IP Library Granted Patent US 10,202,405
Granted Patent B2
US 10,202,405 · App. 15/513,357 · Granted Feb 12, 2019

Fused pentacyclic imidazole derivatives

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Quick Facts
Patent No.
US 10,202,405
App. No.
15/513,357
Granted
Feb 12, 2019
Kind
B2
Abstract

A series of fused pentacyclic imidazole derivatives, being potent modulators of human TNFa activity, are accordingly 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. In particular, the present invention is concerned with 6,7-dihydro-7,14-methanobenzimidazo[1,2-b][2,5]benzodiazocin-5(14H)-one derivatives and analogs thereof.

Claims (53)

1. A compound represented by formula (IB), or an N-oxide thereof, or a pharmaceutically acceptable salt thereof,

—X-Q- represents —O—, —O—C(O)—, —O—C(CH—CN)—, —S—, —SO—, —SO 2 —; or —N(R g )—, —N(R f )—CO—, —N(R f )—SO 2 —, O—CH 2 —, —CH 2 —S—, —CH 2 —SO—, —CH 2 —SO 2 —, —N(R g )—CH 2 —, —N(R f )—C(S)—, —N═S(O)(CH 3 )—, —O—C(═CH 2 )— or —S(═N—CN)—, any of which groups may be optionally substituted by one or more substituents selected from fluoro, methyl, carboxy, trifluoromethyl, methylcarbonyl, deuterated methyl, ethoxycarbonyl, hydroxyisopropyl, and hydroxymethyl;

R 1 represents halogen or cyano; or aryl, heteroaryl, (C 3-7 )cycloalkyl-heteroaryl, (C 3-7 )heterocycloalkyl-heteroaryl, (C 4-9 )heterobicycloalkyl-heteroaryl, (C 3-7 )heterocycloalkyl, (C 3-7 )heterocycloalkenyl, or (C 3-7 )heterocycloalkenyl-aryl, any of which groups may be optionally substituted by one or more substituents selected from halogen, cyano, cyano(C 1-6 )alkyl, C 1-6 alkyl, difluoromethyl, trifluoromethyl, hydroxy, (hydroxy)(C 1-6 )alkyl, amino, (amino)(C 1-6 ) alkyl, C 1-6 alkoxy, (C 1-6 ) alkoxy(C 1-6 )alkyl, C 2-6 alkylcarbonyl, C 2-6 alkoxycarbonyl, (C 2-6 ) alkoxycarbonyl-amino-C 1-6 alkyl, phosphate(C 1-6 )alkyl, C 1-6 alkylthio, C 1-6 alkylsulphonyl, oxo, (C 1-6 )alkylsulphoximinyl, (C 1-6 )alkylsulphinyl-amino-, di(C 1-6 )alkylamino (C 1-6 )alkyl, (C 2-6 )alkylcarbonylamino(C 1-6 )alkyl, di(C 1-6 )alkenylamino (C 1-6 )alkyl, (C 2-6 )alkylcarbonylamino(C 1-6 )alkyl, C 1-6 alkylsulphonyl-amino-C 1-6 alkyl, tetrahydrofuranyl, sulphate(C 1-6 )alkyl, and carboxy-(C 1-6 )alkyl-carbonyloxy-(C 1-6 )alkyl;

R 2 represents hydrogen or halogen;

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

R 5 represents halogen, —OR a , difluoromethoxy or trifluoromethoxy;

R 6 represents hydrogen, halogen or trifluoromethyl;

R 7 represents hydrogen or trifluoromethyl;

R 8 represents hydrogen, halogen or trifluoromethyl;

R a represents C 1-6 alkyl;

R f represents hydrogen; or C 1-6 alkyl, which group may be optionally substituted by one or more substituents selected from halogen or C 1-6 alkyl; and

R g represents hydrogen; or C 1-6 alkyl, —CO—(C 1-6 )alkyl, —SO 2 —(C 1-6 )alkyl —CO—(C 3-7 )heterocycloalkyl, —SO 2 —(C 3-7 )cycloalkyl, —SO 2 -aryl, —SO 2 -heteroaryl, heteroaryl or (C 2-6 )alkoxycarbonyl, any of which groups may be optionally substituted by one or more substituents selected from halogen or C 1-6 alkyl.

