IP Library Granted Patent US 10,766,906
Granted Patent B2
US 10,766,906 · App. 16/086,414 · Granted Sep 8, 2020

Fused hexacyclic imidazole derivatives as modulators of TNF activity

Inventors: Teresa De Haro Garcia (Slough, GB); Michael Louis Robert Deligny (Brussels, BE); Jag Paul Heer (Slough, GB); Helen Tracey Horsley (Slough, GB); Sophie Jadot (Brussels, BE); Jean Keyaerts (Brussels, BE)
Assignee: UCB Biopharma SRL
C07D487/22C07D487/04C07D487/18
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Quick Facts
Patent No.
US 10,766,906
App. No.
16/086,414
Granted
Sep 8, 2020
Kind
B2
Abstract

Disclosed are substituted fused hexacyclic benzimidazole derivatives of Formula (I) wherein the variables A, B, D, X, M, Q, n, p, q, Z, E, R 5 , and R 12 are defined herein. These compounds are potent modulators of human TNFα activity and of benefit in the treatment and/or prevention of various human ailments, including autoimmune and inflammatory disorders; neurological and neurodegenerative disorders; pain and nociceptive disorders; cardiovascular disorders; metabolic disorders; ocular disorders; and oncological disorders.

Claims (45)

1. A compound of formula (I) or an N-oxide thereof, or a pharmaceutically acceptable salt thereof:

wherein

A represents C—R 6 ;

B represents C—R 7 ;

D represents C—R 8 ;

—(X-M-Q)- represents an optionally substituted five-membered heteroaromatic ring selected from pyrrolyl, pyrazolyl, imidazolyl, triazolyl and tetrazolyl optionally substituted by one, two or three substituents selected from C 1-6 alkyl, trifluoromethyl, hydroxy and oxo;

Z represents methylene;

E represents a fused heteroaromatic ring system of formula (Ea)

wherein the asterisks (*) represent the site of attachment of E to the remainder of the molecule;

R 1 represents chloro; or R 1 represents pyrimidinyl, cyclobutylpyridinyl, cyclopentylpyridinyl, cyclobutylpyrimidinyl, azetidinylpyrimidinyl or piperazinyl-pyrimidinyl, any of which groups may be optionally substituted by one two or three substituents independently selected from halogen, trifluoromethyl, hydroxy, hydroxy(C 1-6 )alkyl, oxo, amino and amino(C 1-6 )alkyl;

R 2 represents hydrogen or halogen;

R 3 and R 4 independently represent hydrogen, halogen or or C 1-6 alkyl;

R 5 represents difluoro-methoxy or methoxy;

R 6 represents hydrogen, halogen or trifluoromethyl;

R 7 represents hydrogen or trifluoromethyl;

R 8 represents hydrogen or trifluoromethyl; and

R 12 represents hydrogen or C 1-6 alkyl.

2. The compound as claimed in claim 1 represented by formula (IIA) or an N-oxide thereof, or a pharmaceutically acceptable salt thereof:

wherein —(X-M-Q)-, R 1 , R 2 , R 5 , R 6 , R 7 and R 8 are as defined in claim 1 .

3. The compound as claimed in claim 2 represented by formula (IIA-1) or an N-oxide thereof, or a pharmaceutically acceptable salt thereof:

wherein

W represents N, CH or CF;

R 9 represents hydroxy(C 1-6 )alkyl or amino(C 1-6 )alkyl;

R 10 represents hydrogen or C 1-6 alkyl.

4. The compound as claimed in claim 1 selected from

2-{5-[(8R,15R)-7-(Difluoromethoxy)-8H,15H-8,15-methanobenzimidazo[2,1-d]imidazo-[2,1-a][2,5]benzodiazocin-11-yl]pyrimidin-2-yl}propan-2-ol;

2-{5-[(8R,15R)-7-(Difluoromethoxy)-1-methyl-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,4]triazolo[3,4-a][2,5]benzodiazocin-11-yl]pyrimidin-2-yl}propan-2-ol;

2-{5-[(8R,15R)-7-(Difluoromethoxy)-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,4]-triazolo[3,4-a][2,5]benzodiazocin-11-yl]pyrimidin-2-yl}propan-2-ol;

2-{5-[(8R,15R)-12-Chloro-7-(difluoromethoxy)-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,4]triazolo[3,4-a][2,5]benzodiazocin-11-yl]pyrimidin-2-yl}propan-2-ol;

(8R,15R)-7-(Difluoromethoxy)-11-[2-(2-hydroxypropan-2-yl)pyrimidin-5-yl]-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,4]triazolo[3,4-a][2,5]-benzodiazocin-1-ol;

(8R,15R)-11-Chloro-7-(difluoromethoxy)-8H,15H-8,15-methanobenzimidazo[2,1-d]-[1,2,3]triazolo[5,1-a][2,5]benzodiazocine;

