IP Library Granted Patent US 10,100,056
Granted Patent B2
US 10,100,056 · App. 14/772,737 · Granted Oct 16, 2018

SHIP1 modulators and methods related thereto

Inventors: Lloyd F. Mackenzie (North Vancouver, CA); Curtis Harwig (Vancouver, CA); David Bogucki (Surrey, CA); Jeffery R. Raymond (Vancouver, CA); Jeremy D. Pettigrew (Burnaby, CA)
Assignee: Aquinox Pharmaceuticals (Canada) Inc.
C07D473/34C07C215/42C07C225/10C07C233/23C07C233/74C07C255/31C07C275/24C07C279/08C07C311/04C07D207/06C07D207/335C07D209/08C07D213/38C07D213/64C07D231/12C07D233/60C07D239/34C07D241/18C07D249/08C07D295/096C07D317/46
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 10,100,056
App. No.
14/772,737
Granted
Oct 16, 2018
Kind
B2
Abstract

Compounds of formula (I): where R 1 , R 2 , R 3 , R 4a , R 4b , R 5 , R 6 and R 7 are defined herein, or stereoisomers or pharmaceutically acceptable salts thereof, are described herein. Such compounds have activity as SHIP1 modulators, and thus may be used to treat any of a variety of diseases, disorders or conditions that would benefit from SHIP1 modulation. Compositions comprising a compound of formula (I) in combination with a pharmaceutically acceptable carrier or diluent are also disclosed, as are methods of SHIP1 modulation by administration of such compounds to an animal in need thereof.

Claims (62)

1. A compound of formula (I):

wherein:

C1, C4, C11 and C12 are each independently substituted with two hydrogens;

C9 is substituted with one hydrogen;

C14 is substituted with one hydrogen when R 5 is not a direct bond to C14;

C15 is substituted with two hydrogens when R 7 is not a direct bond to C15, and one hydrogen when R 7 is a direct bond to C15;

R 1 is —R 8 —OR 9 or —R 8 —N(R 9 ) 2 ;

R 2 is —R 8 —OR 9 , —R 8 —CN, —R 8 —C(O)OR 9 , —R 8 —C(O)N(R 9 ) 2 , —R 8 —N(R 9 ) 2 , —R 8 —N(R 9 )C(O)R 9 , optionally substituted heterocyclylalkyl or optionally substituted heteroarylalkyl;

R 4a and R 4b together form methylene;

R 3 is —CH 2 —N(H)CH 2 -(2,2-difluorobenzodioxolyl), —CH 2 —CH 2 —N(4-methoxybenzyl) 2 , —CH 2 —CH 2 —N(H)-(4-methoxy)benzyl, —CH 2 —N(H)-(2-fluoro-4-methoxy)benzyl, —CH 2 —N(H)-(2-fluoro-4-methyl)benzyl, —CH 2 —N(H)-(2-methoxy-4-fluoro)benzyl, —CH 2 —N(H)-(2-methyl-4-fluoro)benzyl, —CH 2 —N(H)-(3,5-dimethoxy)benzyl, —CH 2 —N(H)-(4-fluoro)benzyl, —CH 2 —N(H)-(4-methoxy)benzyl, —CH 2 —N(H)-(4-trifluoromethyl)benzyl, —CH 2 —N(H)-(4-benzoyl)benzyl, —CH 2 —N(H)CH 2 -benzimidazolyl, —CH 2 —CH 2 —N(H)CH 2 -benzodioxolyl or —CH 2 —N(H)CH 2 CH 2 -(4-methoxy)phenyl;

R 5 is alkyl or R 5 is a direct bond to C14;

R 6 is hydrogen;

R 7 is hydrogen, —R 8 —OR 9 or a direct bond to C15;

each R 8 is independently a direct bond or a straight or branched alkylene chain; and

each R 9 is independently hydrogen, alkyl, haloalkyl, optionally substituted cycloalkyl, optionally substituted cycloalkylalkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heterocyclyl, optionally substituted heterocyclylalkyl, optionally substituted heteroaryl or optionally substituted heteroarylalkyl;

or a stereoisomer, enantiomer or tautomer thereof or mixtures thereof;

or a pharmaceutically acceptable salt or solvate thereof.

