Substituted purine compounds

Patent metadata

Field	Value
Publication number	US-10400005-B2
Application number	US-201715632173-A
Country	US
Kind code	B2
Filing date	Jun 23, 2017
Priority date	Jul 3, 2013
Publication date	Sep 3, 2019
Grant date	Sep 3, 2019

Abstract

The present invention relates to substituted purine compounds. The present invention also relates to pharmaceutical compositions containing these compounds and methods of treating disorders in which DOT1-mediated protein methylation plays a part, such as cancer, by administering these compounds and pharmaceutical compositions to subjects in need thereof.

First claim

What is claimed is:

1. A compound of Formula (II):

or a pharmaceutically acceptable salt or ester thereof, wherein
R 1 is t-butyl substituted with one or more substituents selected from hydroxyl and oxo;
R 2 is H, hydroxyl, unsubstituted i-propyl, or i-propyl substituted with one or more hydroxyl;
l′ is 0, 1, 2, or 3;
each of m′ and n′, independently, is 0, 1, or 2;
each of p′, q′, r′, t′, u′, v′, and w′, independently, is 0 or 1; and
when R 1 is t-butyl substituted with only one hydroxyl, R 2 is H, hydroxyl, or i-propyl substituted with one or more hydroxyl; and wherein
(1) the compound of Formula (II) is a carboxylic acid;
(2) R 1 is t-butyl substituted with one hydroxyl, and (i) R 2 is H, and each of l′, m′, n′, u′, v′, and w′ is 0, (ii) R 2 is hydroxyl or i-propyl substituted with one or two hydroxyl, and each of l′, m′, n′, u′, v′, and w′ is 0, or (iii) R 2 is H, hydroxyl or i-propyl optionally substituted with one hydroxyl, and the sum of l′, m′, n′, u′, v′, and w′ is 1;
(3) R 1 is t-butyl substituted with two hydroxyl, and (i) R 2 is H, hydroxyl or i-propyl optionally substituted with one hydroxyl, and each of l′, m′, n′, u′, v′, and w′ is 0, or (ii) R 2 is H, hydroxyl or i-propyl optionally substituted with one hydroxyl, and the sum of l′, m′, n′, u′, v′, and w′ is 1, or
(4) R 1 is t-butyl substituted with three hydroxyl, R 2 is H or unsubstituted i-propyl, and each of l′, m′, n′, u′, v′, and w′ is 0.

2. The compound of claim 1 or the pharmaceutically acceptable salt or ester thereof, being in an isolated form.

3. The compound of claim 1 , being of Formula (IIA):

or Formula (IIB):

4. The compound of claim 1 , comprising one hydroxyl in addition to the two hydroxyls on the tetrahydrofuran ring.

5. The compound of claim 1 , wherein R 1 is t-butyl substituted with one hydroxyl, R 2 is H, and each of l′, m′, n′, u′, v′, and w′ is 0.

6. The compound of claim 1 , being of a carboxylic acid.

7. The compound of claim 1 , wherein R 1 is t-butyl substituted with one hydroxyl and one oxo, and wherein the hydroxyl and oxo together with the carbon to which they are attached form —COOH.

8. The compound of claim 1 , wherein R 1 is —C(CH 3 ) 2 COOH), R 2 is H or unsubstituted i-propyl, and each of l′, m′, n′, u′, v′, and w′ is 0.

9. The compound of claim 1 , comprising two or three hydroxyls in addition to the two hydroxyls on the tetrahydrofuran ring.

10. The compound of claim 1 , wherein R 1 is t-butyl substituted with one hydroxyl, and (i) R 2 is hydroxyl or i-propyl substituted with one or two hydroxyl, and each of l′, m′, n′, u′, v′, and w′ is 0, or (ii) R 2 is H, hydroxyl, or i-propyl optionally substituted with one hydroxyl, and the sum of l′, m′, n′, u′, v′, and w′ is 1.

11. The compound of claim 1 , wherein R 1 is t-butyl substituted with two hydroxyl, and (i) R 2 is H, hydroxyl or i-propyl optionally substituted with one hydroxyl, and each of l′, m′, n′, u′, v′, and w′ is 0, or (ii) R 2 is H, hydroxyl or i-propyl optionally substituted with one hydroxyl, and the sum of l′, m′, n′, u′, v′, and w′ is 1.