2. A compound represented by formula (IC), or an N-oxide thereof, or a pharmaceutically acceptable salt thereof,

—X-Q- represents —O—, —O—C(O)—, —O—C(CH—CN)—, —S—, —SO—, —SO 2 —; or —N(R g )—, —N(R f )—CO—, —N(R f )—SO 2 —, O—CH 2 —, —CH 2 —S—, —CH 2 —SO—, —CH 2 —SO 2 —, —N(R g )—CH 2 —, —N(R f )—C(S)—, —N═S(O)(CH 3 )—, —O—C(═CH 2 )— or —S(═N—CN)—, any of which groups may be optionally substituted by one or more substituents selected from fluoro, methyl, carboxy, trifluoromethyl, methylcarbonyl, deuterated methyl, ethoxycarbonyl, hydroxyisopropyl, and hydroxymethyl;

R 1 represents halogen or cyano; or aryl, heteroaryl, (C 3-7 )cycloalkyl-heteroaryl, (C 3-7 )heterocycloalkyl-heteroaryl, (C 4-9 )heterobicycloalkyl-heteroaryl, (C 3-7 )heterocycloalkyl, (C 3-7 )heterocycloalkenyl, or (C 3-7 )heterocycloalkenyl-aryl, any of which groups may be optionally substituted by one or more substituents selected from halogen, cyano, cyano(C 1-6 )alkyl, C 1-6 alkyl, difluoromethyl, trifluoromethyl, hydroxy, (hydroxy)(C 1-6 )alkyl, amino, (amino)(C 1-6 ) alkyl, C 1-6 alkoxy, (C 1-6 ) alkoxy(C 1-6 )alkyl, C 2-6 alkylcarbonyl, C 2-6 alkoxycarbonyl, (C 2-6 ) alkoxycarbonyl-amino-C 1-6 alkyl, phosphate(C 1-6 )alkyl, C 1-6 alkylthio, C 1-6 alkylsulphonyl, oxo, (C 1-6 )alkylsulphoximinyl, (C 1-6 )alkylsulphinyl-amino-, di(C 1-6 )alkylamino (C 1-6 )alkyl, (C 2-6 )alkylcarbonylamino(C 1-6 )alkyl, di(C 1-6 )alkenylamino (C 1-6 )alkyl, (C 2-6 )alkylcarbonylamino(C 1-6 )alkyl, C 1-6 alkylsulphonyl-amino-C 1-6 alkyl, tetrahydrofuranyl, sulphate(C 1-6 )alkyl, and carboxy-(C 1-6 )alkyl-carbonyloxy-(C 1-6 )alkyl;

R 2 represents hydrogen or halogen;

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

R 5 represents halogen, —OR a , difluoromethoxy or trifluoromethoxy;

R 6 represents hydrogen, halogen or trifluoromethyl;

R 7 represents hydrogen or trifluoromethyl;

R 8 represents hydrogen, halogen or trifluoromethyl;

R a represents C 1-6 alkyl;

R f represents hydrogen; or C 1-6 alkyl, which group may be optionally substituted by one or more substituents selected from halogen or C 1-6 alkyl; and

R g represents hydrogen; or C 1-6 alkyl, —CO—(C 1-6 )alkyl, —SO 2 —(C 1-6 )alkyl —CO—(C 3-7 )heterocycloalkyl, —SO 2 —(C 3-7 )cycloalkyl, —SO 2 -aryl, —SO 2 -heteroaryl, heteroaryl or (C 2-6 )alkoxycarbonyl, any of which groups may be optionally substituted by one or more substituents selected from halogen or C 1-6 alkyl.

3. A compound as claimed in claim 1 wherein —X-Q- include —O—, —O—CO—, —O—C(CH—CN)—, —S—, —SO—, SO 2 —, —NH—, —N(CO—CH 3 )—, —N(SO 2 —CH 3 )—, —N(CH 2 —CO—O—CH 2 —CH 3 )—, —N[(CO—CH 2 -(3,7-dioxa-9-azabicyclo[3.3.1]non-9-yl)]-, —N[CO— (azetidin-3-yl)]-, —N[CO-(methylsulphonyl)azetidin-3-yl)]-, —N(CH 2 —COOH), —N[(tert-butyl)(dimethyl)silyloxyethyl]-, —N(SO 2 -pyridine-3-yl)-, —N—(SO 2 -cyclopropyl)-, —N(CH 3 )—CH 2 —, —N(CH 2 —CH 2 —OH)—, —N(SO 2 -phenyl)-, —N[SO 2 -(6-methoxy-pyridin-3-yl)]-, —NH—CO—, —N(CH 3 )—CO—, —N(CH 2 CH 3 )—CO—, —N(CH(CH 3 ) 2 )—CO—, —N(CH 2 —COOH)—CO—, —N(CH 2 —CF 3 )—CO—, —N(CH 2 —CH 2 —OH)—CO—, —N(CH 2 —C(OH)(CH 3 ) 2 )—CO—, —N(CD 3 )-CO—, —NH—CH 2 —, —N(CH 2 —COOH)—CH 2 —, —NH—CH(CF 3 )—, —NH—CH(CH 3 )—, —NH—C(S)—, —N(CO—CH 3 )—CH(CH 3 )—, —N(SO 2 —CH 3 )—CH 2 —, —N(CO—CH 3 )—CH(CH 3 )—, —N═S(O)(CH 3 )—, O—CH(CF 3 )—, —CH(COOC 2 H 5 )—S—, —CH 2 —S(O)—, —CH 2 —S(O) 2 —, —CH(CH(OH)(CH 3 ) 2 )—S—, —CH(CH 2 OH)—S—, —O—C(═CH 2 )—, —N[S(O) 2 -(pyridin-1H-2-one)], —NH—S(O) 2 —, —N(pyrimidinyl)-, —N(COOC 2 H 5 )—, —S(═N—CN)—, —N(SO 2 —CH 3 )— or —N(C 2 H 5 )—CO—.

