IP Library Granted Patent US 10,464,911
Granted Patent B2
US 10,464,911 · App. 15/747,850 · Granted Nov 5, 2019

1,3,4-oxadiazole sulfamide derivative compounds as histone deacetylase 6 inhibitor, and the pharmaceutical composition comprising the same

Inventors: Jaekwang Lee (Gyeonggi-do, KR); Younghue Han (Gyeonggi-do, KR); Yuntae Kim (Gyeonggi-do, KR); Jaeki Min (Gyeonggi-do, KR); Miseon Bae (Gyeonggi-do, KR); Dohoon Kim (Gyeonggi-do, KR); Seokmin Jin (Gyeonggi-do, KR); Jangbeen Kyung (Gyeonggi-do, KR)
Assignee: Chong Kun Dang Pharmaceutical Corp.
C07D271/10A61P3/00A61P5/00A61P9/00A61P11/00A61P17/00A61P25/00A61P31/00A61P35/00C07D413/04C07D413/12C07D413/14C07D471/10
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Quick Facts
Patent No.
US 10,464,911
App. No.
15/747,850
Granted
Nov 5, 2019
Kind
B2
Abstract

The present invention relates to novel compounds having histone deacetylase 6 (HDAC6) inhibitory activity, stereoisomers thereof or pharmaceutically acceptable salts thereof, the use thereof for the preparation of therapeutic medicaments, pharmaceutical compositions containing the same, a method for treating diseases using the composition, and methods for preparing the novel compounds. The novel compounds, stereoisomers thereof or pharmaceutically acceptable salts thereof according to the present invention have histone deacetylase (HDAC) inhibitory activity and are effective for the prevention or treatment of HDAC6-mediated diseases, including infectious diseases; neoplasms; endocrine, nutritional and metabolic diseases; mental and behavioral disorders; neurological diseases; diseases of the eye and adnexa; cardiovascular diseases; respiratory diseases; digestive diseases; diseases of the skin and subcutaneous tissue; diseases of the musculoskeletal system and connective tissue; or congenital malformations, deformations and chromosomal abnormalities.

Claims (350)

1. A 1,3,4-oxadiazole sulfamide compound represented by the following formula I:

wherein L 1 , L 2 and L 3 are each independently a bond or -(C 1 -C 2 alkylene)-;

Z 1 to Z 4 are each independently N or CR Z , wherein R Z is —H or —X;

R 1 is —CX 2 H or —CX 3 ;

R 2 is

wherein Y is —N—, —O— or —S(═O) 2 —,

a to d are each independently an integer of 1, 2 or 3,

Ra to Rd are each independently —H or -(C 1 -C 4 alkyl),

the dotted line is a single bond or a double bond,

R 4 and R 5 are each independently -H, -X, -(C 1 -C 4 alkyl), -aryl or —NReRf, provided that when the dotted line is a double bond, R 5 is null,

Re and Rf are each independently —H or -(C 1 -C 4 alkyl),

when Y is —N—, R 6 and R 7 are each independently -H, -(C 1 -C 4 alkyl), -(C 1 -C 4 alkyl)-O—(C 1 -C 4 alkyl), —C(═O)-(C 1 -C 4 alkyl), —C(═O)—O(C 1 -C 4 alkyl), —C(═O)—CF 3 , -(C 1 -C 4 alkyl)-C(═O)—O(C 1 -C 4 alkyl), —S(═O) 2 -(C 1 -C 4 alkyl), -(C 3 -C 7 cycloalkyl), -(C 2 -C 6 heterocycloalkyl), -aryl, -(C 1 -C 4 alkyl)-aryl, -heteroaryl or amine protecting group, wherein at least one H of the -(C 1 -C 4 alkyl) may be substituted with —X or —OH, at least one H of the -aryl, —(C 1 -C 4 alkyl)-aryl or -heteroaryl may be substituted with —X, —OH or —CF 3 , and the -(C 2 -C 6 heterocycloalkyl) may contain an N, O or S atom in the ring,

and when Y is —O— or —S(═O) 2 —, R 6 and R 7 are null,

R 8 and R 9 are each independently -H, -(C 1 -C 4 alkyl), -(C 3 -C 7 cycloalkyl), -(C 2 -C 6 heterocycloalkyl), -(C 1 -C 4 alkyl)-(C 2 -C 6 heterocycloalkyl), -aryl, -heteroaryl or -(C 1 -C 4 alkyl)-aryl, wherein at least one H of the -(C 3 -C 7 cycloalkyl), -(C 2 -C 6 heterocycloalkyl), -(C 1 -C 4 alkyl)-(C 2 -C 6 heterocycloalkyl), -aryl, -heteroaryl or -(C 1 -C 4 alkyl) -aryl may be substituted with -(C 1 -C 4 alkyl), —C(═O)-(C 1 -C 4 alkyl), —S(═O) 2 -(C 1 -C 4 alkyl) or -(C 2 -C 6 heterocycloalkyl); and

