IP Library Granted Patent US 8,063,102
Granted Patent B2
US 8,063,102 · App. 12/721,842 · Granted Nov 22, 2011

Tetrahydronaphthalen-2-ol derivatives

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Quick Facts
Patent No.
US 8,063,102
App. No.
12/721,842
Granted
Nov 22, 2011
Kind
B2
Abstract

The present invention relates to novel tetrahydronaphthalen-2-ol derivatives, to pharmaceutical compositions comprising these compounds and to their use in therapy, in particular to their use for the manufacture of a medicament for the prevention or treatment of lower urinary tract symptoms, benign prostate hyperplasia, prostate cancer, hot flushes, anxiety, depression, breast cancer, medullary thyroid carcinoma, ovarian cancer, inflammatory bowel disease, arthritis, endometriosis, and colon cancer.

Claims (34)

1. A tetrahydronaphthalen-2-ol derivative according to Formula 1

wherein

R1 is (C1-C4)alkyl, (C2-C4)alkenyl or (C2-C4)alkynyl, independently optionally substituted with one or more halogen, R1 having a cis-orientation in relation to both the exocyclic phenyl group at the 6-position and the benzyl group at the 8-position of the skeleton;

R2-R13 are independently H, halogen, CN, OH, (C1-C4)alkyl, optionally substituted with one or more halogen, or (C1-C2)alkyloxy;

or a prodrug or an isotopically-labelled derivative thereof.

2. A tetrahydronaphthalen-2-ol derivative according to claim 1 , wherein R1 is (C1-C4)alkyl, optionally substituted with one or more halogen.

3. A tetrahydronaphthalen-2-ol derivative of Formula 1 according to claim 1

wherein

R1 is (C1-C4)alkyl, (C2-C4)alkenyl or (C2-C4)alkynyl, independently optionally substituted with one or more halogen, R1 having a cis-orientation in relation to both the exocyclic phenyl group at the 6-position and the benzyl group at the 8-position of the skeleton;

R2-R6 are independently H, halogen, CN, OH, (C1-C4)alkyl, optionally substituted with one or more halogen or (C1-C2)alkoxy, with a maximum of two OH groups;

R7-R13 are independently H, halogen, CN, (C1-C4)alkyl, optionally substituted with one or more halogen or (C1 -C2)alkoxy;

or a prodrug thereof.

4. A tetrahydronaphthalen-2-ol derivative of Formula 1 according to claim 1

wherein

R1 is (C1-C4)alkyl, (C2-C4)alkenyl or (C2-C4)alkynyl, independently optionally substituted with one or more halogen, R1 having a cis-orientation in relation to both the exocyclic phenyl group at the 6-position and the benzyl group at the 8-position of the skeleton;

R2-R13 are independently H, halogen, CN, OH, (C1-C4)alkyl, optionally substituted with one or more halogen or (C1-C2)alkoxy, with a maximum of five R2-R13 groups unequal to H.

5. A tetrahydronaphthalen-2-ol derivative of Formula 1 according to claim 1

wherein

R1 is methyl, ethyl or propyl;

R2 is H, chlorine, fluorine, CN, methoxy or methyl;

R3-R7 and R10 are H or fluorine;

R8, R9, R11 and R13 are H;

R12 is H, fluorine or methyl.

6. A tetrahydronaphthalen-2-ol derivative of Formula 2 according to claim 1

wherein

R1 is methyl, ethyl or propyl;

R2 is H, chlorine, fluorine, CN, methoxy or methyl;

R3-R7 and R10 are H or fluorine;

R8, R9, R11 and R13 are H;

R12 is H, fluorine or methyl.

7. A tetrahydronaphthalen-2-ol derivative according to claim 6 selected from the group consisting of compounds according to Formula 2 wherein R1 is methyl, R2 is fluorine, and R3-R13 are H; R1 is ethyl, R2 is fluorine, and R3-R13 are H; R1 is methyl, R2 and R6 are fluorine, and R3-R5 and R7-R13 are H; R1 is methyl, R2 is CN, and R3-R13 are H; R1 is ethyl, R2 and R12 are fluorine, and R3-R11 and R13 are H; and R1 is ethyl, R4 is fluorine, and R2-R3 and R5-R13 are H.

8. A tetrahydronaphthalen-2-ol derivative according to claim 7 , wherein R1 is methyl, R2 is fluorine, and R3-R13 are H.

9. A pharmaceutical composition comprising a tetrahydronaphthalen-2-ol derivative according to claim 1 and one or more pharmaceutically acceptable excipients.

10. A method for the treatment of a mammal suffering from a disease or disorder selected from the group consisting of lower urinary tract symptoms, benign prostate hyperplasia, and prostate cancer, the method comprising administering a therapeutically effective amount of a tetrahydronaphthalen-2-ol derivative according to claim 1 .

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 Oct 1, 2010
From: STOCK, HERMAN THIJS; TEERHUIS, NEELTJE MIRANDA; VEENEMAN, GERRIT HERMAN
To: N.V. ORGANON
Reel/Frame 025078/0971 →