IP Library Granted Patent US 10,246,464
Granted Patent B2
US 10,246,464 · App. 15/509,989 · Granted Apr 2, 2019

Thienopyrimidine and thienopyridine compounds and methods of use thereof

Inventors: Jolanta Grembecka (Ann Arbor, MI); Tomasz Cierpicki (Ann Arbor, MI); Dmitry Borkin (Ann Arbor, MI); Jonathan Pollock (Ann Arbor, MI); Hongzhi Miao (Ann Arbor, MI); Duxin Sun (Ann Arbor, MI); Liansheng Li (La Jolla, CA); Tao Wu (La Jolla, CA); Jun Feng (La Jolla, CA); Pingda Ren (La Jolla, CA); Yi Liu (La Jolla, CA)
Assignees: THE REGENTS OF THE UNIVERSITY OF MICHIGAN; KURA ONCOLOGY, INC.
C07D495/04C07D519/00C07F9/5325C07F9/65583
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Quick Facts
Patent No.
US 10,246,464
App. No.
15/509,989
Granted
Apr 2, 2019
Kind
B2
Abstract

The present disclosure provides compounds and methods for inhibiting the interaction of menin with its upstream or downstream signaling molecules including but not limited to MLL1, MLL2 and MLL-fusion oncoproteins. Compounds of the disclosure may be used in methods for the treatment of a wide variety of cancers and other diseases associated with one or more of MLL1, MLL2, MLL fusion proteins, and menin.

Claims (36)

1. A compound represented by the structure of Formula (4):

or a salt thereof, wherein:

R 1 , R 2 , R 4 , R 5 , R 8 , and R a are independently selected from hydrogen, halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , —N(R 20 )S(O) 2 R 20 , —NO 2 , —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 1-6 alkyl, C 2-6 alkenyl, and C 2-6 alkynyl, each of which is independently optionally substituted at each occurrence with one or more substituents selected from halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , —N(R 20 )S(O) 2 R 20 , —NO 2 , ═O, ═S, ═N(R 20 ), —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 3-10 carbocycle, and 3- to 10-membered heterocycle, or two substituents on the same carbon atom of an C 1-6 alkyl, C 2-6 alkenyl, or C 2-6 alkynyl come together to form a C 3-10 carbocycle or 3- to 10-membered heterocycle; and C 3-10 carbocycle and 3- to 10-membered heterocycle; wherein any C 3 -10 carbocycle and 3- to 10-membered heterocycle of R 1 , R 2 , R 4 , R 5 , R 8 , and R a is independently optionally substituted with one or more substituents selected from halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , —N(R 20 )S(O) 2 R 20 , —NO 2 , ═O, ═S, ═N(R 20 ), —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 1-6 alkyl, C 2-6 alkenyl, and C 2-6 alkynyl;

R 3 is selected from selected from hydrogen, —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , C 1-6 alkyl, C 2-6 alkenyl, and C 2-6 alkynyl, each of which is independently optionally substituted at each occurrence with one or more substituents selected from halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , —N(R 20 )S(O) 2 R 20 , —NO2, ═O, ═S, ═N(R 20 ), —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 3-10 carbocycle, and 3- to 10-membered heterocycle, or two substituents on the same carbon atom of an C 1-6 alkyl, C 2-6 alkenyl, or C 2-6 alkynyl come together to form a C 3-10 carbocycle or 3- to 10-membered heterocycle; and C 3-10 carbocycle and 3- to 10-membered heterocycle; wherein any C 3-10 carbocycle and 3- to 10-membered heterocycle of R 3 is independently optionally substituted with one or more substituents selected from halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , —N(R 20 )S(O) 2 R 20 , —NO 2 , ═O, ═S, ═N(R 20 ), —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 1-6 alkyl, C 2-6 alkenyl, and C 2-6 alkynyl;

R 6 is independently selected at each occurrence from halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , —N(R 20 )S(O) 2 R 20 , —NO 2 , —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 1-6 alkyl, C 2-6 alkenyl, and C 2-6 alkynyl, each of which is independently optionally substituted at each occurrence with one or more substituents selected from halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , —N(R 20 )S(O) 2 R 20 , —NO 2 , ═O, ═S, ═N(R 20 ), —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 3-10 carbocycle, and 3- to 10-membered heterocycle, or two substituents on the same carbon atom of an C 1-6 alkyl, C 2-6 alkenyl, or C 2-6 alkynyl come together to form a C 3-10 carbocycle or 3- to 10-membered heterocycle; and C 3 -10o carbocycle and 3- to 10-membered heterocycle; wherein any C 3-10 carbocycle and 3- to 10-membered heterocycle of R 6 is independently optionally substituted with one or more substituents selected from halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 22 , —N(R 20 )S(O) 2 R 20 , —NO 2 , ═O, ═S, ═N(R 20 ), —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 1-6 alkyl, C 2-6 alkenyl, and C 2-6 alkynyl;

