IP Library Granted Patent US 9,493,457
Granted Patent B2
US 9,493,457 · App. 14/684,813 · Granted Nov 15, 2016

4,5,6,7-tetrahyroimidazo[4,5-c]pyridine compounds

Inventors: Edward Savory (Cambourne, GB); Michael Higginbottom (Caldecote, GB); Kathryn Oliver (Cambridge, GB); Viet-Anh Anne Horgan (Redhill, GB)
Assignee: Proximagen Limited
C07D471/04A61K31/437
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Quick Facts
Patent No.
US 9,493,457
App. No.
14/684,813
Granted
Nov 15, 2016
Kind
B2
Abstract

The present invention relates to compounds of formula (I), and their pharmaceutically acceptable salts, solvates, hydrates, geometrical isomers, tautomers, optical isomers or N-oxides, which are inhibitors of SSAO activity. The invention further relates to pharmaceutical compositions comprising these compounds and to the use of these compounds for the treatment of medical conditions wherein inhibition of SSAO activity is beneficial, such as inflammatory diseases and immune disorders.

Claims (63)

1. A compound of formula (I),

or a pharmaceutically acceptable salt, solvate, hydrate, geometrical isomer, tautomer, optical isomer or N-oxide thereof, wherein:

R 1 is selected from:

(a) hydrogen,

(b) C 1-6 -alkyl, and

(c) —NR 4A R 4B ;

R 2 is selected from:

(a) hydrogen,

(b) —C(O)OMe,

(c) —C(O)NH 2 , and

(d) —C(O)NHMe;

R 3 is selected from:

(a) C 1-6 -alkyl,

(b) halo-C 1-6 -alkyl,

(c) hydroxy-C 1-6 -alkyl,

(d) C 1-6 -alkoxy-C 1-6 -alkyl,

(e) halo-C 1-6 -alkoxy-C 1-6 -alkyl,

(f) N(R 4A R 4B )—C 1-6 -alkyl,

(g) C 6-10 -aryl-C 1-4 -alkyl,

(h) heteroaryl-C 1-4 -alkyl,

(i) C 6-10 -aryloxy-C 1-4 -alkyl,

(j) heteroaryloxy-C 1-4 -alkyl,

(k) C 3-8 -cycloalkyl,

(l) C 3-8 -cycloalkyl-C 1-4 -alkyl,

(m) heterocyclyl, and

(n) heterocyclyl-C 1-4 -alkyl,

wherein any aryl or heteroaryl residue is optionally substituted with one more substituents independently selected from halogen, hydroxy, cyano, nitro, CF 3 , C 1-4 -alkyl, C 1-4 -alkoxy and —NR 4A R 4B , and wherein any cycloalkyl or heterocyclyl residue is optionally substituted with one or more substituents independently selected from halogen, hydroxy, C 1-4 -alkyl, C 1-4 -alkoxy and —NR 4A R 4B ;

R 4A and R 4B are each independently selected from:

(a) hydrogen,

(b) C 1-6 -alkyl, and

(c) C 1-6 -acyl

provided that when R 1 and R 2 are hydrogen, then R 3 is not benzyl.

2. A compound according to claim 1 , wherein R 1 is H.

3. A compound according to claim 1 , wherein R 3 is selected from halo-C 1-2 -alkyl, halo-C 1-2 -alkoxy-C 1-2 -alkyl, di(C 1-2 -alkyl)amino-C 1-2 -alkyl, phenyl-C 1-2 -alkyl, phenoxy-C 1-2 -alkyl, C 5-6 -heteroaryl-C 1-2 -alkyl, C 5-6 -heteroaryloxy-C 1-2 -alkyl, heterocyclyl and heterocyclyl-C 1-2 -alkyl, and wherein any phenyl, heteroaryl or heterocyclyl residue is optionally substituted with one or two substituents independently selected from halogen and C 1-2 -alkyl.

4. A pharmaceutical formulation containing a compound according to claim 1 as active ingredient, in combination with a pharmaceutically acceptable diluent or carrier.

5. A compound of formula (I),

or a pharmaceutically acceptable salt, solvate, hydrate, geometrical isomer, tautomer, optical isomer or N-oxide thereof, wherein:

R 1 is selected from:

(a) hydrogen,

(b) C 1-6 -alkyl, and

(c) —NR 4A R 4B ;

R 2 is selected from:

(a) hydrogen,

(b) —C(O)OMe,

(c) —C(O)NH 2 , and

(d) —C(O)NHMe;

R 3 is selected from:

(a) halo-C 1-4 -alkyl,

(b) halo-C 1-4 -alkoxy-C 1-4 -alkyl,

(c) di(C 1-4 -alkyl)-amino-C 1-4 -alkyl,

(d) C 6-10 -aryl-C 1-4 -alkyl,

(e) C 6-10 -aryloxy-C 1-4 -alkyl,

(f) heteroaryl-C 1-4 -alkyl,

(g) heteroaryloxy-C 1-4 -alkyl, and

(h) heterocyclyl and heterocyclyl-C 1-4 -alkyl, wherein any aryl, heteroaryl or heterocyclyl residue is optionally substituted with one or two substituents independently selected from halogen and C 1-4 -alkyl; and

R 4A and R 4B are each independently selected from:

(d) hydrogen,

(e) C 1-6 -alkyl, and

(f) C 1-6 -acyl

provided that when R 1 and R 2 are hydrogen, then R 3 is not benzyl.

6. A compound according to claim 5 , wherein R 1 is H.

7. The compound according to claim 5 , wherein R 3 is 2,2,2-trichloroethyl, 2-chloro-2,2-difluoroethyl, 2,2,2-trifluoroethoxyethyl, dimethylaminoethyl, benzyl, pyridinylmethyl, pyrazinylmethyl, thiazolylmethyl, isoxazolylmethyl, phenoxyethyl, pyridinyloxyethyl, tetrahydrofuranyl, tetrahydrofuranylmethyl, pyrrolidinyl, pyrrolidinylmethyl or oxetanylmethyl, wherein any phenyl, heteroaryl or heterocyclyl residue is optionally monosubstituted with halogen or methyl.

8. A pharmaceutical formulation containing a compound according to claim 5 as active ingredient, in combination with a pharmaceutically acceptable diluent or carrier.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 15, 2022
From: BENEVOLENTAI CAMBRIDGE LIMITED
To: PROXIMAGEN, LLC
Reel/Frame 059265/0350 →
CHANGE OF ADDRESS Recorded Mar 22, 2019
From: BENEVOLENTAI CAMBRIDGE LIMITED
To: BENEVOLENTAI CAMBRIDGE LIMITED
Reel/Frame 048676/0176 →
CHANGE OF NAME Recorded Dec 17, 2018
From: PROXIMAGEN LIMITED
To: BENEVOLENTAI CAMBRIDGE LIMITED
Reel/Frame 047799/0165 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2015
From: SAVORY, EDWARD; HIGGINBOTTOM, MICHAEL; OLIVER, KATHRYN; HORGAN, VIET-ANH ANNE
To: PROXIMAGEN LIMITED
Reel/Frame 035394/0808 →
Continuity (5)
Continuation 14062969 · Oct 25, 2013
Continuation 13567146 · Aug 6, 2012
Division 13062318
Provisional Application 61106734 · Oct 20, 2008
Related Publication 20150218161A1 · Aug 6, 2015