Granted Patent B2

US 7,759,348 · App. 12/036,685 · Granted Jul 20, 2010

Assignees: Xenon Pharmaceuticals Inc.; Novartis Pharma AG

Abstract

Claims (48)

1. A method of treating a skin disorder mediated by stearoyl-CoA desaturase (SCD) in a mammal selected from the group consisting of acne, rosacea, seborrheic skin, and a combination thereof, wherein the method comprises administering to the mammal in need thereof a therapeutically effective amount of a compound of formula (I):

wherein:

x and y are each independently 1;

W is —C(O)N(R 1 )—; —C(O)N[C(O)R 1a ]—, —N(R 1 )C(O)N(R 1 )— or —N(R 1 )C(O)—;

V is —C(O)—, —C(S)—, or —C(R 10 )H;

each R 1 is independently selected from the group consisting of hydrogen; C 1 -C 6 alkyl optionally substituted with one or more substituents selected from the group consisting of halo, methyl or trifluoromethyl; and C 2 -C 6 alkyl optionally substituted with one or more substituents selected from the group consisting of methoxy and hydroxyl;

R 1a is selected from the group consisting of hydrogen, C 1 -C 6 alkyl and cycloalkyl;

R 2 is selected from the group consisting of C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 2 -C 12 hydroxyalkyl, C 2 -C 12 hydroxyalkenyl, C 1 -C 12 alkoxy, C 2 -C 12 alkoxyalkyl, C 3 -C 12 cycloalkyl, C 4 -C 12 cycloalkylalkyl, aryl, C 7 -C 12 aralkyl, C 3 -C 12 heterocyclyl, C 3 -C 12 heterocyclylalkyl, C 1 -C 12 heteroaryl, and C 3 -C 12 heteroarylalkyl;

or R 2 is a multi-ring structure having 2 to 4 rings wherein the rings are independently selected from the group consisting of cycloalkyl, heterocyclyl, aryl and heteroaryl and where some or all of the rings may be fused to each other;

R 3 is selected from the group consisting of C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 2 -C 12 hydroxyalkyl, C 2 -C 12 hydroxyalkenyl, C 1 -C 12 alkoxy, C 2 -C 12 alkoxyalkyl, C 3 -C 12 cycloalkyl, C 4 -C 12 cycloalkylalkyl, aryl, C 7 -C 12 aralkyl, C 3 -C 12 heterocyclyl, C 3 -C 12 heterocyclylalkyl, C 1 -C 12 heteroaryl and C 3 -C 12 heteroarylalkyl;

or R 3 is a multi-ring structure having 2 to 4 rings wherein the rings are independently selected from the group consisting of cycloalkyl, heterocyclyl, aryl and heteroaryl and where some or all of the rings may be fused to each other;

R 4 and R 5 are each independently selected from hydrogen, fluoro, chloro, methyl, methoxy, trifluoromethyl, cyano, nitro or —N(R 12 ) 2 ;

R 6 , R 6a , R 7 , R 7a , R 8 , R 8a , R 9 , and R 9a are each independently selected from hydrogen or C 1 -C 3 alkyl;

or R 6 and R 6a together, or R 7 and R 7a together, or R 8 and R 8a together or R 9 and R 9a together are an oxo group, provided that when V is —C(O)—, R 7 and R 7a together, or R 8 and R 8a together, do not form an oxo group;

or one of R 6 , R 6a , R 7 , and R 7a together with one of R 8 , R 8a , R 9 and R 9a form an alkylene bridge;

R 10 is hydrogen or C 1 -C 3 alkyl; and

each R 12 is independently selected from hydrogen or C 1 -C 6 alkyl;

a stereoisomer, enantiomer or tautomer thereof, a pharmaceutically acceptable salt thereof, or a pharmaceutical composition thereof.

2. The method of claim 1 , wherein the mammal is a human.

3. The method of claim 1 , wherein the administering is by topical administration.

4. The method of claim 1 , wherein the pharmaceutical composition of the compound of formula (I) comprises a percutaneous penetration enhancer.

