IP Library › Granted Patent US 11,352,326
Granted Patent B2
US 11,352,326 · App. 16/461,255 · Granted Jun 7, 2022

Myeloperoxidase imaging agents

Inventors: John W. Chen (Newton, MA); Cuihua Wang (Cambridge, MA); Edmund J. Keliher (Topsfield, MA)
Assignee: The General Hospital Corporation
C07D209/20A61K49/0021A61K51/0446C07D209/14C07D495/04
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Quick Facts
Patent No.
US 11,352,326
App. No.
16/461,255
Granted
Jun 7, 2022
Kind
B2
Abstract

Provided herein are compounds useful as imaging agents. Exemplary compounds provided herein are useful as myeloperoxidase imaging agents using positron emission tomography or fluorescence imaging techniques. Methods for preparing the compounds provided herein and diagnostic methods using radiolabeled and unlabeled compounds are also provided.

Claims (47)

1. A compound of Formula I:

or a pharmaceutically acceptable salt thereof, wherein:

L 1 is selected from the group consisting of a bond, —C(O)—, —C(O)O—, —C(O)NR a1 —, —C(O)(C 1-6 alkylene)-, and —C(O)(C 1-6 alkyleneoxy)-;

R 1 is selected from the group consisting of H, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 haloalkyl, C 3-10 cycloalkyl, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl, wherein each C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 haloalkyl, C 3-10 cycloalkyl, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl is optionally substituted by 1, 2, 3, or 4 substituents independently selected from OH, halo, C 1-6 alkoxy, and C 1-6 haloalkyl;

L 2 is selected from the group consisting of —(C 1-6 alkylene)-(C 3-10 cycloalkylene)-, —(C 1-6 alkylene)-(C 6-10 arylene)-, —(C 1-6 alkylene)-(4-10 membered heterocycloalkylene)-, —(C 1-6 alkylene)-(5-10 membered heteroarylene)-, —C(O)—, —C(O)O—, —C(O)NR a2 —, —C(O)(C 1-6 alkylene)-, and —C(O)(C 1-6 alkyleneoxy)-;

R 2 is selected from the group consisting of C 1-6 alkoxy, C 3-10 cycloalkyl, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl, wherein each C 1-6 alkoxy, C 3-10 cycloalkyl, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl is optionally substituted by 1, 2, 3, or 4 substituents independently selected from OH, halo, C 1-6 alkoxy, and C 1-6 haloalkyl;

L 3 is selected from the group consisting of a bond, —C(O)—, —C(O)O—, —C(O)(C 1-6 alkylene)-, —C(O)(C 1-6 alkyleneoxy)-, —C(O)N(R a3 )(C 1-6 alkylene)-, —C(O)N(R a3 )(C 1-6 alkylene)-di(C 1-6 alkyl)amino, and —C(O)N(R a3 )(C 1-6 alkyleneoxy)-;

R 3 is selected from the group consisting of C 1-6 haloalkyl, C 3-10 cycloalkyl, C 6-10 aryl, 4-10 membered heterocycloalkyl, 5-10 membered heteroaryl, and —C(O)N(R a3 )(C 1-6 haloalkoxy), wherein each C 1-6 haloalkyl, C 3-10 cycloalkyl, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl is optionally substituted by 1, 2, 3, or 4 substituents independently selected from OH, halo, and C 1-6 haloalkyl;

R 4 is H;

and each R a1 , R a2 , and R a3 is independently selected from the group consisting of H, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, and C 1-6 haloalkyl.

2. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein L 1 is selected from the group consisting of a bond, —C(O)—, —C(O)(C 1-6 alkylene)-, and —C(O)(C 1-6 alkyleneoxy)-.

3. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein L 1 is selected from the group consisting of a bond and —C(O)(C 1-6 alkylene)-.

4. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1 is selected from the group consisting of H, C 3-10 cycloalkyl, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl, wherein each C 1-6 alkyl, C 3-10 cycloalkyl, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl is optionally substituted by 1, 2, 3, or 4 substituents independently selected from OH, halo, and C 1-6 haloalkyl.

5. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein L 2 is selected from the group consisting of —(C 1-6 alkylene)-(C 3-10 cycloalkylene)-, —(C 1-6 alkylene)-(C 6-10 arylene)-, —(C 1-6 alkylene)-(4-10 membered heterocycloalkylene)-, —(C 1-6 alkylene)-(5-10 membered heteroarylene)-, —C(O)—, and —C(O)(C 1-6 alkylene)-.

6. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 2 is selected from the group consisting of C 1-6 alkoxy, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl, wherein each C 1-6 alkoxy, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl is optionally substituted by 1, 2, 3, or 4 substituents independently selected from OH, halo, and C 1-6 haloalkyl.

7. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein L 3 is selected from the group consisting of a bond, —C(O)N(R a3 )(C 1-6 alkylene)-, —C(O)N(R a3 )(C 1-6 alkylene)-di(C 1-6 alkyl)amino, and —C(O)N(R a3 )(C 1-6 alkyleneoxy)-.

8. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein each R a1 , R a2 and R a3 is H.

9. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein:

L 1 is selected from the group consisting of a bond, —C(O)—, —C(O)(C 1-6 alkylene)-, and —C(O)(C 1-6 alkyleneoxy)-;

R 1 is selected from the group consisting of H, C 3-10 cycloalkyl, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl, wherein each C 1-6 alkyl, C 3-10 cycloalkyl, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl is optionally substituted by 1, 2, 3, or 4 substituents independently selected from OH, halo, and C 1-6 haloalkyl;

L 2 is selected from the group consisting of —(C 1-6 alkylene)-(C 3-10 cycloalkylene)-, —(C 1-6 alkylene)-(C 6-10 arylene)-, —(C 1-6 alkylene)-(4-10 membered heterocycloalkylene)-, —(C 1-6 alkylene)-(5-10 membered heteroarylene)-, —C(O)—, and —C(O)(C 1-6 alkylene)-;

R 2 is selected from the group consisting of C 1-6 alkoxy, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl, wherein each C 1-6 alkoxy, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl is optionally substituted by 1, 2, 3, or 4 substituents independently selected from OH, halo, and C 1-6 haloalkyl;

L 3 is selected from the group consisting of a bond, —C(O)N(R a3 )(C 1-6 alkylene)-, and —C(O)N(R a3 )(C 1-6 alkyleneoxy)-; and

R 3 is selected from the group consisting of C 1-6 haloalkyl, C 3-10 cycloalkyl, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl, wherein each C 1-6 haloalkyl, C 3-10 cycloalkyl, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl is optionally substituted by 1, 2, 3, or 4 substituents independently selected from OH, halo, and C 1-6 haloalkyl.

10. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein:

L 1 is selected from the group consisting of a bond and —C(O)(C 1-6 alkylene)-;

R 1 is selected from the group consisting of H and 4-10 membered heterocycloalkyl, wherein the 4-10 membered heterocycloalkyl is optionally substituted by 1, 2, 3, or 4 substituents independently selected from OH, halo, and C 1-6 haloalkyl;

L 2 is selected from the group consisting of —(C 1-6 alkylene)-(5-10 membered heteroarylene)-, —C(O)—, and —C(O)(C 1-6 alkylene)-;

R 2 is selected from the group consisting of C 1-6 alkoxy, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl, wherein each C 1-6 alkoxy, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl is optionally substituted by 1, 2, 3, or 4 substituents independently selected from OH, halo, and C 1-6 haloalkyl;

L 3 is selected from the group consisting of a bond, —C(O)N(R a3 )(C 1-6 alkylene)-, and —C(O)N(R a3 )(C 1-6 alkyleneoxy)-; and

R 3 is selected from the group consisting of C 1-6 haloalkyl, and 5-10 membered heteroaryl, wherein each C 1-6 haloalkyl, and 5-10 membered heteroaryl is optionally substituted by 1, 2, 3, or 4 substituents independently selected from OH, halo, and C 1-6 haloalkyl.

11. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein:

L 1 is selected from the group consisting of a bond and —C(O)(C 1-6 alkylene)-;

R 1 is selected from the group consisting of H and 4-10 membered heterocycloalkyl, wherein the 4-10 membered heterocycloalkyl is optionally substituted by one substituent independently selected from OH, halo, and C 1-6 haloalkyl;

L 2 is selected from the group consisting of —(C 1-6 alkylene)-(5-10 membered heteroarylene)-, —C(O)—, and —C(O)(C 1-6 alkylene)-;

R 2 is selected from the group consisting of C 1-6 alkoxy, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl, wherein each C 1-6 alkoxy, C 6-10 aryl, 4-10 membered heterocycloalkyl, and 5-10 membered heteroaryl is optionally substituted by one substituent independently selected from OH, halo, and C 1-6 haloalkyl;

L 3 is selected from the group consisting of a bond, —C(O)N(R a3 )(C 1-6 alkylene)-, and —C(O)N(R a3 )(C 1-6 alkyleneoxy)-; and

R 3 is selected from the group consisting of C 1-6 haloalkyl and 5-10 membered heteroaryl, wherein each C 1-6 haloalkyl and 5-10 membered heteroaryl is optionally substituted by one substituent independently selected from OH, halo, and C 1-6 haloalkyl.

12. The compound of claim 1 , wherein the compound is selected from the group consisting of:

or a pharmaceutically acceptable salt thereof.

13. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable carrier.

14. The compound of claim 1 , which is selected from:

or a pharmaceutically acceptable salt thereof.

15. A compound, which is:

or a pharmaceutically acceptable salt thereof.

16. A compound, which is selected from:

or a pharmaceutically acceptable salt thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 9, 2021
From: WANG, CUIHUA; CHEN, JOHN W.; KELIHER, EDMUND J.
To: THE GENERAL HOSPITAL CORPORATION
Reel/Frame 056798/0233 →
Continuity (2)
Provisional Application 62422912 · Nov 16, 2016
Related Publication 20190315689A1 · Oct 17, 2019