IP Library Granted Patent US 10,189,813
Granted Patent B2
US 10,189,813 · App. 15/561,189 · Granted Jan 29, 2019

Formylated N-heterocyclic derivatives as FGFR4 inhibitors

Inventors: Nicole Buschmann (Basel, CH); Robin Alec Fairhurst (Basel, CH); Pascal Furet (Thann, FR); Thomas Knoepfel (Rheinfelden, CH); Catherine Leblanc (Basel, CH); Robert Mah (Muttenz, CH)
Assignee: NOVARTIS AG
C07D401/12A61K31/4427C07D213/75C07D401/14C07D405/14
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Quick Facts
Patent No.
US 10,189,813
App. No.
15/561,189
Granted
Jan 29, 2019
Kind
B2
Abstract

The present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof; a method for manufacturing said compound, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition comprising said compound.

Claims (50)

1. A compound of formula (I) in free form or in pharmaceutically acceptable salt form

wherein

X is N or CH;

A is C(O) and B is NR 5 or

A and B together form part of a 5- or 6-membered aromatic ring wherein A is C and B is C or N;

R 1 is selected from hydrogen, hydroxyC 1 -C 3 alkyl, haloC 1 -C 3 alkyl, CO 2 H, CH 2 NR 2 R 3 , a 5-membered aromatic heterocyclic ring comprising at least one heteroatom selected from N, O or S, which ring is optionally substituted once or more than once with C 1 -C 3 alkyl;

R 2 is C 1 -C 3 alkyl and R 3 is C(O)C 1 -C 3 alkyl

or

R 2 and R 3 together with the N to which they are attached form a saturated 5- or 6-membered ring optionally comprising one additional heteroatom selected from N, O or S, which ring is optionally substituted once or more than once with R 4 ;

R 4 is for each occurrence independently selected from C 1 -C 3 alkyl, C 1 -C 3 alkoxy or two R 4 attached at the same carbon atom form an oxo group;

R 5 is selected from hydrogen, C 1 -C 3 alkyl, C 1 -C 3 alkoxyC 1 -C 3 alkyl, (CH 2 ) 0-1 —R 6 ;

R 6 is a 4-, 5-, or 6-membered saturated heterocyclic ring comprising at least one heteroatom selected from N, O, or S;

R 7 is selected from cyano, haloC 1 -C 3 alkyl;

R 8 is selected from hydrogen, NR 9 R 10 , C 1 -C 6 alkoxy;

R 9 is hydrogen;

R 10 is selected from C 1 -C 6 alkyl, hydroxyC 1 -C 6 alkyl, C 1 -C 4 alkoxyC 1 -C 6 alkyl.

2. A compound according to claim 1 of formula (Ia) in free form or in pharmaceutically acceptable salt form

3. A compound according to claim 1 of formula (Ib) in free form or in pharmaceutically acceptable salt form

wherein n is 0 or 1;

B is C or N;

D, E, F, G are each independently selected from CH or N, provided that when n is 0, at least one of B, E, F or G is N.

4. A compound according to claim 1 in free form or in pharmaceutically acceptable salt form wherein X is CH.

5. A compound according to claim 1 in free form or in pharmaceutically acceptable salt form which is selected from

6-((2-(6-formylpyridin-2-yl)phenyl)amino)nicotinonitrile;

3-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-1-(6-formylpyridin-2-yl)-1-methylurea;

3-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-1-(6-formylpyridin-2-yl)-1-(2-methoxyethyl)urea;

3-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-1-(6-formylpyridin-2-yl)-1-((tetrahydrofuran-3-yl)methyl)urea;

3-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-1-(6-formyl-5-(hydroxymethyl)pyridin-2-yl)-1-((tetrahydrofuran-3-yl)methyl)urea;

3-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-1-ethyl-1-(6-formyl-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)urea;

3-(5-cyano-4-(isopropylamino)pyridin-2-yl)-1-ethyl-1-(6-formyl-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)urea;

3-(5-cyano-4-isopropoxypyridin-2-yl)-1-ethyl-1-(6-formyl-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)urea;

