IP Library Granted Patent US 9,908,886
Granted Patent B2
US 9,908,886 · App. 14/363,718 · Granted Mar 6, 2018

Bicyclic heterocyclic derivatives as MNK1 and MNK2 modulators and uses thereof

Inventors: Kassoum Nacro (Singapore, SG); Athisayamani Jeyaraj Duraiswamy (Singapore, SG); Lohitha Rao Chennamaneni (Singapore, SG)
Assignee: Agency for Science, Technology and Research
C07D487/04A61K31/4184A61K31/437A61K31/4545A61K31/496A61K31/4985A61K31/5025A61K31/519A61K31/5377A61K31/551A61K31/553A61K45/06C07D235/06C07D471/04C07D471/10C07D491/107C07D519/00A61K2201/094
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Quick Facts
Patent No.
US 9,908,886
App. No.
14/363,718
Granted
Mar 6, 2018
Kind
B2
Abstract

The present invention relates to certain compounds (e.g., imidazopyrazine, imidazopyridine, imidazopyridazine and imidazpyrimidine compounds) that act as inhibitors of the MAP kinase interacting kinases MNK2a, MNK2b, MNK1a, and MNK1b. The present invention further relates to pharmaceutical compositions comprising these compounds, and to the use of the compounds for the preparation of a medicament for the prophylaxis and treatment of diseases (e.g., proliferative diseases (e.g., cancer), inflammatory diseases, Alzheimer's disease), as well as methods of treating these diseases.

Claims (31)

1. A compound of Formula (Ib-i) or (Ib-ii):

or a pharmaceutically acceptable form thereof, wherein

X 1 , X 2 , and X 3 are independently N or C;

X 4 and X 5 are independently N or CR 4 ;

wherein at least one of X 1 ; X 2 , X 3 , X 4 , and X 5 is N;

X 7 is N or CH;

X 8 is N or CH;

is a single or double bond, as valency allows;

R 1 is —C(O)R, wherein R is an optionally substituted heterocyclyl;

R 2 , R 3 are independently —H, —F, —Cl, —CN, —CH 3 , —CF 3 , —CHF 2 , —C(O)NH 2 , —OH, —OC 1-4 alkyl, or —OCF 3 , and R 7 is H, —F, —Cl, —CN, —CH 3 , —CF 3 , —CHF 2 , —OH, —OC 1-4 alkyl, or —OCF 3 ;

R 6 is hydrogen, or R 6 and R 7 are taken together to form a 5-6 membered fused heterocyclyl or 5-6 membered fused heteroaryl; and

each R 4 is independently hydrogen or C 1-6 alkyl.

2. The compound of claim 1 , wherein R 7 is —CN.

3. The compound of claim 1 , wherein R 1 is —C(O)R, wherein R is one of the following:

4. The compound of claim 1 , wherein the compound is selected from the group consisting of:

and pharmaceutically acceptable forms thereof.

5. A composition comprising a compound of claim 1 , or a pharmaceutically acceptable form thereof, and a pharmaceutically acceptable excipient.

6. The composition of claim 5 , wherein the composition additionally comprises a kinase inhibitor.

7. The composition of claim 6 , wherein the kinase inhibitor is selected from a PI3K inhibitor or a mTOR inhibitor.

8. A compound of Formula (Ib-i) or (lb-ii):

or a pharmaceutically acceptable form thereof, wherein

X 1 , X 2 , and X 3 are independently N or C;

X 4 and X 5 are independently N or CR 4 ;

wherein at least one of X 1 , X 2 , X 3 , X 4 , and X 5 is N;

X 7 is N or CH;

X 8 is N or CH;

is a single or double bond, as valency allows;

R 1 is —C(O)R, wherein R is an optionally substituted heterocyclyl;

R 2 , R 3 , and R 6 are independently —H, —F, —Cl, —CN, —CH 3 , —CF 3 , —CHF 2 , —C(O)NH 2 , —OH, —OC 1-4 alkyl, or —OCF 3 ;

R 7 is independently —H, —F, —Cl, —CN, —CH 3 , —CF 3 , —CHF 2 , —OH, —OC 1-4 alkyl, or —OCF 3 ; or R 6 and R 7 are taken together to form a 5-6 membered fused heterocyclyl or 5-6 membered fused heteroaryl ring having 1-3 ring heteroatoms, wherein each heteroatom is nitrogen; and

each R 4 is independently hydrogen or C 1-6 alkyl.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 15, 2014
From: DURAISWAMY, ATHISAYAMANI JEYARAJ; NACRO, KASSOUM; CHENNAMANENI, LOHITHA RAO
To: AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH
Reel/Frame 033548/0737 →
Priority Claims (1)
GB 1205669.3 · Mar 30, 2012 · national
Continuity (1)
Related Publication 20140371199A1 · Dec 18, 2014