IP Library Granted Patent US 11,845,725
Granted Patent B2
US 11,845,725 · App. 17/946,587 · Granted Dec 19, 2023

Antibacterial compounds

Inventors: Ian Cooper (Macclesfield, GB); David Orr (Macclesfield, GB); Andrew Wilkinson (Macclesfield, GB); Jonathan Finlayson (Macclesfield, GB); Adam Bunt (Macclesfield, GB); Pia Appelqvist (Trosa, SE); Hans Wallberg (Huddinge, SE); Fredrik Wångsell (Mölndal, SE)
Assignee: INFEX Therapeutics Limited
C07D207/48A61P31/04C07D207/36C07D401/04C07D401/10C07D401/12C07D401/14C07D403/04C07D403/12C07D403/14C07D417/04C07D487/04
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Quick Facts
Patent No.
US 11,845,725
App. No.
17/946,587
Granted
Dec 19, 2023
Kind
B2
Abstract

This invention relates to compounds of formula (I) and methods of treatment using the compounds. The compounds of the invention can be used in combination with antibacterial agents to treat bacterial infections. More specifically, the compounds of formula (I) can be used in combination with a class of antibacterial agents known as carbapenems. The novel compounds of the present invention are enzyme inhibitors and more particularly are metallo-β-lactamase inhibitors.

Claims (28)

1. A compound of formula (IV) or a pharmaceutically acceptable salt, or hydrate thereof:

wherein

R 1 is selected from:

R 2 is —C(O)OH or —C(O)OM; wherein M is a group 1 cation;

R 3 is selected as appropriate to satisfy valence requirements from the group consisting of: C 1-6 alkyl, C 1-6 alkoxy, C 2-6 alkenyl, C 2-6 alkynyl, C 3-8 cycloalkyl, —(CH 2 ) d -aryl, —(CH 2 ) d -heteroaryl, —(CH 2 ) e -heterocyclyl, —OR 5 , —N(R 5 ) 2 , —SO 2 R 5 , —SO 2 N(R 5 ) 2 , —NHSO 2 R 7 , —NHCOR 5 , —CON(R 5 ) 2 and —COR 5 , wherein each of the C 1-6 alkyl, C 1-6 alkoxy, C 2-6 alkenyl, C 2-6 alkynyl, C 3-8 cycloalkyl, —(CH 2 ) d -aryl, —(CH 2 ) d -heteroaryl, —(CH 2 ) e -heterocyclyl, —OR 5 , —N(R 5 ) 2 , —SO 2 R 5 , —SO 2 N(R 5 ) 2 , —NHSO 2 R 7 , —NHCOR 5 , —CON(R 5 ) 2 and —COR 5 substituents may themselves be optionally substituted where chemically possible with one, two or three groups independently selected at each occurrence from the group consisting of: halo, —N(R 5 ) 2 , —OH, —C(═O)C 1-6 alkyl, —SO 2 N(C 1-6 alkyl) 2 , —(CH 2 ) h OR 5 , C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-8 cycloalkyl, and C 3-8 cycloalkenyl;

R 4 is selected at each occurrence from the group consisting of: H, halo, substituted or unsubstituted C 1-6 alkyl, and substituted or unsubstituted C 3-8 cycloalkyl;

R 5 is independently selected at each occurrence from the group consisting of: H, halo, —OH, C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-8 cycloalkyl, C 3-8 cycloalkenyl, —(CH 2 ) f -aryl, —(CH 2 ) d -heteroaryl, and —(CH 2 ) g -heterocyclyl;

wherein each of R 4 and R 5 may themselves be optionally substituted where chemically possible with one, two or three groups independently selected at each occurrence from the group consisting of: halo, —NH 2 , —N(C 1-4 alkyl) 2 , —OH, —SO 2 N(C 1-4 alkyl) 2 , —NHC(═O)OC 1-6 alkyl, and —C(═O)OC 1-6 alkyl;

R 7 is selected from the group consisting of: H, C 1-4 alkyl, C 1-4 alkyl amine, C 3-8 cycloalkyl and C 6-10 aryl, and 5 to 10 membered heteroaryl;

d, e, f, g and h are independently selected from integers 0 to 3; and

n is an integer selected from: 0 to 2.

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

3. A compound according to claim 1 , wherein R 1 is

4. A compound according to claim 1 , wherein R 2 is C(O)OH.

5. A compound according to claim 1 , wherein R 2 is C(O)OM.

6. A compound as claimed in claim 1 , wherein R 3 is selected as appropriate to satisfy valence requirements from the group consisting of: C 1-6 alkyl, C 1-6 alkoxy, 3 to 10 membered heterocyclyl, —OR 5 , —N(R 5 ) 2 , —SO 2 R 5 , —SO 2 N(R 5 ) 2 , —NHSO 2 R 7 , —CON(R 5 ) 2 and —COR 5 wherein each of the C 1-6 alkyl, C 1-6 alkoxy, 3 to 10 membered heterocyclyl, —OR 5 , —N(R 5 ) 2 , —SO 2 R 5 , —SO 2 N(R 5 ) 2 , —NHSO 2 R 7 , —CON(R 5 ) 2 and —COR 5 substituents may themselves be optionally substituted where chemically possible with one, two or three groups independently selected at each occurrence from the group consisting of: halo, C 1-6 alkyl, —C(═O)C 1-6 alkyl and —SO 2 N(C 1-6 alkyl) 2 .

