IP Library Granted Patent US 8,883,806
Granted Patent B2
US 8,883,806 · App. 13/761,771 · Granted Nov 11, 2014

Processes for preparing JAK inhibitors and related intermediate compounds

Inventor: Jiacheng Zhou (Newark, DE)
Assignee: Incyte Corporation
C07D487/04C07F7/1892C07F7/10
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Quick Facts
Patent No.
US 8,883,806
App. No.
13/761,771
Granted
Nov 11, 2014
Kind
B2
Abstract

The present invention is related to processes for preparing chiral substituted pyrazolyl pyrrolo[2,3-d]pyrimidines of Formula III, and related synthetic intermediate compounds. The chiral substituted pyrazolyl pyrrolo[2,3-d]pyrimidines are useful as inhibitors of the Janus Kinase family of protein tyrosine kinases (JAKs) for treatment of inflammatory diseases, myeloproliferative disorders, and other diseases.

Claims (16)

1. A process of preparing a composition comprising an enantiomeric excess of the (R)-enantiomer of a compound of Formula III′:

comprising:

(a) treating a compound of Formula XI′:

with sodium hydride and 2-(trimethylsilyl)ethoxymethyl chloride to form a compound of Formula X″:

(b) treating said compound of Formula X″ with a compound of Formula XIII′:

in the presence of Pd(triphenylphosphine) 4 , potassium carbonate, and a solvent, to form a compound of Formula XII″:

(c) reacting said compound of Formula XII″ under deprotection conditions to form a compound of Formula IV″:

(d) reacting said compound of Formula IV″ with a compound of Formula D-1′:

under conditions sufficient to form a composition comprising a racemate of a compound of Formula I″:

(e) passing said composition comprising said racemate of said compound of Formula I″ through a chiral chromatography unit using a mobile phase and collecting a composition comprising an enantiomeric excess of the (R)-enantiomer of said compound of Formula I″; and

(f) reacting said compound of Formula I″ with boron trifluoride diethyl etherate, followed by aqueous ammonium hydroxide to form a composition comprising an enantiomeric excess of the (R)-enantiomer of said compound of Formula III′;

wherein * is a chiral carbon.

2. A compound of Formula XII″, which is:

or a pharmaceutically acceptable salt thereof.

3. A composition comprising an enantiomeric excess of the (R)-enantiomer of a compound of Formula I″

or a pharmaceutically acceptable salt thereof.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE OMMISSION OF SECOND RECEIVING PARTY NAME PREVIOUSLY RECORDED AT REEL: 035292 FRAME: 0004. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jul 2, 2015
From: INCYTE CORPORATION
To: INCYTE HOLDINGS CORPORATION; INCYTE CORPORATION
Reel/Frame 036054/0696 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2015
From: INCYTE CORPORATION
To: INCYTE HOLDINGS CORPORATION AND INCYTE CORPORATION
Reel/Frame 035924/0004 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 7, 2014
From: ZHOU, JIACHENG; LIU, PINGLI; LIN, QIYAN; METCALF, BRIAN W.; MELONI, DAVID; PAN, YONGCHUN; XIA, MICHAEL; LI, MEI; YUE, TAI-YUEN; RODGERS, JAMES D.; WANG, HAISHENG
To: INCYTE CORPORATION
Reel/Frame 033250/0791 →
Continuity (3)
Division 12687623 · Jan 14, 2010
Provisional Application 61144991 · Jan 15, 2009
Related Publication 20130253191A1 · Sep 26, 2013