12. The compound of claim 1 , wherein R 1 is t-butyl substituted with three hydroxyl, R 2 is H or unsubstituted i-propyl, and each of l′, m′, n′, u′, v′, and w′ is 0.

13. The compound of claim 1 , comprising four hydroxyls in addition to the two hydroxyls on the tetrahydrofuran ring.

14. The compound of claim 1 , comprising five or more hydroxyls in addition to the two hydroxyls on the tetrahydrofuran ring.

15. The compound of claim 1 , wherein the compound is selected from the group consisting of Compounds 49-54, 56, 57, 63-89, 107, and 110-112.

16. A pharmaceutical composition comprising a compound of Formula (II):

or a pharmaceutically acceptable salt or ester thereof, and a pharmaceutically acceptable carrier, wherein
R 1 is t-butyl substituted with one or more substituents selected from hydroxyl and oxo;
R 2 is H, hydroxyl, unsubstituted i-propyl, or i-propyl substituted with one or more hydroxyl;
l′ is 0, 1, 2, or 3;
each of m′ and n′, independently, is 0, 1, or 2;
each of p′, q′, r′, t′, u′, v′, and w′, independently, is 0 or 1; and
when R 1 is t-butyl substituted with only one hydroxyl, R 2 is H, hydroxyl, or i-propyl substituted with one or more hydroxyl; and wherein
(1) the compound of Formula (II) is a carboxylic acid;
(2) R 1 is t-butyl substituted with one hydroxyl, and (i) R 2 is H, and each of l′, m′, n′, u′, v′, and w′ is 0, (ii) R 2 is hydroxyl or i-propyl substituted with one or two hydroxyl, and each of l′, m′, n′, u′, v′, and w′ is 0, or (iii) R 2 is H, hydroxyl or i-propyl optionally substituted with one hydroxyl, and the sum of l′, m′, n′, u′, v′, and w′ is 1;
(3) R 1 is t-butyl substituted with two hydroxyl, and (i) R 2 is H, hydroxyl or i-propyl optionally substituted with one hydroxyl, and each of l′, m′, n′, u′, v′, and w′ is 0, or (ii) R 2 is H, hydroxyl or i-propyl optionally substituted with one hydroxyl, and the sum of l′, m′, n′, u′, v′, and w′ is 1; or
(4) R 1 is t-butyl substituted with three hydroxyl, R 2 is H or unsubstituted i-propyl, and each of l′, m′, n′, u′, v′, and w′ is 0.

17. The pharmaceutical composition of claim 16 , wherein the compound of Formula (II) or the pharmaceutically acceptable salt or ester thereof is in an isolated form.

18. A method of treating cancer comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition of claim 16 .

19. A method of treating hematological cancer comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition of claim 16 .

20. A method of treating a disorder mediated by a translocation of a gene on chromosome 11q23, comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition of claim 16 .

21. A method of treating a disorder mediated by DOT1L-mediated protein methylation, comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition of claim 16 .

22. A method of treating leukemia comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition of claim 16 .

23. The method of claim 22 , wherein the leukemia is acute myeloid leukemia, acute lymphocytic leukemia or mixed lineage leukemia.

24. The method of claim 22 , wherein the leukemia is characterized by a chromosomal rearrangement.

25. The method of claim 24 , wherein said chromosomal rearrangement is chimeric fusion of mixed lineage leukemia gene (MLL) or partial tandem duplication of MLL (MLL-PTD).

26. The method of claim 25 , wherein the subject has an increased level of HOXA9, Fms-like tyrosine kinase 3 (FLT3), MEIS1, and/or DOT1L.

27. A method for treating leukemia in a subject comprising:
1) (a) detecting the level of HOXA9, FLT3, MEIS1, and/or DOT1L in a

Assignees

• Epizyme Inc

Inventors

• Waters Nigel J

Classifications

• G01N33/57505

  of the blood, e.g. leukaemia · CPC title

• G01N33/5758

  involving compounds serving as markers for tumours, cancers or neoplasias, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides or metabolites · CPC title

• C12Q2600/158

  Expression markers · CPC title

• A61K31/706

  containing six-membered rings with nitrogen as a ring hetero atom · CPC title

• C12Q1/6886

  for cancer (immunoassay for cancer G01N33/575) · CPC title