IP Library Granted Patent US 10,253,046
Granted Patent B2
US 10,253,046 · App. 15/590,523 · Granted Apr 9, 2019

TYK2 inhibitors and uses thereof

Inventors: Markus Dahlgren (Stratford, CT); Jeremy Robert Greenwood (Brooklyn, NY); Geraldine C. Harriman (Charlestown, RI); Joshua Jahmil Kennedy-Smith (New York, NY); Craig E. Masse (Cambridge, MA); Donna L. Romero (Chesterfield, MO); Mee Shelley (Tigard, OR); Ronald T. Wester (Ledyard, CT)
Assignee: Nimbus Lakshmi
C07D519/00A61P35/00A61P37/00C07D471/04C07D487/04C07F5/025C07F5/027
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Quick Facts
Patent No.
US 10,253,046
App. No.
15/590,523
Granted
Apr 9, 2019
Kind
B2
Abstract

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of TYK2, and the treatment of TYK2-mediated disorders.

Claims (125)

1. A compound of formula I:

or a pharmaceutically acceptable salt thereof, wherein:

each of X and Y is independently ═C(R 6 )—, ═N—, or ═N + (→O − )—, provided that X and Y are not simultaneously ═C(R 6 )—;

Ring A is phenyl; a 5-6 membered heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, and sulfur; a 3-6 membered saturated or partially unsaturated heterocyclic ring having 1-2 heteroatoms independently selected from nitrogen, oxygen, and sulfur; or a 4-6 membered saturated or partially unsaturated carbocyclic ring; wherein Ring A is substituted with m instances of R 7 ;

each of R 1 and R 1′ is independently hydrogen, —R 2 , halogen, —CN, —NO 2 , —OR, —SR, —NR 2 , —S(O) 2 R, —S(O) 2 NR 2 , —S(O)R, —C(O)R, —C(O)OR, —C(O)NR 2 , —C(O)N(R)OR, —OC(O)R, —OC(O)NR 2 , —N(R)C(O)OR, —N(R)C(O)R, —N(R)C(O)NR 2 , or —N(R)S(O) 2 R; or

R 1 and R 1′ are taken together to form an oxo group or with their intervening atoms to form an optionally substituted 3-7 membered spiro-fused ring having 0-2 heteroatoms independently selected from nitrogen, oxygen, and sulfur;

each R 2 is independently an optionally substituted group selected from C 1-6 aliphatic, phenyl, a 4-7 membered saturated or partially unsaturated heterocyclic ring having 1-2 heteroatoms independently selected from nitrogen, oxygen, and sulfur, and a 5-6 membered heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, and sulfur;

R 3 is a group selected from C 1-6 alkyl, phenyl, a 3-7 membered saturated or partially unsaturated carbocyclic ring, a 3-7 membered saturated or partially unsaturated heterocyclic ring having 1-2 heteroatoms independently selected from nitrogen, oxygen, and sulfur, and a 5-6 membered heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein R 3 is substituted with n instances of R 8 ;

R 4 is hydrogen or optionally substituted C 1-6 aliphatic;

R 5′ is an 8-14 membered saturated or partially unsaturated heterocyclic ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, and sulfur; wherein R 5′ is substituted with p instances of R 9 ;

R 6 is hydrogen, —R 2 , halogen, —CN, —NO 2 , —OR, —SR, —NR 2 , —S(O) 2 R, —S(O) 2 NR 2 , —S(O)R, —C(O)R, —C(O)OR, —C(O)NR 2 , —C(O)N(R)OR, —OC(O)R, —OC(O)NR 2 , —N(R)C(O)OR, —N(R)C(O)R, —N(R)C(O)NR 2 , or —N(R)S(O) 2 R;

each instance of R 7 , R 8 , R 10 , and R 11 is independently oxo, —R 2 , halogen, —CN, —NO 2 , —OR, —SR, —NR 2 , —S(O) 2 R, —S(O) 2 NR 2 , —S(O)R, —C(O)R, —C(O)OR, —C(O)NR 2 , —C(O)N(R)OR, —OC(O)R, —OC(O)NR 2 , —N(R)C(O)OR, —N(R)C(O)R, —N(R)C(O)NR 2 , or —N(R)S(O) 2 R;

each instance of R 9 is independently oxo, C 1-6 hydroxyaliphatic, —R 2 , halogen, —CN, —NO 2 , —OR, —SR, —NR 2 , —S(O) 2 R, —S(O) 2 NR 2 , —S(O)R, —C(O)R, —C(O)OR, —C(O)NR 2 , —C(O)N(R)OR, —OC(O)R, —OC(O)NR 2 , —N(R)C(O)OR, —N(R)C(O)R, —N(R)C(O)NR 2 , or —N(R)S(O) 2 R;

L 1 is a covalent bond or a C 1-6 bivalent saturated or unsaturated, straight or branched hydrocarbon chain wherein one or two methylene units of the chain are optionally and independently replaced by —C(R 10 ) 2 —, —N(R)—, —N(R)C(O)—, —C(O)N(R)—, —N(R)S(O) 2 —, —S(O) 2 N(R)—, —(O)—, —C(O)—, —OC(O)—, —C(O)O—, —S—, —S(O)— or —S(O) 2 —; or