R 3 is —H, -(C 1 -C 4 alkyl), -(C 1 -C 4 alkyl) -O(C 1 -C 4 alkyl), -(C 1 -C 4 alkyl) -C(═O)—O(C 1 -C 4 alkyl), -(C 3 -C 7 cycloalkyl), -aryl, -heteroaryl or

wherein at least one H of the -(C 3 -C 7 cycloalkyl), -aryl or -heteroaryl may be substituted with —X, —OH, -(C 1 -C 4 alkyl), —CF 3 , -(C 1 -C 4 alkyl)-(C 2 -C 6 heterocycloalkyl)-(C 1 -C 4 alkyl), —C(═O)-(C 1 -C 4 alkyl), —C(═O)—O(C 1 -C 4 alkyl), -O(C 1 -C 4 alkyl), -OCF 3 , —S(═O) 2 -(C 1 -C 4 alkyl), -aryl, -heteroaryl or —NR 11 R 12 ,

R 11 and R 12 are each independently —H or -(C 1 -C 4 alkyl),

R 1 , L 1 , Z 1 , Z 2 , Z 3 and Z 4 are as defined above; and

X is F, Cl, Br or I; and stereoisomers and pharmaceutically acceptable salts thereof.

2. The 1,3,4-oxadiazole sulfamide compound according to claim 1 ,

wherein L 1 and L 3 are each independently a bond;

L 2 is -(C 1 alkylene)-;

Z 1 to Z 4 are each independently N or CR Z , wherein R Z is —H or —X;

R 1 is —CX 2 H or —CX 3 ;

R 2 is

wherein Y is —N—, —O— or —S(═O) 2 -,

a to d are each independently an integer of 1 or 2,

Ra to Rd are each independently —H or -(C 1 -C 4 alkyl),

when Y is —N—, R 6 and R 7 are each independently -H, -(C 1 -C 4 alkyl), —C(═O)-(C 1 -C 4 alkyl), —S(═O) 2 -(C 1 -C 4 alkyl), -(C 3 -C 7 cycloalkyl) or -(C 2 -C 6 heterocycloalkyl), wherein at least one H of -(C 1 -C 4 alkyl) may be substituted with —X or —OH, and -(C 2 -C 6 heterocycloalkyl) may contain an N, O or S atom in the ring,

and when Y is —O— or —S(═O) 2 —, R 6 and R 7 are null,

R 8 and R 9 are each independently -H, -(C 1 -C 4 alkyl) or -(C 1 -C 4 alkyl)-(C 2 -C 6 heterocycloalkyl), wherein at least one H of the —(C 1 -C 4 alkyl)-(C 2 -C 6 heterocycloalkyl) may be substituted with —(C 1 -C 4 alkyl), —C(═O)-(C 1 -C 4 alkyl), —S(═O) 2 -(C 1 -C 4 alkyl) or -(C 2 -C 6 heterocycloalkyl);

R 3 is -aryl or -heteroaryl, wherein at least one H of the -aryl or -heteroaryl may be substituted with —X; and

X is F, Cl, Br or I.

3. The 1,3,4-oxadiazole sulfamide compound according to claim 2 ,

wherein L 1 or L 3 are each independently a bond;

L 2 is -(C 1 alkylene)-;

Z 1 to Z 4 are each independently N or CR Z , wherein R Z is —H or —X;

R 1 is —CF 2 H or —CF 3 ;

R 2 is

wherein Y is —N— or —S(═O) 2 -,

a to d are each independently an integer of 1 or 2,

Ra to Rd are each independently —H or -(C 1 -C 4 alkyl),

when Y is —N—, R 6 and R 7 are each independently -H, -(C 1 -C 4 alkyl), —C(═O)-(C 1 -C 4 alkyl), —S(═O) 2 -(C 1 -C 4 alkyl), -(C 3 -C 7 cycloalkyl) or -(C 2 -C 6 heterocycloalkyl), wherein at least one H of the -(C 1 -C 4 alkyl) may be substituted with —X or —OH, and the —(C 2 -C 6 heterocycloalkyl) may contain an N, O or S atom in the ring,

and when Y is —S(═O) 2 —, R 6 and R 7 are null;

R 3 is -aryl or -heteroaryl, wherein at least one H of the -aryl or -heteroaryl may be substituted with —X; and

X is F, Cl, Br or I.