2. The compound of claim 1 wherein:

C1, C4, C11 and C12 are each independently substituted with two hydrogens;

C9 is substituted with one hydrogen;

C14 is substituted with one hydrogen;

C15 is substituted with two hydrogens;

R 1 is —R 8 —OR 9 ;

R 2 is —R 8 —OR 9 ;

R 4a and R 4b together form methylene;

R 3 is —CH 2 —N(H)CH 2 -(2,2-difluorobenzodioxolyl), —CH 2 —CH 2 —N(4-methoxybenzyl) 2 , —CH 2 —CH 2 —N(H)-(4-methoxy)benzyl, —CH 2 —N(H)-(2-fluoro-4-methoxy)benzyl, —CH 2 —N(H)-(2-fluoro-4-methyl)benzyl, —CH 2 —N(H)-(2-methoxy-4-fluoro)benzyl, —CH 2 —N(H)-(2-methyl-4-fluoro)benzyl, —CH 2 —N(H)-(3,5-dimethoxy)benzyl, —CH 2 —N(H)-(4-fluoro)benzyl, —CH 2 —N(H)-(4-methoxy)benzyl, —CH 2 —N(H)-(4-trifluoromethyl)benzyl, —CH 2 —N(H)-(4-benzoyl)benzyl, —CH 2 —N(H)CH 2 -benzimidazolyl, —CH 2 —CH 2 —N(H)CH 2 -benzodioxolyl or —CH 2 —N(H)CH 2 CH 2 -(4-methoxy)phenyl;

R 5 is alkyl;

R 6 is hydrogen;

R 7 is hydrogen;

each R 8 is independently a direct bond or a straight or branched alkylene chain; and

each R 9 is independently hydrogen, alkyl, haloalkyl, optionally substituted cycloalkyl, optionally substituted cycloalkylalkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heterocyclyl, optionally substituted heterocyclylalkyl, optionally substituted heteroaryl or optionally substituted heteroarylalkyl.

3. The compound of claim 2 wherein:

C1, C4, C11 and C12 are each independently substituted with two hydrogens;

C9 is substituted with one hydrogen;

C14 is substituted with one hydrogen;

C15 is substituted with two hydrogens;

R 1 is —OH;

R 2 is —OH or —CH 2 OH;

R 4a and R 4b together form methylene;

R 3 is —CH 2 —N(H)CH 2 -(2,2-difluorobenzodioxolyl), —CH 2 —CH 2 —N(4-methoxybenzyl) 2 , —CH 2 —CH 2 —N(H)-(4-methoxy)benzyl, —CH 2 —N(H)-(2-fluoro-4-methoxy)benzyl, —CH 2 —N(H)-(2-fluoro-4-methyl)benzyl, —CH 2 —N(H)-(2-methoxy-4-fluoro)benzyl, —CH 2 —N(H)-(2-methyl-4-fluoro)benzyl, —CH 2 —N(H)-(3,5-dimethoxy)benzyl, —CH 2 —N(H)-(4-fluoro)benzyl, —CH 2 —N(H)-(4-methoxy)benzyl, —CH 2 —N(H)-(4-trifluoromethyl)benzyl, —CH 2 —N(H)-(4-benzoyl)benzyl, —CH 2 —N(H)CH 2 -benzimidazolyl, —CH 2 —CH 2 —N(H)CH 2 -benzodioxolyl or —CH 2 —N(H)CH 2 CH 2 -(4-methoxy)phenyl;

R 5 is methyl;

R 6 is hydrogen; and

R 7 is hydrogen.

4. The compound of claim 3 selected from:

(4-((((3aS,4R,5S,7aS)-5-((1R,2S,4S)-4-hydroxy-2-(hydroxymethyl)-1-methylcyclohexyl)-7a-methyl-1-methyleneoctahydro-1H-inden-4-yl)methylamino)methyl)phenyl)(phenyl)methanone;

(1S,3S,4R)-4-((3aS,4R,5S,7aS)-4-((4-fluorobenzylamino)methyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-3-(hydroxymethyl)-4-methylcyclohexanol;

(1S,3S,4R)-3-(hydroxymethyl)-4-((3aS,4R,5S,7aS)-4-((4-methoxybenzylamino)methyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-4-methylcyclohexanol;

(1S,3S,4R)-3-(hydroxymethyl)-4-methyl-4-((3aS,4R,5S,7aS)-7a-methyl-1-methylene-4-((4-(trifluoromethyl)benzylamino)methyl)octahydro-1H-inden-5-yl)cyclohexanol;

