IP Library Granted Patent US 9,388,192
Granted Patent B2
US 9,388,192 · App. 14/654,779 · Granted Jul 12, 2016

Benzimidazole derivatives as Kinase Inhibitors

Inventors: Wojciech Czardybon (Mikolów, PL); Krzysztof Brzózka (Kraków, PL); Michal Galezowski (Skierniewice, PL); Renata Windak (Kraków, PL); Mariusz Milik (Kraków, PL); Magdalena Zawadzka (Gdansk, PL); Pawel Guzik (Kraków, PL); Ewelina Wincza (Wroclaw, PL); Marta Prokop (Gdynia, PL); Katarzyna Wiklik (Kraków, PL); Aleksandra Sabiniarz (Brzeg, PL); Wieslaw Marek Cholody (Frederick, MD); Raymond Horvath (Montreal, CA); Tomasz Rzymski (Elblag, PL)
Assignee: Selvita S.A.
C07D487/08C07D235/06C07D235/14C07D235/24C07D235/30C07D401/04C07D401/12C07D401/14C07D403/04C07D403/12C07D403/14C07D405/12C07D413/04C07D413/12
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Quick Facts
Patent No.
US 9,388,192
App. No.
14/654,779
Granted
Jul 12, 2016
Kind
B2
Abstract

The present invention relates to derivatives of benzimidazoles of formula (I) as disclosed herein as well as pharmaceutical compositions comprising said derivatives. The derivates according to the present invention are serine/threonine and tyrosine kinase-inhibitors, particularly of PIM1-3- and DYRK1A-kinases and may particularly be used in the treatment of diseases linked to these kinases, such as e.g. leukemias, lymphomas, solid tumors and autoimmune disorders.

Claims (62)

1. A compound of formula (I):

wherein

X 1 is selected from the group consisting of nitro, cyano, methyl, trifluoromethyl, —C(═O)T 1 , —C(═O)OT 4 and —S(═O) 2 T 4 ;

Z and X 2 are each independently selected from the group consisting of F, Cl, Br, I, —C 1-3 alkyl and trifluoromethyl, with the proviso that Z and X 2 are not both —C 1-3 alkyl;

X 3 is isopropyl or ethyl;

X 4 is either absent or selected from —NR 4 — and —N(R 4 )(CH 2 )—;

R 4 is selected from H and —C 1-6 alkyl;

Y 1 is a 4- to 7-membered saturated carbocycle or heterocycle, with the proviso that the point of attachment on said heterocycle is carbon if X 4 is —NR 4 — or —N(R 4 )(CH 2 )—, wherein said 4- to 7-membered carbocycle or heterocycle is optionally substituted with one or more substituents independently selected from F, —OT 1 , —N(T 2 )(T 3 ), —C(═O)N(T 2 )(T 3 ), —C(═O)OT 1 , —ST 1 , —S(═O)T 1 , —S(═O) 2 N(T 2 )(T 3 ), oxo, and —C 1-3 alkyl, wherein said —C 1-3 alkyl is optionally substituted with one or more substituents independently selected from —OT 7 , —N(T 2 )(T 3 ), and a 6-membered saturated heterocycle;

T 1 , T 2 and T 3 are each independently selected from H and —C 1-6 alkyl optionally substituted with one or more substituents independently selected from F, —N(T 5 )(T 6 ), —OT 7 , —ST 7 , cyano, —C(═O)OT 7 , —C(═O)N(T 5 )(T 6 ), —OC(═O)N(T 5 )(T 6 ), —S(═O) 2 T 7 , —S(═O) 2 OT 8 and —S(═O) 2 N(T 5 )(T 6 );

T 4 is —C 1-6 alkyl optionally substituted with one or more substituents independently selected from F, —N(T 5 )(T 6 ), —OT 7 , —ST 7 , cyano, —C(═O)OT 7 , —C(═O)N(T 5 )(T 6 ), —OC(═O)N(T 5 )(T 6 ), —S(═O) 2 T 8 , —S(═O) 2 OT 7 and —S(═O) 2 N(T 5 )(T 6 );

T 5 , T 6 and T 7 are each independently selected from H and —C 1-6 alkyl optionally substituted with one or more substituents independently selected from F, amino, hydroxyl, thiol and cyano; and

T 8 is selected from —C 1-6 alkyl optionally substituted with one or more substituents independently selected from F, amino, hydroxyl, thiol and cyano;

or a pharmaceutically acceptable salt thereof.