3-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-1-methyl-1-(6-formyl-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)-1-methylurea;

3-(5-cyano-4-(isopropylamino)pyridin-2-yl)-1-(6-formyl-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)-1-methylurea;

N-((6-(3-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-1-methylureido)-2-formylpyridin-3-yl)methyl)-N-methylacetamide;

3-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-1-(5-(difluoromethyl)-6-formylpyridin-2-yl)-1-methylurea;

3-(5-cyano-4-isopropoxypyridin-2-yl)-1-(6-formyl-5-((4-methylpiperazin-1-yl)methyl)pyridin-2-yl)-1-methylurea;

3-(5-cyano-4-isopropoxypyridin-2-yl)-1-(5-(difluoromethyl)-6-formylpyridin-2-yl)-1-methylurea;

3-(5-cyanopyridin-2-yl)-1-(6-formyl-5-((2-oxopyrrolidin-1-yl)methyl)pyridin-2-yl)-1-methylurea;

3-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-1-(6-formyl-5-((2-oxopyrrolidin-1-yl)methyl)pyridin-2-yl)-1-methylurea;

3-(5-cyano-4-isopropoxypyridin-2-yl)-1-(6-formyl-5-((4-methyl-2-oxopiperazin-1-yl)methyl)pyridin-2-yl)-1-methylurea;

3-(5-cyano-4-((2-hydroxy-2-methylpropyl)amino)pyridin-2-yl)-1-(6-formyl-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)-1-methylurea;

3-(5-cyano-4-isopropoxypyridin-2-yl)-1-(6-formyl-5-((2-oxopyrrolidin-1-yl)methyl)pyridin-2-yl)-1-methylurea;

3-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-1-(6-formyl-5-((4-methyl-2-oxopiperazin-1-yl)methyl)pyridin-2-yl)-1-methylurea;

3-(5-cyano-4-isopropoxypyridin-2-yl)-1-(6-formyl-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)-1-methylurea;

3-(5-cyano-4-isopropoxypyridin-2-yl)-1-(6-formyl-5-((3-methoxypyrrolidin-1-yl)methyl)pyridin-2-yl)-1-methylurea;

6-(2-((4-((2-methoxyethyl)amino)-5-(trifluoromethyl)pyridin-2-yl)amino)-1H-imidazol-1-yl)-3-(1-methyl-1H-pyrazol-4-yl)picolinaldehyde;

6-(5-((4-((2-methoxyethyl)amino)-5-(trifluoromethyl)pyridin-2-yl)amino)-1H-pyrazol-1-yl)-3-(1-methyl-1H-pyrazol-4-yl)picolinaldehyde;

3-(5-cyano-4-isopropoxypyridin-2-yl)-1-(6-formyl-5-(pyrrolidin-1-ylmethyl)pyridin-2-yl)-1-methylurea and

1-(5-cyano-4-isopropoxypyridin-2-yl)-3-(4-formylpyrimidin-2-yl) urea.

6. A pharmaceutical composition comprising a therapeutically effective amount of a compound according to claim 1 or a pharmaceutically acceptable salt thereof and one or more pharmaceutically acceptable carriers.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2019
From: BUSCHMANN, NICOLE; FAIRHURST, ROBIN ALEC; FURET, PASCAL; KNOEPFEL, THOMAS; LEBLANC, CATHERINE; MAH, ROBERT
To: NOVARTIS PHARMA AG
Reel/Frame 050626/0810 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2019
From: NOVARTIS PHARMA AG
To: NOVARTIS AG
Reel/Frame 050626/0934 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 26, 2017
From: BUSCHMANN, NICOLE; FAIRHURST, ROBIN ALEC; FURET, PASCAL; KNOEPFEL, THOMAS; LEBLANC, CATHERINE; MAH, ROBERT
To: NOVARTIS PHARMA AG
Reel/Frame 043953/0460 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 26, 2017
From: NOVARTIS PHARMA AG
To: NOVARTIS AG
Reel/Frame 043953/0509 →
Priority Claims (1)
EP 15160735 · Mar 25, 2015 · regional
Continuity (1)
Related Publication 20180065951A1 · Mar 8, 2018