7. A compound as claimed in claim 6 , wherein R 3 is a 3 to 10 membered heterocyclyl, wherein the 3 to 10 membered heterocyclyl substituent is optionally substituted where chemically possible with one, two or three groups independently selected at each occurrence from the group consisting of: halo, C 1-6 alkyl, —C(═O)C 1-6 alkyl and —SO 2 N(C 1-6 alkyl) 2 .

8. A compound as claimed in claim 6 , wherein R 3 is —SO 2 R 5 , wherein the —SO 2 R 5 substituent is optionally substituted where chemically possible with one, two or three groups independently selected at each occurrence from the group consisting of: halo, C 1-6 alkyl, —C(═O)C 1-6 alkyl and —SO 2 N(C 1-6 alkyl) 2 .

9. A compound as claimed in claim 6 , wherein R 3 is —SO 2 N(R 5 ) 2 , wherein the —SO 2 N(R 5 ) 2 substituent is optionally substituted where chemically possible with one, two or three groups independently selected at each occurrence from the group consisting of: halo, C 1-6 alkyl, —C(═O)C 1-6 alkyl and —SO 2 N(C 1-6 alkyl) 2 .

10. A compound as claimed in claim 6 , wherein R 3 is —CON(R 5 ) 2 , wherein the —CON(R 5 ) 2 substituent is optionally substituted where chemically possible with one, two or three groups independently selected at each occurrence from the group consisting of: halo, C 1-6 alkyl, —C(═O)C 1-6 alkyl and —SO 2 N(C 1-6 alkyl) 2 .

11. A compound as claimed in claim 1 , wherein R 4 is independently selected at each occurrence from H, fluoro and Me.

12. A compound as claimed in claim 1 , wherein R 5 is independently selected at each occurrence from the group consisting of: H, —OH, C 1-6 alkyl, C 1-6 haloalkyl, 3 to 10 membered heterocyclyl, and C 3-8 cycloalkyl; wherein each R 5 may themselves be optionally substituted where chemically possible with one or two groups independently selected at each occurrence from the group consisting of: —NH 2 , —OH, —SO 2 N(C 1-4 alkyl) 2 , —NHC(═O)Otert-butyl and —C(═O)Otert-butyl.

13. A compound as claimed in claim 1 , wherein the compound is selected from:

14. A pharmaceutical composition which comprises a compound of Formula (IV) as claimed in claim 1 , or a pharmaceutically acceptable salt, or hydrate thereof, in association with one or more pharmaceutically acceptable excipients.

15. A method for the treatment of bacterial infection in a patient in need of such treatment, said method comprising administering to said patient a therapeutically effective amount of a combination of an antibacterial agent and a compound of Formula (IV) as claimed in claim 1 , or a pharmaceutically acceptable salt, or hydrate thereof; or administering to said patient a therapeutically effective amount of an antibacterial agent in combination with a pharmaceutical composition as claimed in claim 14 , containing a compound of Formula (IV) or a pharmaceutically acceptable salt, or hydrate thereof.

16. The method of claim 15 , wherein the bacterial infection is selected from: pneumonia, respiratory tract infections, urinary tract infections, intra-abdominal infections, skin and soft tissue infections, bloodstream infections, septicaemia, intra- and post-partum infections, prosthetic joint infections, endocarditis, acute bacterial meningitis and febrile neutropenia.

17. The method of claim 16 , wherein the bacterial infection is selected from: community acquired pneumonia, nosocomial pneumonia (hospital-acquired/ventilator-acquired), respiratory tract infections associated with cystic fibrosis, non-cystic fibrosis bronchiectasis, COPD, urinary tract infection, intra-abdominal infections, skin and soft tissue infection, bacteraemia, septicaemia, intra- and post-partum infections, prosthetic joint infections, endocarditis, acute bacterial meningitis and febrile neutropenia.

18. The method of claim 17 , wherein the bacterial infection is selected from: community acquired pneumonia, nosocomial pneumonia (hospital-acquired/ventilator-acquired), respiratory tract infections associated with cystic fibrosis, non-cystic fibrosis bronchiectasis, COPD, urinary tract infection, intra-abdominal infections, skin and soft tissue infection, bacteremia and septicemia.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2023
From: WILKINSON, ANDREW; COOPER, IAN; ORR, DAVID; FINLAYSON, JONATHAN; BUNT, ADAM
To: INFEX THERAPEUTICS LIMITED
Reel/Frame 062678/0081 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2023
From: APPELQVIST, PIA; WALLBERG, HANS; WÅNGSELL, FREDRIK
To: MEDIVIR AB
Reel/Frame 062678/0099 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2023
From: MEDIVIR AB
To: AMR CENTRE LTD.
Reel/Frame 062678/0130 →
CHANGE OF NAME Recorded Feb 13, 2023
From: AMR CENTRE LTD.
To: INFEX THERAPEUTICS LIMITED
Reel/Frame 062678/0160 →
Priority Claims (2)
GB 1807966 · May 16, 2018 · national
GB 1905174 · Apr 11, 2019 · national
Continuity (2)
Continuation 17055506
Related Publication 20230060011A1 · Feb 23, 2023
Cited By (1)
US 12,606,524