IP Library Granted Patent US 8,772,286
Granted Patent B2
US 8,772,286 · App. 13/514,865 · Granted Jul 8, 2014

MK2 inhibitors

Inventors: Tjeerd Andries Barf (Ravenstein, NL); Arthur Oubrie (Wychen, NL); Carsten Schultz-Fademrecht (Pomezia, IT); Eduard Willem Zwart (Oss, NL); Niels Hoogenboom (Ryen, NL); Sander Martijn De Wilde (Oss, NL); Allard Kaptein (Zaltbommel, NL)
Assignee: Merck Sharp & Dohme B.V.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,772,286
App. No.
13/514,865
Granted
Jul 8, 2014
Kind
B2
Abstract

The present invention relates to compounds of general Formula (I) or a pharmaceutically acceptable salt thereof. The compounds can be used in the treatment of immune, autoimmune, inflammatory diseases, cardiovascular diseases, infectious diseases, bone resorption disorders, neurodegenerative diseases or proliferative diseases.

Claims (158)

1. A compound of Formula I,

or a pharmaceutically acceptable salt thereof, wherein

A is CH or N;

Y is a bond, or —C(O)NH—;

X is a bond, —CH 2 —, —CH 2 CH 2 —;

V is —CH 2 —, O, C(O), —CHF—, or —CF 2 —, with the proviso that if V is O, X is —CH 2 CH 2 — and that if V is C(O), X is —CH 2 ;

W is a bond or —CH 2 —;

R1 is hydrogen or F;

R2 is a (1-12C)heteroaryl or (6-10C)aryl both optionally substituted with one or more groups independently selected from R4;

R3 is a hydrogen; (3-6C)cycloalkyl; (1-6C)alkyl, —(CH 2 ) m OR5; —(CH 2 ) m NR5R6; or —C(O)CH 2 NR5R6;

R4 is taken from halogen; OH; SH; nitrile, nitro, NH 2 ; (3-6C)cycloalkyl, (3-6C)cycloalkoxy, (1-6C)alkoxy or (1-6C)alkyl, all optionally substituted with one or more halogen; phenoxy; —O(CH 2 ) m OR5, —O(CH 2 ) m NR7R8, —OC(O)R7 with the proviso that R7 is not hydrogen, —O(1-12C)heteroaryl), —S(1-6C)alkyl); —S(3-6C)cycloalkyl)-; NR7R8; —NR9(CH 2 ) m OR7, —NR9(CH 2 ) m NR7R8; (1-6C)alkylcarbonyl; (3-6C)cycloalkylcarbonyl; —C(O)NR7R8; —C(O)NR9(CH 2 ) m NR7R8, —C(O)NR9(CH 2 ) m OR7, —C(O)OR7, —SO 2 (1-6C)alkyl), —SO 2 (3-6C)cycloalkyl); —O(1-6C)alkyl)O— where the oxygens are attached to the (1-12C)heteroaryl or (6-10C)aryl ring on two neighboring carbons; phenyl or (1-12C)heteroaryl;

R5 is hydrogen (3-6C)cycloalkyl; or (1-6C)alkyl;

R6 is hydrogen; (3-6C)cycloalkyl; (1-6C)alkyl; or (1-6C)alkylcarbonyl;

R7 is hydrogen, (1-6C)alkyl or (3-6C)cycloalkyl;

R8 is hydrogen; (3-6C)cycloalkyl; (1-6C)alkyl; or (1-6C)alkylcarbonyl; or

R7 and R8 together with the nitrogen to which they are bonded in NR7R8 can form a 5-7-membered at least one nitrogen containing (4-6C)heterocyclyl ring which optionally contains one additional heteroatom selected from N, O or S;

R9 is hydrogen; (1-6C)alkyl or (3-6)cycloalkyl; and

m is 2 or 3.

2. The compound according to claim 1 , wherein

V is —(CH 2 )— or O, with the proviso that if V is O, X is —CH 2 CH 2 —;

R4 is taken from halogen; OH; NH 2 ; (3-6C)cycloalkyl or (1-6C)alkyl, both optionally substituted with one or more halogen; (3-6C)cycloalkoxy; (1-6C)alkoxy; phenoxy; —NR7R8; (1-6C)alkylcarbonyl; (3-6C)cycloalkylcarbonyl; —C(O)NR7R8; —O(1-6C)alkyl)O— where the oxygens are attached to the (1-12C)heteroaryl or (6-10C)aryl ring on two neighboring carbons; phenyl or (1-5C)heteroaryl.

3. The compound according to claim 1 , wherein V is —CH 2 —.

4. The compound according to claim 1 , wherein W is —CH 2 —.

5. The compound according to claim 1 , wherein X is —CH 2 —.

6. The compound according to claim 1 , wherein R2 is (1-5C)heteroaryl optionally substituted with one or more groups independently selected from R4 wherein R4 is selected from —NR7R8; NH 2 or (1-6C)alkoxy.