4. A compound as claimed in claim 1 wherein —X-Q- represents represents —N(R f )—C(O)—.

5. A compound of formula (IIB) or an N-oxide thereof, or a pharmaceutical acceptable salt thereof,

wherein

R 1 represents halogen or cyano; or aryl, heteroaryl, (C 3-7 )cycloalkyl-heteroaryl, (C 3-7 )heterocycloalkyl-heteroaryl, (C 4-9 )heterobicycloalkyl-heteroaryl, (C 3-7 )heterocycloalkyl, (C 3-7 )heterocycloalkenyl, or (C 3-7 )heterocycloalkenyl-aryl, any of which groups may be optionally substituted by one or more substituents selected from halogen, cyano, cyano(C 1-6 )alkyl, C 1-6 alkyl, difluoromethyl, trifluoromethyl, hydroxy, (hydroxy)(C 1-6 )alkyl, amino, (amino)(C 1-6 ) alkyl, C 1-6 alkoxy, (C 1-6 ) alkoxy(C 1-6 )alkyl, C 2-6 alkylcarbonyl, C 2-6 alkoxycarbonyl, (C 2-6 ) alkoxycarbonyl-amino-C 1-6 alkyl, phosphate(C 1-6 )alkyl, C 1-6 alkylthio, C 1-6 alkylsulphonyl, oxo, (C 1-6 )alkylsulphoximinyl, (C 1-6 )alkylsulphinyl-amino-, di(C 1-6 )alkylamino (C 1-6 )alkyl, (C 2-6 )alkylcarbonylamino(C 1-6 )alkyl, di(C 1-6 )alkenylamino (C 1-6 )alkyl, (C 2-6 )alkylcarbonylamino(C 1-6 )alkyl, C 1-6 alkylsulphonyl-amino-C 1-6 alkyl, tetrahydrofuranyl, sulphate(C 1-6 )alkyl, and carboxy-(C 1-6 )alkyl-carbonyloxy-(C 1-6 )alkyl;

R 2 represents hydrogen or halogen;

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

R 5 represents halogen, —OR a , difluoromethoxy or trifluoromethoxy;

R 6 represents hydrogen, halogen or trifluoromethyl;

R 7 represents hydrogen or trifluoromethyl;

R 8 represents hydrogen, halogen or trifluoromethyl;

R a represents C 1-6 alkyl; and

R f represents hydrogen; or C 1-6 alkyl, which group may be optionally substituted by one or more substituents selected from halogen or C 1-6 alkyl.

6. A compound as claimed in claim 1 represented by formula (IIB-A), or an N-oxide thereof, or a pharmaceutically acceptable salt thereof,

wherein

R 1 represents aryl or heteroaryl, either of which groups may be optionally substituted by one or more substituents selected from halogen, cyano, cyano(C 1-6 )alkyl, C 1-6 alkyl, difluoromethyl, trifluoromethyl, hydroxy, (hydroxy)(C 1-6 )alkyl, amino, (amino)(C 1-6 ) alkyl, C 1-6 alkoxy, (C 1-6 ) alkoxy(C 1-6 )alkyl, C 2-6 alkylcarbonyl, C 2-6 alkoxycarbonyl, (C 2-6 ) alkoxycarbonyl-amino-C 1-6 alkyl, phosphate(C 1-6 )alkyl, C 1-6 alkylthio, C 1-6 alkylsulphonyl, oxo, (C 1-6 )alkylsulphoximinyl, (C 1-6 )alkylsulphinyl-amino-, di(C 1-6 )alkylamino (C 1-6 )alkyl, (C 2-6 )alkylcarbonylamino(C 1-6 )alkyl, di(C 1-6 )alkenylamino-(C 1-6 )alkyl, (C 2-6 )alkylcarbonylamino(C 1-6 )alkyl, C 1-6 alkylsulphonyl-amino-C 1-6 alkyl, tetrahydrofuranyl, sulphate(C 1-6 )alkyl, and carboxy-(C 1-6 )alkyl-carbonyloxy-(C 1-6 )alkyl.

