IP Library Granted Patent US 11,331,320
Granted Patent B2
US 11,331,320 · App. 16/821,624 · Granted May 17, 2022

Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors

Inventors: James D. Rodgers (Jupiter, FL); Stacey Shepard (Wilmington, DE)
Assignees: Incyte Holdings Corporation; Incyte Cororation
A61K31/519A61K9/0014A61K9/0053A61K9/20A61K31/573A61K45/06A61P17/04A61P29/00A61P35/04C07B59/002C07D417/04C07D471/04C07D487/04C07B2200/05
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Quick Facts
Patent No.
US 11,331,320
App. No.
16/821,624
Granted
May 17, 2022
Kind
B2
Abstract

The present invention provides heteroaryl substituted pyrrolo[2,3-b]pyridines and heteroaryl substituted pyrrolo[2,3-b]pyrimidines that modulate the activity of Janus kinases and are useful in the treatment of diseases related to activity of Janus kinases including, for example, immune-related diseases, skin disorders, myeloid proliferative disorders, cancer, and other diseases.

Claims (21)

1. A method of treating a disease selected from ulcerative colitis and Crohn's disease in a patient in need thereof, comprising administering to the patient a compound, which is 3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile, or a pharmaceutically acceptable salt thereof, wherein the treating refers to ameliorating or inhibiting ulcerative colitis and Crohn's disease in the patient.

2. The method of claim 1 , wherein the disease is ulcerative colitis.

3. The method of claim 1 , wherein the disease is Crohn's disease.

4. The method of claim 2 , wherein the compound is (3R)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile, or a pharmaceutically acceptable salt thereof.

5. The method of claim 2 , wherein the compound is (3R)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile.

6. The method of claim 3 , wherein the compound is (3R)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile, or a pharmaceutically acceptable salt thereof.

7. The method of claim 3 , wherein the compound is (3R)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile.

8. The method of claim 2 , wherein the compound is (3S)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile, or a pharmaceutically acceptable salt thereof.

9. The method of claim 2 , wherein the compound is (3S)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile.

10. The method of claim 3 , wherein the compound is (3S)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile, or a pharmaceutically acceptable salt thereof.

11. The method of claim 3 , wherein the compound is (3S)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile.

12. The method of claim 2 , wherein said administering comprises administering a pharmaceutical composition comprising the compound, or the pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

13. The method of claim 3 , wherein said administering comprises administering a pharmaceutical composition comprising the compound, or the pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

14. The method of claim 4 , wherein said administering comprises administering a pharmaceutical composition comprising the compound, or the pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

15. The method of claim 5 , wherein said administering comprises administering a pharmaceutical composition comprising the compound and a pharmaceutically acceptable carrier.

16. The method of claim 6 , wherein said administering comprises administering a pharmaceutical composition comprising the compound, or the pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

17. The method of claim 7 , wherein said administering comprises administering a pharmaceutical composition comprising the compound and a pharmaceutically acceptable carrier.

18. The method of claim 8 , wherein said administering comprises administering a pharmaceutical composition comprising the compound, or the pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

19. The method of claim 9 , wherein said administering comprises administering a pharmaceutical composition comprising the compound and a pharmaceutically acceptable carrier.

20. The method of claim 10 , wherein said administering comprises administering a pharmaceutical composition comprising the compound, or the pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

21. The method of claim 11 , wherein said administering comprises administering a pharmaceutical composition comprising the compound and a pharmaceutically acceptable carrier.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 19, 2020
From: RODGERS, JAMES D.; SHEPARD, STACEY
To: INCYTE CORPORATION
Reel/Frame 054091/0205 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 19, 2020
From: INCYTE CORPORATION
To: INCYTE HOLDINGS CORPORATION; INCYTE CORPORATION
Reel/Frame 054091/0267 →
Continuity (17)
Continuation 16177602 · Nov 1, 2018
Continuation 15960069 · Apr 23, 2018
Continuation 15356957 · Nov 21, 2016
Continuation 15233652 · Aug 10, 2016
Continuation 15173057 · Jun 3, 2016
Continuation 14711576 · May 13, 2015
Continuation 14274948 · May 12, 2014
Continuation 14020505 · Sep 6, 2013
Division 13076220 · Mar 30, 2011
Continuation 12549170 · Aug 27, 2009
Continuation 11637545 · Dec 12, 2006
Provisional Application 60859404 · Nov 16, 2006
Provisional Application 60856872 · Nov 3, 2006
Provisional Application 60850625 · Oct 10, 2006
Provisional Application 60810231 · Jun 2, 2006
Provisional Application 60749905 · Dec 13, 2005
Related Publication 20200338077A1 · Oct 29, 2020
Cited By (3)
US 12,428,426 US 12,440,495 US 12,479,851