7. The compound according to claim 1 , wherein R2 is phenyl optionally substituted with one or more groups independently selected from R4 wherein

R4 is taken from halogen; OH; (3-6C)cycloalkyl or (1-6C)alkyl, both optionally substituted with one or more halogen; (1-6C)alkoxy; phenoxy; (1-6C)alkylcarbonyl; (3-6C)cycloalkylcarbonyl; —C(O)NR7R8; —O(1-6C)alkyl)O— where the oxygens are attached to the (hetero)aryl ring on two neighboring carbons or phenyl.

8. The compound according to claim 1 , wherein R3 is hydrogen; —(CH 2 ) m NR5R6, or —C(O)CH 2 NR5R6.

9. The compound according to claim 8 wherein R3 is hydrogen.

10. The compound according to claim 1 , wherein R3 is methyl, and Y=—C(O)NH—.

11. The compound according to claim 1 , wherein Y is a bond.

12. A pharmaceutical composition which comprises a compound of formula I according to claim 1 or a pharmaceutically acceptable salt thereof and one or more pharmaceutically acceptable excipients.

13. A method of inhibiting MK2 activity comprising contacting a cell with a compound of formula I according to claim 1 , or a pharmaceutically acceptable salt thereof.

14. A compound according to claim 1 selected from the group consisting of:

2′-(2-(benzofuran-2-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2′-amino-2,5′-bipyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(5-methoxypyridin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(2-fluorophenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(3-fluorophenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(4-acetylphenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzo[d][1,3]dioxol-5-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

N-(5-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyrimidin-2-yl)pyridin-2-yl)acetamide;

N-(5-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyrimidin-2-yl)pyridin-2-yl)propionamide;

2′-(2-(3-chloro-4-(trifluoromethyl)phenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(3,4-dihydro-2H-benzo[b][1,4]dioxepin-7-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(biphenyl-4-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(3,4-dichlorophenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(3-isopropylphenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(4-phenoxyphenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(3-(trifluoromethoxy)phenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(4-(trifluoromethyl)phenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(4-cyclohexylphenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(3-tert-butyl-5-methylphenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(4-hydroxy-3-methoxyphenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(quinolin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(4-tert-butylphenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(4-isobutylphenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(naphthalen-2-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(3,5-dichlorophenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(dibenzo[b,d]furan-2-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(4-isobutoxyphenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzo[b]thiophen-2-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

3-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyrimidin-2-yl)benzamide;

2′-(2-(3-acetylphenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2-chloro-N-cyclohexyl-4-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyrimidin-2-yl)benzamide;

2′-(2-(4-chloro-2-fluorophenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(biphenyl-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(3,5-bis(trifluoromethyl)phenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(3-(trifluoromethyl)phenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

N-cyclohexyl-4-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyrimidin-2-yl)benzamide;

2′-(2-(benzofuran-2-yl)pyrimidin-4-yl)-1-methyl-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzofuran-2-yl)pyrimidin-4-yl)-1-methyl-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzofuran-2-yl)pyrimidin-4-yl)-1-ethyl-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

1-(2-aminoethyl)-2′-(2-(benzofuran-2-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

N-(2-(2′-(2-(benzofuran-2-yl)pyrimidin-4-yl)-4′-oxo-1′,4′, 5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-1-yl)ethyl)acetamide;

N-(3-(2′-(2-(benzofuran-2-yl)pyrimidin-4-yl)-4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-1-yl)propyl)acetamide;

2′-(2-(benzofuran-2-yl)-5-fluoropyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzo[d][1,3]dioxol-5-yl)-5-fluoropyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(5-fluoro-2-(quinolin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

4-(5-fluoro-4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyrimidin-2-yl)-N-methylbenzamide;

2′-(2-(4-chloro-2-fluorophenyl)-5-fluoropyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzofuran-2-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzo[d][1,3]dioxol-5-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzo[d][1,3]dioxol-5-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[pyrrolidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-p-tolylpyrimidin-4-yl)-5′,6′-dihydrospiro[pyrrolidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(3-fluorophenyl)pyrimidin-4-yl)-5′,6′-dihydrospiro[pyrrolidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzofuran-2-yl)pyridin-4-yl)-5′,6′-dihydrospiro[pyrrolidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzofuran-2-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[morpholine-2,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzofuran-2-yl)pyridin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(quinolin-3-yl)pyridin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzo[d][1,3]dioxol-5-yl)pyridin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzo[d]thiazol-2-yl)pyridin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(benzo[d]thiazol-2-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(thiazol-2-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

1-(2-aminoacetyl)-2′-(2-(benzofuran-2-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2′-(cyclopentylamino)-2,5′-bipyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-4-(trifluoromethyl)benzamide;

3,4-dimethyl-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyrimidin-2-yl)-4-(trifluoromethyl)benzamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyrimidin-2-yl)-3-(trifluoromethoxy)benzamide; 2′-(2-(6-aminopyridin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(pyridin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(pyridin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