L 1 and one instance of R 7 are taken together with their intervening atoms to form a 5-10 membered partially unsaturated or aromatic ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, sulfur, and boron; wherein said ring is substituted by q instances of R 11 ; and R 5 is attached to any position of the ring formed by L 1 and R 7 ;

m is 0-4;

n is 0-4;

p is 0-6;

q is 0-4; and

each R is independently hydrogen, or an optionally substituted group selected from C 1-6 aliphatic, phenyl, a 4-7 membered saturated or partially unsaturated heterocyclic having 1-2 heteroatoms independently selected from nitrogen, oxygen, and sulfur, and a 5-6 membered heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, and sulfur, or:

two R groups on the same nitrogen are taken together with their intervening atoms to form a 4-7 membered saturated, partially unsaturated, or heteroaryl ring having 0-3 heteroatoms, in addition to the nitrogen, independently selected from nitrogen, oxygen, and sulfur.

2. The compound of claim 1 , wherein Ring A is phenyl, pyridin-2-yl, pyridine-3-yl, or pyrazol-4-yl.

3. The compound of claim 2 , wherein Ring A is pyridin-2-yl.

4. The compound of claim 1 , wherein X is ═C(R 6 )—; and Y is ═N—.

5. The compound of claim 4 , wherein R 6 is hydrogen.

6. The compound of claim 1 , wherein L 1 is —CH 2 C(O)—, —C(O)—, or a covalent bond.

7. The compound of claim 6 , wherein L 1 is a covalent bond.

8. The compound of claim 1 , wherein R 3 is phenyl, pyrrolidinyl, or piperidinyl.

9. The compound of claim 1 , wherein R 3 is phenyl.

10. The compound of claim 1 , wherein n is 2, and at least one R 8 is fluoro.

11. A compound selected from

I-1

I-2

I-3

I-4

I-5

I-6

I-7

I-8

I-9

I-10

I-12

I-13

I-14

I-15

I-16

I-17

I-18

I-19

I-20

I-21

I-22

I-23

I-24

I-25

I-26

I-27

I-28

I-29

I-30

I-31

I-32

I-33

I-34

I-35

I-36

I-37

I-38

I-39

I-40

I-41

I-42

I-43

I-44

I-45

I-46

I-47

I-48

I-49

I-50

I-51

I-52

I-53

I-54

I-55

I-56

I-57

I-58

I-59

I-60

I-61

I-62

I-63

I-64

I-65

I-66

I-67

I-68

I-69

I-70

I-71

I-72

I-73

I-74

I-75

I-76

I-77

I-78

I-79

I-80

I-81

I-82

I-83

I-84

I-85

I-86

I-87

I-88

I-89

I-90

I-91

I-92

I-93

or a pharmaceutically acceptable salt thereof.

12. A pharmaceutical composition comprising a compound according to claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant, or vehicle.

Assignments (13)
INTERCOMPANY AGREEMENT Recorded Sep 11, 2023
From: NIMBUS LAKSHMI, INC.
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 064867/0415 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2017
From: PHARMA-VATION CONSULTING LLC
To: NIMBUS DISCOVERY, INC.
Reel/Frame 043277/0563 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2017
From: WESTER, RONALD T.
To: NIMBUS DISCOVERY, INC.
Reel/Frame 043277/0575 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2017
From: HARRIMAN, GERALDINE C.
To: NIMBUS DISCOVERY, INC.
Reel/Frame 043277/0621 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2017
From: MASSE, CRAIG E.
To: NIMBUS DISCOVERY, INC.
Reel/Frame 043277/0660 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2017
From: NIMBUS DISCOVERY, INC.
To: NIMBUS LAKSHMI, INC.
Reel/Frame 043277/0694 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2017
From: ROMERO, DONNA L.
To: PHARMA-VATION CONSULTING LLC
Reel/Frame 043277/0547 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2017
From: SHELLEY, MEE
To: SCHRÖDINGER, INC.
Reel/Frame 043277/0755 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2017
From: KENNEDY-SMITH, JOSHUA JAHMIL
To: SCHRÖDINGER, INC.
Reel/Frame 043277/0778 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2017
From: DAHLGREN, MARKUS
To: SCHRÖDINGER, INC.
Reel/Frame 043277/0787 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2017
From: SCHRÖDINGER, INC.
To: SCHRÖDINGER, L.L.C.
Reel/Frame 043277/0829 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2017
From: SCHRÖDINGER, L.L.C.
To: NIMBUS DISCOVERY, INC.
Reel/Frame 043277/0866 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2017
From: GREENWOOD, JEREMY ROBERT
To: SCHRÖDINGER, INC.
Reel/Frame 043277/0739 →
Continuity (3)
Continuation 15054594 · Feb 26, 2016
Provisional Application 62126125 · Feb 27, 2015
Related Publication 20170305933A1 · Oct 26, 2017
Cited By (3)
US 12,221,453 US 12,233,062 US 12,509,463