5. The method of claim 4 , wherein the percutaneous penetration enhancer is SEPA-9.

6. The method of claim 1 , wherein the skin disorder is rosacea.

7. The method of claim 1 , wherein the skin disorder is seborrheic skin.

8. The method of claim 1 ,

wherein

V is —C(O)— or —C(S)—;

W is selected from —C(O)N(R 1 )— and —N(R 1 )C(O)—;

R 2 is selected from the group consisting of C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 2 -C 12 hydroxyalkyl, C 2 -C 12 hydroxyalkenyl, C 1 -C 6 alkoxy, C 3 -C 12 alkoxyalkyl, C 3 -C 12 cycloalkyl, C 4 -C 2 cycloalkylalkyl, aryl, C 7 -C 12 aralkyl, C 3 -C 12 heterocyclyl, C 3 -C 12 heterocyclylalkyl, C 1 -C 12 heteroaryl and C 3 -C 12 heteroarylalkyl;

R 3 is phenyl optionally substituted by one or more substituents selected from the group consisting of halo, cyano, nitro, hydroxy, C 1 -C 6 alkyl, C 1 -C 6 trihaloalkyl, C 1 -C 6 trihaloalkoxy, C 1 -C 6 alkylsulfonyl, —N(R 11 ) 2 , —OC(O)R 11 , —C(O)OR 11 , —S(O) 2 N(R 11 ) 2 , cycloalkyl, heterocyclyl, heteroaryl and heteroarylcycloalkyl, provided that R 3 is not phenyl substituted with optionally substituted thienyl;

R 4 and R 5 are each independently selected from hydrogen, fluoro, chloro, methyl, methoxy and trifluoromethyl; and

R 6 , R 6a , R 7 , R 7a , R 8 , R 8a , R 9 , and R 9a are each independently selected from hydrogen or C 1 -C 3 alkyl.

9. The method of claim 1 ,

wherein

V is —C(O)—;

W is selected from —C(O)N(R 1 )— and —N(R 1 )C(O)—;

R 2 is selected from the group consisting of C 7 -C 12 alkyl, C 3 -C 12 alkenyl, C 7 -C 12 hydroxyalkyl, C 2 -C 12 alkoxyalkyl, C 3 -C 12 hydroxyalkenyl, C 3 -C 12 cycloalkyl, C 4 -C 12 cycloalkylalkyl, C 3 -C 9 aralkyl, C 3 -C 12 heterocyclylalkyl, and C 3 -C 12 heteroarylalkyl;

R 3 is selected from the group consisting of C 3 -C 12 alkyl, C 3 -C 12 alkenyl, C 3 -C 12 hydroxyalkyl, C 3 -C 12 hydroxyalkenyl, C 3 -C 12 alkoxy, C 3 -C 12 alkoxyalkyl, C 3 -C 12 cycloalkyl, C 4 -C 12 cycloalkylalkyl, aryl, C 7 -C 12 aralkyl, C 3 -C 12 heterocyclyl, C 3 -C 12 heterocyclylalkyl, C 5 -C 12 heteroaryl and C 3 -C 12 heteroarylalkyl;

R 4 and R 5 are each independently selected from hydrogen, fluoro, chloro, methyl, methoxy and trifluoromethyl; and

R 6 , R 6a , R 7 , R 7a , R 8 , R 8a , R 9 , and R 9a are each independently selected from hydrogen or C 1 -C 3 alkyl.

10. The method of claim 9 ,

wherein:

V is —C(O)—;

W is —N(R 1 )C(O)—;

R 2 is C 3 -C 12 cycloalkyl;

R 3 is aryl or C 5 -C 12 heteroaryl.

11. The method of claim 10 , wherein the skin disorder is rosacea.

12. The method of claim 10 , wherein the skin disorder is seborrheic skin.

Assignments (3)

Continuity (13)