(1S,3S,4R)-4-((3aS,4R,5S,7aS)-4-((3,5-dimethoxybenzylamino)methyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-3-(hydroxymethyl)-4-methylcyclohexanol;

(1S,3S,4R)-4-((3aS,4R,5S,7aS)-4-(((1H-benzo[d]imidazol-2-yl)methylamino)methyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-3-(hydroxymethyl)-4-methylcyclohexanol;

(1S,3S,4R)-4-((3aS,4R,5S,7aS)-4-(((2,2-difluorobenzo[d][1,3]dioxol-5-yl)methylamino)methyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-3-(hydroxymethyl)-4-methylcyclohexanol;

(1S,3S,4R)-4-((3aS,4R,5S,7aS)-4-((4-fluoro-2-methylbenzylamino)methyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-3-(hydroxymethyl)-4-methylcyclohexanol;

(1S,3S,4R)-4-((3aS,4R,5S,7aS)-4-((2-fluoro-4-methoxybenzylamino)methyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-3-(hydroxymethyl)-4-methylcyclohexanol;

(1S,3S,4R)-4-((3aS,4R,5S,7aS)-4-((4-fluoro-2-methoxybenzylamino)methyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-3-(hydroxymethyl)-4-methylcyclohexanol;

(1S,3S,4R)-4-((3aS,4R,5S,7aS)-4-((2-fluoro-4-methylbenzylamino)methyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-3-(hydroxymethyl)-4-methylcyclohexanol;

(1S,3S,4R)-4-((3aS,4S,5S,7aS)-4-(2-(bis(4-methoxybenzyl)amino)ethyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-4-methylcyclohexane-1,3-diol;

(1S,3S,4R)-4-((3aS,4S,5S,7aS)-4-(2-(4-methoxybenzylamino)ethyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-4-methylcyclohexane-1,3-diol;

(1S,3S,4R)-3-(hydroxymethyl)-4-((3aS,4R,5S,7aS)-4-((4-methoxyphenethylamino)methyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-4-methylcyclohexanol; and

(1S,3S,4R)-4-((3aS,4S,5S,7aS)-4-(2-(benzo[d][1,3]dioxol-5-ylmethylamino)ethyl)-7a-methyl-1-methyleneoctahydro-1H-inden-5-yl)-4-methylcyclohexane-1,3-diol.

5. A composition comprising a compound of formula (I) as described in claim 1 , or a stereoisomer, enantiomer or tautomer thereof or mixtures thereof; or a pharmaceutically acceptable salt or solvate thereof, and a pharmaceutically acceptable excipient.

6. A method for modulating SHIP1 comprising administering an effective amount of a compound of formula (I) as described in claim 1 , or a stereoisomer, enantiomer or tautomer thereof or mixtures thereof; or a pharmaceutically acceptable salt or solvate thereof, to a mammal in need thereof.

7. A method for treating a disease, disorder or condition that would benefit from SHIP1 modulation comprising administering an effective amount of a compound of formula (I) as described in claim 1 , or a stereoisomer, enantiomer or tautomer thereof or mixtures thereof; or a pharmaceutically acceptable salt or solvate thereof, to a mammal having said disease, disorder or condition, where the disease, disorder or condition is an autoimmune disease, disorder or condition, an inflammatory disease, disorder or condition, or a neoplastic or cell proliferative disease, disorder or condition.

Assignments (3)
MERGER Recorded Dec 13, 2021
From: TARO PHARMACEUTICALS INC.; AQUINOX PHARMACEUTICALS (CANADA) INC.
To: TARO PHARMACEUTICALS INC.
Reel/Frame 058371/0661 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 16, 2015
From: MACKENZIE, LLOYD F.; HARWIG, CURTIS; BOGUCKI, DAVID; RAYMOND, JEFFERY R.; PETTIGREW, JEREMY D.
To: AQUINOX PHARMACEUTICALS INC.
Reel/Frame 036581/0040 →
CHANGE OF NAME Recorded Sep 16, 2015
From: AQUINOX PHARMACEUTICALS INC.
To: AQUINOX PHARMACEUTICALS (CANADA) INC.
Reel/Frame 036619/0679 →
Continuity (3)
Provisional Application 61785860 · Mar 14, 2013
Related Publication 20160083387A1 · Mar 24, 2016
Related Publication 20170253596A2 · Sep 7, 2017