7. A compound as claimed in claim 6 represented by formula (IIB-AB-A), an N-oxide thereof, or pharmaceutically acceptable salt thereof,

wherein

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

R 10 represents hydrogen or C 1-6 alkyl;

and

W represents N or C—H.

8. A compound as claimed in claim 7 wherein W represents N; and/or R 10 represents hydrogen.

9. A compound as claimed in claim 7 wherein R 9 represents 2-hydroxy-prop-2-yl.

10. A compound as claimed in claim 5 wherein

(i) R 2 represents fluoro; and/or

(ii) R 5 represents difluoromethoxy; and/or

(iii) R f represents hydrogen.

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

Assignments (14)
CHANGE OF ADDRESS Recorded Jul 3, 2024
From: SANOFI
To: SANOFI
Reel/Frame 068105/0767 →
CHANGE OF NAME Recorded Mar 31, 2020
From: UCB BIOPHARMA SPRL
To: UCB BIOPHARMA SRL
Reel/Frame 052279/0642 →
ASSIGNMENT OF UNDIVIDED INTEREST Recorded Sep 12, 2019
From: UCB BIOPHARMA SPRL
To: SANOFI; UCB BIOPHARMA SPRL
Reel/Frame 050355/0895 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2019
From: DE HARO GARCIA, TERESA; QUINCEY, JOANNA RACHEL; XUAN, MENGYANG; ZHU, ZHAONING; BROOKINGS, DANIEL CHRISTOPHER; CALMIANO, MARK DANIEL; HUTCHINGS, MARTIN CLIVE; SELBY, MATTHEW DUNCAN; SHAW, MICHAEL ALAN; JOHNSON, JAMES ANDREW
To: CELLTECH R&D LIMITED
Reel/Frame 049062/0475 →
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY PREVIOUSLY RECORDED AT REEL: 043450 FRAME: 0395. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Feb 6, 2019
From: HEER, JAG PAUL
To: CELLTECH R&D LIMITED; UCB BIOPHARMA SPRL
Reel/Frame 048264/0358 →
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY TO NOW BE CELLTECH R&D LIMITED PREVIOUSLY RECORDED ON REEL 043450 FRAME 0395. ASSIGNOR(S) HEREBY CONFIRMS THE RECEIVING PARTY TO NOW BE CELLTECH R&D LIMITED. Recorded Feb 1, 2019
From: QUINCEY, JOANNA RACHEL
To: CELLTECH R&D LIMITED
Reel/Frame 048207/0725 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 21, 2018
From: CELLTECH R&D LIMITED
To: UCB SA
Reel/Frame 047842/0791 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 21, 2018
From: UCB PHARMA SA
To: UCB BIOPHARMA SPRL
Reel/Frame 047842/0863 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 21, 2018
From: BOHICKET PHARMA CONSULTING LLC
To: UCB PHARMA SA
Reel/Frame 047842/0899 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 21, 2018
From: UCB SA
To: UCB PHARMA SA
Reel/Frame 047842/0818 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2017
From: MAC COSS, MALCOLM
To: BOHICKET PHARMA CONSULTING LLC
Reel/Frame 043450/0220 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2017
From: GARCIA, TERESA DE HARO; HEER, JAG PAUL; QUINCEY, JOANNA RACHEL; XUAN, MENGYANG; ZHU, ZHOANING; BROOKINGS, DANIEL CHRISTOPHER; CALMIANO, MARK DANIEL; HUTCHINGS, MARTIN CLIVE; JOHNSON, JAMES ANDREW; SELBY, MATTHEW DUNCAN; SHAW, MICHAEL ALAN
To: UCB CELLTECH
Reel/Frame 043450/0395 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2017
From: DELIGNY, MICHAEL; EVRARD, YVES; JADOT, SOPHIE; KEYAERTS, JEAN; SWINNEN, DOMINIQUE LOUIS LEON
To: UCB BIOPHARMA SPRL
Reel/Frame 043450/0412 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 15, 2017
From: SCHIO, LAURENT; FORICHER, YANN; FILOCHE-ROMME, BRUNO
To: SANOFI
Reel/Frame 042374/0444 →