2. A compound according to claim 1 , wherein X 1 is selected from the group consisting of nitro, cyano, trifluoromethyl, —C(═O)T 1 , and —S(═O) 2 T 4 ;

or a pharmaceutically acceptable salt thereof.

3. A compound according to claim 1 , wherein Z and X 2 are each independently selected from the group consisting of F, Cl, Br, I, and trifluoromethyl;

or a pharmaceutically acceptable salt thereof.

4. A compound according to claim 1 , wherein X 4 is absent;

or a pharmaceutically acceptable salt thereof.

5. A compound according to claim 1 , wherein X 4 is absent and Y 1 is a 6-membered saturated heterocycle wherein said 6-membered heterocycle is optionally substituted with one or more substituents independently selected from F, —OT 1 , —N(T 2 )(T 3 ), —C(═O)N(T 2 )(T 3 ), —C(═O)OT 1 , —ST 1 , —S(═O) 2 T 1 , —S(═O) 2 N(T 2 )(T 3 ), oxo and —C 1-3 alkyl;

or a pharmaceutically acceptable salt thereof.

6. A compound according to claim 1 , wherein said compound is selected from the group consisting of:

5,6-dibromo-1-ethyl-4-nitro-2-(piperazin-1-yl)-1H-1,3-benzodiazole;

5,6-dibromo-4-nitro-2-(piperazin-1-yl)-1-(propan-2-yl)-1H-1,3-benzodiazole;

(3S)-1-(5,6-dibromo-1-ethyl-4-nitro-1H-1,3-benzodiazol-2-yl)piperidin-3-amine;

5,6-dibromo-2-[(2S)-2-methylpiperazin-1-yl]-4-nitro-1-(propan-2-yl)-1H-1,3-benzodiazole; and

5,6-dibromo-4-nitro-2-(piperidin-4-yl)-1-(propan-2-yl)-1H-1,3-benzodiazole;

or a pharmaceutically acceptable salt thereof.

7. A compound according to claim 1 , wherein the pharmaceutically acceptable salt is selected from the group consisting of the hydrochloride, hydrobromide, hydroiodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate, isonicotinate, acetate, lactate, salicylate, citrate, tartrate, pantothenate, bitartrate, ascorbate, succinate, maleate, gentisinate, fumarate, gluconate, glucaronate, saccharate, formate, benzoate, glutamate, methanesulfonate, ethanesulfonate, benzensulfonate, p-toluenesulfonate and pamoate.

8. A pharmaceutical composition comprising a compound of claim 1

or a pharmaceutically acceptable salt thereof.

9. A method for treating a disease in a subject, comprising administering to a subject in need of said treating a pharmaceutical composition according to claim 8 , wherein said disease is selected from the group consisting of prostate cancer; a leukemia; and a lymphoma.

10. A compound of claim 1 , wherein:

X 1 is selected from the group consisting of nitro, cyano, trifluoromethyl, —C(═O)T 1 , and —S(═O) 2 T 4 , and

Z and X 2 are each independently selected from the group consisting of F, Cl, Br, I, and trifluoromethyl;

or a pharmaceutically acceptable salt thereof.

11. A compound of claim 10 , wherein X 4 is absent;

or a pharmaceutically acceptable salt thereof.

12. A pharmaceutical composition according to claim 8 , wherein said compound is selected from the group consisting of:

5,6-dibromo-1-ethyl-4-nitro-2-(piperazin-1-yl)-1H-1,3-benzodiazole;

5,6-dibromo-4-nitro-2-(piperazin-1-yl)-1-(propan-2-yl)-1H-1,3-benzodiazole;

(3S)-1-(5,6-dibromo-1-ethyl-4-nitro-1H-1,3-benzodiazol-2-yl)piperidin-3-amine;

5,6-dibromo-2-[(2S)-2-methylpiperazin-1-yl]-4-nitro-1-(propan-2-yl)-1H-1,3-benzodiazole; and

5,6-dibromo-4-nitro-2-(piperidin-4-yl)-1-(propan-2-yl)-1H-1,3-benzodiazole;

or a pharmaceutically acceptable salt thereof.

