IP Library Granted Patent US 7,723,323
Granted Patent B2
US 7,723,323 · App. 12/038,255 · Granted May 25, 2010

Pharmaceutical use of fused 1,2,4-triazoles

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Quick Facts
Patent No.
US 7,723,323
App. No.
12/038,255
Granted
May 25, 2010
Kind
B2
Abstract

The use of fused 1,2,4-triazoles for modulating the activity of 11β-hydroxysteroid dehydrogenase type 1 (11βHSD1) and the use of these compounds as pharmaceutical compositions has been described. Also a novel class of fused 1,2,4-triazoles, their use in therapy, pharmaceutical compositions comprising the compounds, as well as their use in the manufacture of medicaments has been described. The present compounds are modulators and more specifically inhibitors of the activity of 11βHSD1 and may be useful in the treatment, prevention and/or prophylaxis of a range of medical disorders where a decreased intracellular concentration of active glucocorticoid is desirable.

Claims (35)

1. A compound of formula (II)

wherein

R 1 is aryl or hetaryl, wherein the aryl and hetaryl groups independently are optionally substituted with one or more of R 7 ;

R 2 and R 3 are connected to one of the following ring systems at the carbon atoms marked with an asterix (*)

wherein the ring systems independently are optionally substituted with one or more R 8 ;

R 7 is hydrogen, halo, hydroxy, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 alkyloxy, trihalomethyl, trihalomethoxy, aryloxy, hetaryloxy, NR 9 R 10 , arylC 1 -C 6 alkyloxy, hetarylC 1 -C 6 alkyloxy, C 1 -C 6 alkyloxyC 1 -C 6 alkyl, aryloxyC 1 -C 6 alkyl, arylC 1 -C 6 alkyloxyC 1 -C 6 alkyl, C 1 -C 6 alkylcarbonyl, arylcarbonyl, hetarylcarbonyl, arylC 1 -C 6 alkylcarbonyl, hetarylC 1 -C 6 alkylcarbonyl, C 1 -C 6 alkyl-carboxy, arylcarboxy, hetarylcarboxy, arylC 1 -C 6 alkylcarboxy or hetarylC 1 -C 6 alkylcarboxy;

R 8 is hydrogen, C 1 -C 6 alkyl, halo, aryl, hetaryl, arylC 1 -C 6 alkyl, NR 9 R 10 , trihalomethyl, trihalomethoxy, hydroxy, oxo, C 1 -C 6 alkyloxy, aryloxy, arylC 1 -C 6 alkyloxy, hetarylC 1 -C 6 alkyloxy, C 1 -C 6 alkyloxyC 1 -C 6 alkyl, C 1 -C 6 alkylcarbonyl, arylcarbonyl, arylC 1 -C 6 alkylcarbonyl, C 1 -C 6 alkylcarboxy, arylcarboxy or arylC 1 - C 6 alkylcarboxy;

R 9 and R 10 independently are hydrogen, C 1 -C 6 alkyl, aryl or arylC 1 -C 6 alkyl wherein the alkyl and aryl groups independently are optionally substituted with one or more of R 11 ; or

R 9 and R 10 together with the nitrogen to which they are attached, are forming a saturated or partially saturated cyclic, bicyclic or tricyclic ring system containing from 4 to 10 carbon atoms and from 0 to 2 additional heteroatoms selected from nitrogen, oxygen or sulfur, the ring system optionally being substituted with at least one of C 1 -C 6 alkyl, aryl, hetaryl, arylC 1 -C 6 alkyl, hydroxy, oxo, C 1 -C 6 alkyloxy, arylC 1 -C 6 alkyloxy, C 1 -C 6 alkyloxyC 1 -C 6 alkyl, C 1 -C 6 alkylcarbonyl, arylcarbonyl, arylC 1 -C 6 alkylcarbonyl, C 1 -C 6 alkylcarboxy, arylcarboxy or arylC 1 -C 6 alkylcarboxy;

R 11 is C 1 -C 6 alkyl, oxo or halo;

X is (CR 12 R 13 ) n , wherein R 12 and R 13 independently are hydrogen, oxo, hydroxy or C 1 -C 6 alkyl; and

n is 1 or 2; or

a salt thereof with a pharmaceutically acceptable acid or base, or optical isomer or mixture of optical isomers, racemic mixture, or tautomeric form thereof.

2. A compound according to claim 1 , wherein R 1 is aryl optionally substituted with R 7 .

3. A compound according to claim 2 , wherein R 1 is phenyl optionally substituted with R 7 .

4. A compound according to claim 1 , wherein R 7 is hydrogen, halo, hydroxy, cyano, C 1 -C 6 alkyl, C 1 -C 6 alkyloxy, trihalomethyl, aryloxy, arylC 1 -C 6 alkyloxy, hetarylC 1 -C 6 alkyloxy, C 1 -C 6 alkyloxyC 1 -C 6 alkyl, aryloxyC 1 -C 6 alkyl or arylC 1 -C 6 alkyloxyC 1 -C 6 alkyl.