(S)-2′-(2-(pyridin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

(R)-2′-(2-(pyridin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(6-(3-methoxypropoxy)pyridin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

(S)-2′-(2-(6-(3-methoxypropoxy)pyridin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

(R)-2′-(2-(6-(3-methoxypropoxy)pyridin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2-(5-methoxypyridin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

(S)-2′-(2-(5-methoxypyridin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

(R)-2′-(2-(5-methoxypyridin-3-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

2′-(2′-(cyclopentylamino)-2,5′-bipyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one;

3,4-dimethyl-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyrimidin-2-yl)benzamide;

3,4-dimethyl-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

3-fluoro-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

3-fluoro-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)picolinamide;

4-fluoro-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyrimidin-2-yl)benzamide;

4-fluoro-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyrimidin-2-yl)-2-naphthamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-2-naphthamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyrimidin-2-yl)-1-naphthamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-1-naphthamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)biphenyl-4-carboxamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-4-(trifluoromethyl)benzamide;

3-(dimethylamino)-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)isonicotinamide;

6-methoxy-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)picolinamide;

3,4-dimethyl-N-(4-(1-methyl-4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

3,4-dimethyl-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

(S)-3,4-dimethyl-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

(R)-3,4-dimethyl-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

3,4-dimethyl-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[pyrrolidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

N-(4-(1-methyl-4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-3-(trifluoromethoxy)benzamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-3-(trifluoromethoxy)benzamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[pyrrolidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-3-(trifluoromethoxy)benzamide;

3-fluoro-N-(4-(1-methyl-4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

3-fluoro-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

3-fluoro-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[pyrrolidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)picolinamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[pyrrolidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)picolinamide;

4-fluoro-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

(S)-4-fluoro-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

(R)-4-fluoro-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

4-fluoro-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[pyrrolidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

N-(4-(1-methyl-4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-4,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-2-naphthamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-2-naphthamide;

(S)—N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-2-naphthamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[pyrrolidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-2-naphthamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-3-(trifluoromethyl)benzamide;

3,5-difluoro-N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)benzamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-1-naphthamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)quinoline-2-carboxamide;

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)isoquinoline-1-carboxamide; and

N-(4-(4′-oxo-1′,4′,5′,6′-tetrahydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridine]-2′-yl)pyridin-2-yl)-4-(trifluoromethyl)benzamide, and

(S)-2′-(2-(benzo[d][1,3]dioxol-5-yl)pyrimidin-4-yl)-5′,6′-dihydrospiro[piperidine-3,7′-pyrrolo[3,2-c]pyridin]-4′(1′H)-one,

or a pharmaceutically acceptable salt thereof.

15. A method of treating a disease selected from the group consisting of prostate cancer, skin cancer, bladder cancer, multiple myeloma, and metatstatic melanoma, in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of formula I according to claim 1 or a pharmaceutically acceptable salt thereof, so as to thereby treat the subject.

16. A method of treating a disease selected from the group consisting of rheumatoid arthritis, psoriasis and inflammatory bowel disease, in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of formula I according to claim 1 or a pharmaceutically acceptable salt thereof, so as to thereby treat the subject.

Assignments (6)
MERGER Recorded Jan 29, 2014
From: N.V. ORGANON
To: MSD OSS B.V.
Reel/Frame 032134/0225 →
MERGER Recorded Jan 29, 2014
From: MSD OSS B.V.
To: ORGANON BIOSCIENCES NEDERLAND B.V.
Reel/Frame 032134/0300 →
MERGER Recorded Jan 29, 2014
From: ORGANON BIOSCIENCES NEDERLAND B.V.
To: MERCK SHARP & DOHME B.V.
Reel/Frame 032134/0426 →
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY DATA NAME FROM MERCK SHARP & DOHME B.V. PREVIOUSLY RECORDED ON REEL 031059 FRAME 0001. ASSIGNOR(S) HEREBY CONFIRMS THE CORRECT NAME SHOULD BE MERCK SHARP & DOHME OSS B.V.. Recorded Sep 5, 2013
From: N.V. ORGANON
To: MERCK SHARP & DOHME OSS B.V.
Reel/Frame 031170/0382 →
CHANGE OF NAME Recorded Aug 21, 2013
From: N.V. ORGANON
To: MERCK SHARP & DOHME B.V.
Reel/Frame 031059/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2013
From: BARF, TJEERD ANDRIES; OUBRIE, ARTHUR; SCHULTZ-FADEMRECHT, CARSTEN; ZWART, EDUARD WILLEM; HOOGENBOOM, NIELS; DEWILDE, SANDER MARTIJN; KAPTEIN, ALLARD
To: N.V. ORGANON
Reel/Frame 031006/0063 →
Priority Claims (1)
EP 09179043 · Dec 14, 2009 · regional
Continuity (2)
Provisional Application 61286091 · Dec 14, 2009
Related Publication 20120245175A1 · Sep 27, 2012