R 20 at each occurrence is independently selected from hydrogen; C 1-6 alkyl, C 2-6 alkenyl, and C 2-6 alkynyl, each of which is independently optionally substituted at each occurrence with one or more substituents selected from halogen, —OR 30 , —SR 30 , —N(R 30 ) 2 , —N(R 30 )C(O)R 30 , —C(O)R 30 , —C(O)OR 30 , —C(O)N(R 30 ) 2 , —OC(O)R 30 , —S(O) 2 R 30 , —S(O) 2 N(R 30 ) 2 , —N(R 30 )S(O) 2 R 30 , —NO 2 , —P(O)(OR 30 ) 2 , —P(O)(R 30 ) 2 , —OP(O)(OR 30 ) 2 , and —CN; and 3- to 10-membered heterocycle and C 3-10 carbocycle;

R 30 at each occurrence is independently selected from hydrogen, C 1-6 alkyl, C 2-6 alkenyl, and C 2-6 alkynyl;

Y is N or C(R a );

L is absent or selected from alkylene and heteroalkylene;

s is selected from 0, 1, 2, 3, and 4;

R 7a is -G-V-R 9a :

G is selected from alkylene, heteroalkylene, C 3-12 carbocycle, 3- to 12-membered heterocycle, and combinations thereof, wherein G is optionally substituted with one or more R 32 groups;

V is selected from a C 3-12 carbocycle, and 3- to 12-membered heterocycle;

wherein V is optionally substituted with one or more R 32 groups;

R 9a is selected from halogen, —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)OR 20 , —OC(O)R 20 , —N(R 20 )S(O) 2 R 20 , —NO 2 , =S, =N(R 20 ), —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 2-6 alkenyl, and C 2-6 alkynyl, each of which is independently optionally substituted at each occurrence with one or more substituents selected from halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , —N(R 20 )S(O) 2 R 20 , —NO 2 , ═O, ═S, ═N(R 20 ), —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 3-10 carbocycle, and 3- to 10-membered heterocycle; C 3-10 carbocycle and 3- to 10-membered heterocycle; or two R 32 on the same carbon atom can come together to form a C 3-10 carbocycle or 3- to 10-membered heterocycle, wherein each C 3-10 carbocycle and 3- to 10-membered heterocycle of R 32 is independently optionally substituted with one or more substituents selected from halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , —N(R 20 )S(O) 2 R 20 , —NO 2 , ═O, ═S, ═N(R 20 ), —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 1-6 alkyl, C 2-6 alkenyl, and C 2-6 alkynyl; and

R 32 at each occurrence is selected from halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , —N(R 20 )S(O) 2 R 20 , —NO 2 , ═O, ═S, ═N(R 20 ), —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 1-6 alkyl, C 2-6 alkenyl, and C 2-6 alkynyl, each of which is independently optionally substituted at each occurrence with one or more substituents selected from halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , —N(R 20 )S(O) 2 R 20 , —NO 2 , ═O, ═S, ═N(R 20 ), —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 3-10 carbocycle, and 3- to 10-membered heterocycle; C 3-10 carbocycle and 3- to 10-membered heterocycle; or two R 32 on the same carbon atom can come together to form a C 3-10 carbocycle or 3- to 10-membered heterocycle, wherein each C 3-10 carbocycle and 3- to 10-membered heterocycle of R 32 is independently optionally substituted with one or more substituents selected from halogen, —OR 20 , —SR 20 , —N(R 20 ) 2 , —N(R 20 )C(O)R 20 , —C(O)R 20 , —C(O)OR 20 , —C(O)N(R 20 ) 2 , —OC(O)R 20 , —S(O) 2 R 20 , —S(O) 2 N(R 20 ) 2 , —N(R 20 )S(O) 2 R 20 , —NO 2 , ═O, ═S, ═N(R 20 ), —P(O)(OR 20 ) 2 , —P(O)(R 20 ) 2 , —OP(O)(OR 20 ) 2 , —CN, C 1-6 alkyl, C 2-6 alkenyl, and C 2-6 alkynyl.

2. The compound or salt of claim 1 , wherein R 1 and R 2 are independently selected from hydrogen, halogen, —OH, —CN, —NO 2 , —NH 2 , C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 haloalkenyl, C 2-6 alkynyl, and C 2-6 haloalkynyl.

3. The compound or salt of claim 2 , wherein R 1 is selected from halogen, C 1-6 haloalkyl, C 2-6 haloalkenyl, and C 2-6 haloalkynyl.

4. The compound or salt of claim 3 , wherein R 1 is selected from —CH 2 CF 3 and —CH 2 CHF 2 .

5. The compound or salt of claim 2 , wherein R 2 is selected from hydrogen, halogen, —OH, —CN, —NO 2 , —NH 2 , C 1-6 alkyl, and C 1-6 alkoxy.

