium addition salt.

8. The compound according to claim 2 , which is stereochemically pure.

9. The compound according to claim 1 wherein the compound is a powder.

10. A pharmaceutical composition comprising a therapeutically effective amount of the compound of claim 1 and a pharmaceutically acceptable carrier therefore.

11. A method of inhibiting HCV replication in a warm-blooded animal comprising administering to said animal in need thereof a therapeutically effective amount of a compound according to claim 1 .

12. The method according to claim 11 wherein the warm-blooded animal is human.

13. The method according to claim 11 wherein the compound has the formula

or a pharmaceutically acceptable salt thereof.

14. A process of preparing a compound of the formula

which comprises reacting under effective conditions a compound of formula 46

and cyclopropylsulfonamide.

15. The process according to claim 14 wherein the process comprises

(a) stirring at reflux under nitrogen for 2 hours, a solution of 560 mg (0.867 mmol) of compound no. 46 and 308 mg (1.90 mmol) of carbonyldiimidazole in 10 mL of dry tetrahydrofuran;

(b) cooling the reaction mixture obtainable from step a) to room temperature and adding 400 mg (3.301 mmol) of cyclopropylsulfonamide and 286 mg of DBU (1.881 mmol);

(c) heating the solution obtainable from step b) at 50° C. for 15 hours;

(d) cooling down the reaction mixture obtainable from step c) at room temperature and concentrating it under reduced pressure;

(e) partitioning the residue obtainable from step d) between CH 2 Cl 2 and HCl 1 N, washing the organic layer with brine, drying said organic layer with MgSO 4 , and evaporating said organic layer;

(f) purifying the organic layer obtainable from step e) by flash chromatography (gradient of EtOAc (0 to 25%) in CH 2 Cl 2 ) affording 314 mg of an off-white solid; and

(g) washing the off-white solid obtainable from step f) with water and then with isopropyl ether, and drying said off-white solid in a vacuum oven.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2015
From: JANSSEN R & D IRELAND
To: JANSSEN SCIENCES IRELAND UC
Reel/Frame 035496/0382 →
CHANGE OF NAME Recorded Apr 15, 2015
From: TIBOTEC PHARMACEUTICALS
To: JANSSEN R&D IRELAND
Reel/Frame 035439/0981 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2011
From: TIBOTEC BVBA
To: TIBOTEC PHARMACEUTICALS LTD.
Reel/Frame 025857/0828 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2007
From: SIMMEN, KENNETH; DE KOCK, HERMAN; RABOISSON, PIERRE; VENDEVILLE, SANDRINE; HU, LILI; TAHRI, ABDELLAH; SURLERAUX, DOMINIQUE
To: TIBOTEC BVBA
Reel/Frame 018790/0617 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2007
From: NILSSON, KARL; SAMUELSSON, BENGT; ROSENQUIST, ASA; IVANOV, VLADIMIR; PELCMAN, MICHAEL; BELFRAGE, ANNA; JOHANSSON, PER-OLA
To: MEDIVIR AB
Reel/Frame 018790/0636 →