5. A compound according to claim 1 , wherein R 8 is hydrogen, C 1 -C 6 alkyl or halo.

6. A compound of formula (III)

wherein

R 1 is aryl or hetaryl, wherein the aryl and hetaryl groups independently are optionally substituted with one or more of R 7 ;

R 7 is hydrogen, halo, hydroxy, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 alkyloxy, trihalomethyl, trihalomethoxy, aryloxy, hetaryloxy, NR 9 R 10 , arylC 1 -C 6 alkyloxy, hetarylC 1 -C 6 alkyloxy, C 1 -C 6 alkyloxyC 1 -C 6 alkyl, aryloxyC 1 -C 6 alkyl, arylC 1 -C 6 alkyloxyC 1 -C 6 alkyl, C 1 -C 6 alkylcarbonyl, arylcarbonyl, hetarylcarbonyl, arylC 1 -C 6 alkylcarbonyl, hetarylC 1 -C 6 alkylcarbonyl, C 1 -C 6 alkyl-carboxy, arylcarboxy, hetarylcarboxy, arylC 1 -C 6 alkylcarboxy or hetarylC 1 -C 6 alkylcarboxy;

R 9 and R 10 independently are hydrogen, C 1 -C 6 alkyl, aryl or arylC 1 -C 6 alkyl wherein the alkyl and aryl groups independently are optionally substituted with one or more of R 11 ; or

R 9 and R 10 together with the nitrogen to which they are attached, are forming a saturated or partially saturated cyclic, bicyclic or tricyclic ring system containing from 4 to 10 carbon atoms and from 0 to 2 additional heteroatoms selected from nitrogen, oxygen or sulfur, the ring system optionally being substituted with at least one of C 1 -C 6 alkyl, aryl, hetaryl, arylC 1 -C 6 alkyl, hydroxy, oxo, C 1 - C 6 alkyloxy, arylC 1 -C 6 alkyloxy, C 1 -C 6 alkyloxyC 1 -C 6 alkyl, C 1 -C 6 alkylcarbonyl, arylcarbonyl, arylC 1 -C 6 alkylcarbonyl, C 1 -C 6 alkylcarboxy, arylcarboxy or arylC 1 -C 6 alkylcarboxy;

R 11 is C 1 -C 6 alkyl, oxo or halo;

a salt thereof with a pharmaceutically acceptable acid or base, or optical isomer or mixture of optical isomers, racemic mixture, or tautomeric form thereof.

7. A compound according to claim 6 , wherein R 1 is aryl optionally substituted with R 7 .

8. A compound according to claim 6 , wherein R 1 is phenyl optionally substituted with R 7 .

9. A compound according to claim 7 , wherein R 7 is halo, hydroxy, cyano, C 1 -C 6 alkyl, C 1 -C 6 alkyloxy, trihalomethyl, trihalomethoxy, aryloxy, hetaryloxy, NR 9 R 10 , aryl C 1 -C 6 alkyloxy, hetaryl C 1 -C 6 alkyloxy, C 1 -C 6 alkyloxy C 1 -C 6 alkyl, aryloxyC 1 -C 6 alkyl, arylC 1 -C 6 alkyloxyC 1 -C 6 alkyl, C 1 -C 6 alkylcarbonyl, arylcarbonyl, hetarylcarbonyl, arylC 1 -C 6 alkylcarbonyl or hetarylC 1 -C 6 alkylcarbonyl.

10. A compound according to claim 9 , wherein R 7 is C 1 -C 6 alkyloxy, trihalomethoxy, aryloxy, hetaryloxy, arylC 1 -C 6 alkyloxy, hetarylC 1 -C 6 alkyloxy, C 1 -C 6 alkyloxyC 1 -C 6 alkyl, aryloxyC 1 -C 6 alkyl or arylC 1 -C 6 alkyloxyC 1 -C 6 alkyl.

11. A compound according to claim 1 or 6 , which is

3-(2-Phenoxymethyl-phenyl)-6,7,8,9,10,11-hexahydro-5H-5,9:7,11-dimethano [1,2,4]triazolo[4.3-a]azonine; or a

salt thereof with a pharmaceutically acceptable acid or base, or optical isomer or mixture of optical isomers, racemic mixture, or tautomeric form thereof.

12. A pharmaceutical composition comprising, as an active ingredient, at least one compound according to claim 1 or 6 , together with one or more pharmaceutically acceptable carrier or excipient.

13. The pharmaceutical composition according to claim 12 , which is for oral, nasal, buccal, transdermal, pulmonal or parenteral administration.

14. The pharmaceutical composition according to claim 12 , in unit dosage form, comprising from 0.05 mg to 2000 mg of the compound.

Assignments (7)
NOTICE OF RELEASE OF SECURITY INTEREST IN PATENTS FOR REEL/FRAME 030982/0793 Recorded Apr 7, 2014
From: M&F TTP HOLDINGS LLC
To: HIGH POINT PHARMACEUTICALS, LLC
Reel/Frame 032621/0867 →
SECURITY AGREEMENT Recorded Aug 9, 2013
From: HIGH POINT PHARMACEUTICALS, LLC
To: M&F TTP HOLDINGS LLC C/O MACANDREWS & FORBES HOLDINGS INC.
Reel/Frame 030982/0793 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2010
From: TRANSTECH PHARMA, INC.
To: HIGH POINT PHARMACEUTICALS, LLC
Reel/Frame 024331/0364 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2010
From: NOVO NORDISK A/S
To: TRANSTECH PHARMA, INC.
Reel/Frame 024331/0312 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2010
From: ANDERSEN, HENRIK SUNE; KAMPEN, GITA CAMILLA TEJLGAARD; CHRISTENSEN, INGE THOGER; MOGENSEN, JOHN PATRICK; LARSEN, ANNETTE ROSENDAL
To: NOVO NORDISK A/S
Reel/Frame 024331/0280 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 27, 2009
From: TRANSTECH PHARMA, INC.
To: HIGH POINT PHARMACEUTICALS, LLC
Reel/Frame 022596/0244 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2009
From: NOVO NORDISK A/S
To: TRANSTECH PHARMA, INC.
Reel/Frame 022566/0174 →