6. The compound or salt of claim 5 , wherein R 2 is hydrogen.

7. The compound or salt of claim 1 , wherein R 3 , R 4 , and R 5 are each hydrogen.

8. The compound or salt of claim 1 , wherein R 6 , at each occurrence, is independently selected from halogen, —OH, C 1-6 alkyl, and C 1-6 alkoxy.

9. The compound or salt of claim 1 , wherein R 8 is selected from hydrogen, halogen, —OH, —CN, —NO 2 , —NH 2 , C 1-6 alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, C 2-6 alkenyl, C 2-6 haloalkenyl, C 2-6 alkynyl, and C 2-6 haloalkynyl.

10. The compound or salt of claim 9 , wherein R 8 is —CN.

11. The compound or salt of claim 1 , wherein Y is N.

12. The compound or salt of claim 1 , wherein L is absent.

13. The compound or salt of claim 1 , wherein G is alkylene optionally substituted with one or more R 32 groups.

14. The compound or salt of claim 13 , wherein G is selected from:

15. The compound or salt of claim 1 , wherein V is selected from azetidine, oxetane, piperidine, oxane, piperazine, pyrrolidine, tetrahydrofuran, thiolane, imidazolidine, morpholine, thiomorpholine, azepane, and homopiperazine, any one of which is optionally substituted with one or more R 32 groups.

16. The compound or salt of claim 1 , wherein V is selected from phenyl, pyridine, pyrazine, pyrimidine, pyridazine, naphthalene, anthracene, quinoline, isoquinoline, quinoxaline, acridine, quinazoline, cinnoline, phthalazine, furan, dihydrofuran, thiophene, dihydrothiophene, imidazole, imidazoline, oxazole, oxazoline, pyrrole, dihydropyrrole, thiazole, dihydrothiazole, pyrazole, dihydropyrazole, isoxazole, dihydroisoxazole, isothiazole, dihydroisothiazole, benzofuran, isobenzofuran, indole, isoindole, benzothiophene, benzimidazole, purine, indazole, benzoxazole, benzisoxazole, and benzothiazole, any one of which is optionally substituted with one or more R 32 groups.

17. The compound or salt of claim 1 , wherein R 9a is

18. A compound selected from:

or a salt thereof.

19. A pharmaceutical composition, comprising a compound of claim 1 , or a salt thereof, and a pharmaceutically acceptable carrier or excipient.

20. A method for the treatment of a disease, comprising administering a compound of claim 1 , or a salt thereof, to a subject suffering from said disease, wherein said disease is leukemia, hematologic malignancies, solid tumor cancer, glioma, or diabetes.

Assignments (9)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2024
From: LIU, YI
To: WELLSPRING BIOSCIENCES LLC
Reel/Frame 069189/0086 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2024
From: LI, LIANSHENG
To: WELLSPRING BIOSCIENCES LLC
Reel/Frame 069324/0755 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2024
From: REN, PINGDA
To: WELLSPRING BIOSCIENCES LLC
Reel/Frame 069324/0800 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2024
From: WU, TAO
To: WELLSPRING BIOSCIENCES LLC
Reel/Frame 069324/0820 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2024
From: WELLSPRING BIOSCIENCES, INC.
To: KURA ONCOLOGY, INC.
Reel/Frame 069325/0179 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2024
From: FENG, JUN
To: WELLSPRING BIOSCIENCES LLC
Reel/Frame 069325/0878 →
CORRECTIVE ASSIGNMENT TO CORRECT THE APPLICATION NUMBER 15/059,989 PREVIOUSLY RECORDED ON REEL 043267 FRAME 0369. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT OF ASSIGNORS INTEREST. Recorded Aug 16, 2017
From: GREMBECKA, JOLANTA; CIERPICKI, TOMASZ; BORKIN, DMITRY; POLLOCK, JONATHAN; MIAO, HONGZHI; SUN, DUXIN
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
Reel/Frame 044068/0719 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 11, 2017
From: GREMBECKA, JOLANTA; CIERPICKI, TOMASZ; BORKIN, DMITRY; POLLOCK, JONATHAN; MIAO, HONGZHI; SUN, DUXIN
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
Reel/Frame 043267/0369 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 10, 2017
From: LI, LIANSHENG; WU, TAO; FENG, JUN; REN, PINGDA; LIU, YI
To: KURA ONCOLOGY, INC.
Reel/Frame 043264/0015 →
Continuity (5)
Provisional Application 62214681 · Sep 4, 2015
Provisional Application 62171124 · Jun 4, 2015
Provisional Application 62095588 · Dec 22, 2014
Provisional Application 62048036 · Sep 9, 2014
Related Publication 20170247391A1 · Aug 31, 2017
Cited By (1)
US 12,528,822