13. A method for treating a disease in a subject, comprising administering to a subject in need of said treating a pharmaceutical composition according to claim 12 , wherein said disease is selected from the group consisting of prostate cancer; a leukemia; and a lymphoma.

14. The method of claim 9 , wherein said disease is prostate cancer.

15. The method of claim 9 , wherein said disease is a leukemia selected from acute lymphoblastic leukemia, acute myeloid leukemia, and chronic lymphocytic leukemia.

16. The method of claim 9 , wherein said disease is a lymphoma selected from diffuse large B-cell lymphoma.

17. The compound according to claim 6 , wherein said compound is selected from the group consisting of:

the hydrochloride salt of 5,6-dibromo-1-ethyl-4-nitro-2-(piperazin-1-yl)-1H-1,3-benzodiazole;

the hydrochloride salt of 5,6-dibromo-4-nitro-2-(piperazin-1-yl)-1-(propan-2-yl)-1H-1,3-benzodiazole;

the hydrochloride salt of (3S)-1-(5,6-dibromo-1-ethyl-4-nitro-1H-1,3-benzodiazol-2-yl)piperidin-3-amine;

the hydrochloride salt of 5,6-dibromo-2-[(2S)-2-methylpiperazin-1-yl]-4-nitro-1-(propan-2-yl)-1H-1,3-benzodiazole; and

the hydrochloride salt of 5,6-dibromo-4-nitro-2-(piperidin-4-yl)-1-(propan-2-yl)-1H-1,3-benzodiazole.

18. A pharmaceutical composition according to claim 12 , wherein said compound is selected from the group consisting of:

the hydrochloride salt of 5,6-dibromo-1-ethyl-4-nitro-2-(piperazin-1-yl)-1H-1,3-benzodiazole;

the hydrochloride salt of 5,6-dibromo-4-nitro-2-(piperazin-1-yl)-1-(propan-2-yl)-1H-1,3-benzodiazole;

the hydrochloride salt of (3 S)-1-(5,6-dibromo-1-ethyl-4-nitro-1H-1,3-benzodiazol-2-yl)piperidin-3-amine;

the hydrochloride salt of 5,6-dibromo-2-[(2S)-2-methylpiperazin-1-yl]-4-nitro-1-(propan-2-yl)-1H-1,3-benzodiazole; and

the hydrochloride salt of 5,6-dibromo-4-nitro-2-(piperidin-4-yl)-1-(propan-2-yl)-1H-1,3-benzodiazole.

19. A method for treating a disease in a subject, comprising administering to a subject in need of said treating a pharmaceutical composition according to claim 18 , wherein said disease is selected from the group consisting of prostate cancer; a leukemia; and a lymphoma.

Assignments (3)
CHANGE OF NAME Recorded Feb 14, 2020
From: SELVITA S.A.
To: RYVU THERAPEUTICS S.A.
Reel/Frame 051944/0026 →
LICENSE Recorded Oct 24, 2017
From: SELVITA S.A.
To: BERLIN-CHEMIE AG
Reel/Frame 043936/0704 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 20, 2015
From: CZARDYBON, WOJCIECH; BRZÓZKA, KRZYSZTOF; GALEZOWSKI, MICHAL; WINDAK, RENATA; MILIK, MARIUSZ; ZAWADZKA, MAGDALENA; GUZIK, PAWEL; WINCZA, EWELINA; PROKOP, MARTA; WIKLIK, KATARZYNA; SABINIARZ, ALEKSANDRA; CHOLODY, WIESLAW MAREK; HORVATH, RAYMOND; RZYMSKI, TOMASZ
To: SELVITA SA
Reel/Frame 036382/0291 →
Priority Claims (1)
GB 1223265.8 · Dec 21, 2012 · national
Continuity (1)
Related Publication 20150336967A1 · Nov 26, 2015