4. The 1,3,4-oxadiazole sulfamide compound according to claim 3 ,

wherein L 1 or L 3 are each independently a bond;

L 2 is -(C 1 alkylene)-;

Z 1 to Z 4 are each independently N or CR Z , wherein R Z is —H or —X;

R 1 is —CF 2 H or —CF 3 ;

R 2 is

wherein Y is —N— or —S(═O) 2 -,

a and b are 2, c and d are 1,

Ra to Rd are each independently —H or -(C 1 -C 4 alkyl),

when Y is —N—, R 6 and R 7 are each independently -H, -(C 1 -C 4 alkyl), —C(═O)-(C 1 -C 4 alkyl), —S(═O) 2 -(C 1 -C 4 alkyl), -(C 3 -C 7 cycloalkyl) or -(C 2 -C 6 heterocycloalkyl), wherein at least one H of the -(C 1 -C 4 alkyl) may be substituted with —X or —OH, and the —(C 2 -C 6 heterocycloalkyl) may contain an N, O or S atom in the ring,

and when Y is —S(═O) 2 —, R 6 and R 7 are null;

R 3 is -aryl or -heteroaryl, wherein at least one H of the -aryl or -heteroaryl may be substituted with —F; and

X is F or Cl.

5. A 1,3,4-oxadiazole sulfamide compound selected from the group consisting of the compounds set forth below, and stereoisomers and pharmaceutically acceptable salts thereof:

Ex.

Comp.

Structure

 1

11198

 2

11199

 3

11293

 4

11294

 5

11295

 6

11296

 7

11297

 8

11298

 9

11299

10

11300

11

11301

12

11302

13

11303

14

11304

15

11305

16

11306

17

11307

18

11308

19

11309

20

11310

21

11311

22

11312

23

11313

24

11314

25

11315

26

11316

27

11317

28

11318

29

11319

30

11320

31

11321

32

11322

33

11363

34

11379

35

11440

36

11498

37

11527

38

11528

39

11574

40

11575

41

11640

42

11641

43

11642

44

11643

45

11644

46

11651

47

11652

48

11653

49

11654

50

11659

51

11660

52

11661

53

11662

54

11670

55

11671

56

11672

57

11673

58

11674

59

11702

60

11704

61

11713

62

11714

63

11787

64

11788

65

11789

66

11823

67

11824

68

11825

69

11826

70

11827

71

11828

72

11829

73

11830

74

11831

75

11832

76

11833

6. A 1,3,4-oxadiazole sulfamide compound according to claim 5 , selected from the group consisting of the compounds set forth below:

Ex.

Comp.

Structure

11

11301

12

11302

13

11303

15

11305

16

11306

17

11307

18

11308

23

11313

24

11314

25

11315

26

11316

28

11318

31

11321

33

11363

34

11379

35

11440

36

11498

39

11574

40

11575

42

11641

48

11653

49

11654

50

11659

53

11662

54

11670

55

11671

56

11672

66

11823

67

11824

68

11825

69

11826

70

11827

71

11828

72

11829

73

11830

74

11831

75

11832

76

11833

7. A 1,3,4-oxadiazole sulfamide compound according to claim 6 , selected from the group consisting of the compounds set forth below:

Ex.

Comp.

Structure

11

11301

12

11302

13

11303

15

11305

16

11306

23

11313

24

11314

25

11315

26

11316

33

11363

34

11379

35

11440

36

11498

39

11574

42

11641

49

11654

50

11659

54

11670

55

11671

56

11672

68

11825

72

11829

73

11830

74

11831

75

11832

8. A pharmaceutical composition comprising, as an active ingredient, a compound according to claim 1 and stereoisomers and pharmaceutically acceptable salts thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 23, 2018
From: LEE, JAEKWANG; HAN, YOUNGHUE; KIM, YUNTAE; MIN, JAEKI; BAE, MISEON; KIM, DOHOON; JIN, SEOKMIN; KYUNG, JANGBEEN
To: CHONG KUN DANG PHARMACEUTICAL CORP.
Reel/Frame 045016/0637 →
Priority Claims (1)
KR 10-2015-0106177 · Jul 27, 2015 · national
Continuity (1)
Related Publication 20180230113A1 · Aug 16, 2018
Cited By (3)
US 12,201,617 US 12,312,345 US 12,440,484