2-{5-[(8R,15R)-7-(Difluoromethoxy)-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,3]-triazolo[5,1-a][2,5]benzodiazocin-11-yl]pyrimidin-2-yl}propan-2-ol;

(8R,15R)-11-Chloro-7-(difluoromethoxy)-1-methyl-8H,15H-8,15-methanobenzimidazo-[2,1-d]imidazo[5,1-a][2,5]benzodiazocine;

2-{5-[(8R,15R)-7-(Difluoromethoxy)-1-methyl-8H,15H-8,15-methanobenzimidazo[2,1-d]imidazo[5,1-a][2,5]benzodiazocin-11-yl]pyrimidin-2-yl}propan-2-ol;

2-{5-[(8R,15S)-7-(Difluoromethoxy)-2-methyl-8,15-dihydro-3H-8,15-methanobenzimidazo[1,2-b]imidazo[4,5-e][2]benzazocin-11-yl]pyrimidin-2-yl}propan-2-ol;

2-{5-[(8R,15R)-7-(Difluoromethoxy)-1-(trifluoromethyl)-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,4]triazolo[3,4-a][2,5]benzodiazocin-11-yl]pyrimidin-2-yl}-propan-2-ol;

2-{5-[(8R,15R)-7-(Difluoromethoxy)-1-methyl-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,4]triazolo[3,4-a][2,5]benzodiazocin-11-yl]pyrimidin-2-yl}propan-2-amine;

1-{5-[(8R,15R)-7-(Difluoromethoxy)-1-methyl-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,4]triazolo[3,4-a][2,5]benzodiazocin-11-yl]pyrimidin-2-yl}cyclobutanamine;

1-{5-[(8R,15R)-7-(Difluoromethoxy)-12-fluoro-1-methyl-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,4]triazolo[3,4-a][2,5]benzodiazocin-11-yl]-3-fluoropyridin-2-yl}-cyclopentanamine hydrochloride;

1-{5-[(8R,15R)-7-(Difluoromethoxy)-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,3]-triazolo[5,1-a][2,5]benzodiazocin-11-yl]-3-fluoropyridin-2-yl}cyclobutanamine hydrochloride;

1-{5-[(8R,15R)-7-(Difluoromethoxy)-1-methyl-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,4]triazolo[3,4-a][2,5]benzodiazocin-11-yl]pyrimidin-2-yl}-3-(trifluoromethyl)-azetidin-3-ol;

1-{5-[(8R,15R)-7-(Difluoromethoxy)-1-methyl-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,4]triazolo[3,4-a][2,5]benzodiazocin-11-yl]-3-fluoropyridin-2-yl}cyclobutanamine;

1-{5-[(8R,15R)-7-(Difluoromethoxy)-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,4]-triazolo[3,4-a][2,5]benzodiazocin-11-yl]-3-fluoropyridin-2-yl}cyclobutanamine; and

4-{5-[(8R,15R)-7-(Difluoromethoxy)-1-methyl-8H,15H-8,15-methanobenzimidazo[2,1-d][1,2,4]triazolo[3,4-a][2,5]benzodiazocin-11-yl]pyrimidin-2-yl}piperazin-2-one.

5. A pharmaceutical composition comprising a compound of formula (I) as defined in claim 1 or an N-oxide thereof, or a pharmaceutically acceptable salt thereof, in association with a pharmaceutically acceptable carrier.

Assignments (7)
CHANGE OF NAME Recorded Jul 22, 2020
From: UCB BIOPHARMA SPRL
To: UCB BIOPHARMA SRL
Reel/Frame 053283/0693 →
ASSIGNMENT OF UNDIVIDED INTEREST Recorded Sep 12, 2019
From: UCB BIOPHARMA SPRL
To: SANOFI; UCB BIOPHARMA SPRL
Reel/Frame 050355/0803 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2019
From: CELLTECH R&D LIMITED
To: UCB S.A.
Reel/Frame 049652/0053 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2019
From: UCB PHARMA S.A.
To: UCB BIOPHARMA SPRL
Reel/Frame 049652/0442 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2019
From: DELIGNY, MICHAEL LOUIS ROBERT; KEYAERTS, JEAN; HEER, JAG PAUL; JADOT, SOPHIE
To: UCB BIOPHARMA SPRL
Reel/Frame 049652/0486 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2019
From: UCB S.A.
To: UCB PHARMA S.A.
Reel/Frame 049652/0071 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2019
From: GARCIA, TERESA DE HARO; HORSLEY, HELEN TRACEY
To: CELLTECH R&D LIMITED
Reel/Frame 049651/0988 →
Priority Claims (1)
EP 16163577 · Apr 1, 2016 · regional
Continuity (1)
Related Publication 20190100526A1 · Apr 4, 2019