IP Library Granted Patent US 8,034,945
Granted Patent B2
US 8,034,945 · App. 11/912,746 · Granted Oct 11, 2011

4-phenyl-5-OXO-1,4,5,6,7,8-hexahydroquinoline derivatives as medicaments for the treatment of infertility

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Quick Facts
Patent No.
US 8,034,945
App. No.
11/912,746
Granted
Oct 11, 2011
Kind
B2
Abstract

The invention relates to a 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative according to Formula (I), wherein the substituents are defined as in the description, or a pharmaceutically salt thereof. The compounds of this invention are potent FSH receptor activators and may be used for treating fertility disorders in e.g. controlled ovarian hyperstimulation and IVF procedures.

Claims (29)

1. A 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative according to Formula I,

wherein

R 1 is (1-6C)alkyl, (2-6C)alkenyl or (2-6C)alkynyl;

R 2 is halogen, (1-4C)alkoxy, fluorinated (1-4C)alkoxy, (1-4C)alkyl, or fluorinated (1-4C)alkyl; or R 2 may be H when R 3 is R 9 ,R 10 -aminosulfonyl;

R 3 is OH, NO 2 , CN, fluorinated (1-4C)alkoxy, (1-4C)alkoxy(2-4C)alkoxy, hydroxy(2-4C)alkoxy, (1-4C)alkoxycarbonyl, (3-4C)alkenyloxycarbonyl, (1-4C)alkoxycarbonyloxy, (3-4C)alkenyloxycarbonyloxy, R 7 ,R 8 -amino, R 9 ,R 10 -amino, R 9 ,R 10 -aminocarbonyl, R 9 ,R 10 -aminosulfonyl or phenyl(1-4C)alkoxy, wherein the phenyl ring is optionally substituted with one or more substituents selected from hydroxy, amino, halogen, nitro, trifluoromethyl, cyano, (1-4C)alkyl, (2-4C)alkenyl, (2-4C)alkynyl, (1-4C)alkoxy, (di)(1-4C)alkylamino;

R 4 is R 11 -phenyl or R 11 -(2-5C)heteroaryl, wherein the phenyl or heteroaryl group is optionally further substituted with one or more substituents selected from hydroxy, amino, halogen, nitro, trifluromethyl, cyano, (1-4C)alkyl, (1-4C)alkylthio, (1-4C)alkoxy, (2-4C)alkenyl, (2-4C)alkynyl;

R 7 is H, (1-4C)alkyl;

R 8 is (1-4C)alkylsulfonyl, (1-4C)alkylcarbonyl, (2-4C)alkenylcarbonyl, (3-6C)cycloalkylcarbonyl, (1-4C)alkoxycarbonyl, (3-4C)alkenyloxycarbonyl, (1-4C)alkoxy(1-4C)alkylcarbonyl, (3-4C)alkenyloxy(1-4C)alkylcarbonyl phenylcarbonyl, (2-5C)heteroarylcarbonyl, phenyl(1-4C)alkylcarbonyl, (2-5C)heteroaryl(1-4C)alkylcarbonyl, wherein the phenyl ring or the heteroaromatic ring is optionally substituted with one or more substituents selected from hydroxy, amino, halogen, nitro, trifluoromethyl, cyano, (1-4C)alkyl, (2-4C)alkenyl, (2-4C)alkynyl, (1-4C)alkoxy, (di)(1-4C)alkylamino;

R 9 and R 10 are independently selected from H, (1-6C)alkyl, (3-6C)cycloalkyl, (3-6C)cycloalkyl(1-4C)alkyl and (1-4C)alkoxy(2-4C)alkyl;

or R 9 and R 10 may be joined in a (4-6C)heterocycloalkenyl ring or a (2-6C)heterocycloalkyl ring, optionally substituted with one or more (1-4C)alkyl substituents;

R 11 is H, (1-6C)alkoxycarbonyl, R 12 ,R 13 -amino, (1-6C)alkylcarbonyl, (1-6C)alkylsulfonyl, R 14 -oxy, R 14 ,R 15 -amino, R 14 ,R 15 -aminocarbonyl, R 14 ,R 15 -aminosulfonyl;

R 12 is H, (1-4C)alkyl;

R 13 is (1-4C)alkylsulfonyl, (1-4C)alkylcarbonyl, (3-6C)cycloalkylcarbonyl, (1-4C)alkoxycarbonyl, (3-4C)alkenyloxycarbonyl, (di)(1-4C)alkylamino-(1-4C)alkylcarbonyl, (2-6C)heterocycloalkyl(1-4C)alkylcarbonyl, (4-6C)heterocyclo-alkenyl(1-4C)alkylcarbonyl or (1-4C)alkoxy(1-4C)alkylcarbonyl;

R 14 and R 15 are independently selected from H, (1-6C)alkyl, (3-4C)alkenyl, (3-4C)alkynyl, (3-6C)cycloalkyl, (3-6C)cycloalkyl(1-4C)alkyl, hydroxy(2-4C)alkyl, amino(2-4C)alkyl, (1-4C)alkoxy(2-4C)alkyl, (di)(1-4C)alkylamino(2-4C)alkyl, (2-6C)heterocycloalkyl(2-4C)alkyl, (4-6C)heterocycloalkenyl(2-4C)alkyl, phenyl(1-4C)alkyl and (2-5C)heteroaryl(1-4C)alkyl;

X is O or R 16 —N;

Y is CH 2 , C(O) or SO 2 ;

Z is CN or NO 2 ;

R 16 is H, (1-4C)alkyl, (1-4C)alkylcarbonyl;

or a pharmaceutically acceptable salt thereof.

2. The 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative according to claim 1 , wherein R 1 is (1-6C)alkyl.

3. The 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative according to claim 1 , wherein R 2 is halogen.

4. The 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative according to claim 1 , wherein R 3 is R 9 ,R 10 -aminosulfonyl.

5. The 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative according to claim 4 , wherein R 9 and R 10 are independently (1-6C)alkyl.

6. The 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative according to claim 1 , wherein R 4 is R 11 -phenyl or R 11 -(2-5C)heteroaryl, wherein the phenyl or heteroaryl group is optionally further substituted with one (1-4C)alkoxy.

7. The 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative according to claim 6 , wherein R 11 is H or R 12 ,R 13 -amino.

8. The 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative according to claim 1 , wherein Z is CN.

9. The 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative according to claim 1 , wherein X is O.

10. The 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative according to claim 1 , wherein Y is CH 2 .

11. A pharmaceutical composition comprising a 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative or a pharmaceutically acceptable salt thereof according to claim 1 , and pharmaceutically suitable auxiliaries.

Assignments (4)
MERGER Recorded Mar 8, 2013
From: ORGANON BIOSCIENCES NEDERLAND B.V.
To: MERCK SHARP & DOHME B.V.
Reel/Frame 029940/0296 →
MERGER Recorded Mar 7, 2013
From: MSD OSS B.V.
To: ORGANON BIOSCIENCES NEDERLAND B.V.
Reel/Frame 029939/0001 →
MERGER Recorded Dec 1, 2011
From: N.V. ORGANON
To: MSD OSS B.V.
Reel/Frame 027307/0482 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2007
From: TIMMERS, CORNELIS MARIUS; KARSTENS, WILLEM FREDERIK JOHAN; GRIMA POVEDA, PEDRO MANUEL
To: N.V. ORGANON
Reel/Frame 020154/0234 →