Bicyclic heterocycle compounds and their uses in therapy

Patent metadata

Field	Value
Publication number	US-9617283-B2
Application number	US-201314436345-A
Country	US
Kind code	B2
Filing date	Oct 18, 2013
Priority date	Oct 19, 2012
Publication date	Apr 11, 2017
Grant date	Apr 11, 2017

Abstract

The invention relates to new bicyclic heterocycle compounds, to pharmaceutical compositions comprising the compounds and to the use of the compounds in the treatment of diseases, e.g. cancer.

First claim

The invention claimed is:

1. A compound of formula (I):

or a tautomeric or stereochemically isomeric form, N-oxide, pharmaceutically acceptable salt or solvate thereof;
wherein
X is CH and Y is CR 9 , or one of X and Y is CR 9 and the other is nitrogen, or X and Y are nitrogen;
V is selected from NR 3 , CR 4a R 4b and O;
W is either absent or selected from CR 6 R 7 , CH 2 —CH 2 , O—CH 2 , CH 2 —O, C═O, SO 2 , O, NR 8 , CH 2 —NR 8 and NR 8 —CH 2 ;
when W is absent and V is CR 4a R 4b then the dotted bonds can join to form a single or double bond (in the latter case R 2a and R 4a are absent) otherwise the dotted bonds both represent a single bond;
when W is CH 2 —CH 2 , O—CH 2 , CH 2 —O, C═O, SO 2 , NR 8 , CH 2 —NR 8 or NR 8 —CH 2
then R 1a , R 1b , R 2a , R 2b , R 4a and R 4b are independently selected from hydrogen, halogen, C 1-4 alkyl, carboxyl, hydroxyl, hydroxyC 1-4 alkyl, C 1-4 alkyoxy, C 3-6 cycloalkyl, haloC 1-4 alkyl, methoxymethyl and nitrile,
or R 2a and R 2b , or R 4a and R 4b can together represent ═O,
or R 1a and R 1b , or R 2a and R 2b , or R 4a and R 4b can join together to form cyclopropyl or oxetanyl,
or R 1a or R 1b and R 4a or R 4b , or R 1a or R 1b and R 2a or R 2b , or R 2a or R 2b and R 4a or R 4b can join together to form a C 1-4 bridged alkyl group;
when W is CR 6 R 7 or O
then R 1a , R 1b , R 2a , R 2b , R 4a and R 4b are independently selected from hydrogen, halogen, C 1-4 alkyl, carboxyl, hydroxyl, hydroxyC 1-4 alkyl, C 1-4 alkyoxy, C 3-6 cycloalkyl, haloC 1-4 alkyl, methoxymethyl and nitrile,
or R 2a and R 2b , or R 4a and R 4b can together represent ═O,
or R 1a and R 1b , R 2a and R 2b , or R 4a and R 4b can join together to form cyclopropyl or oxetanyl,
or R 1a or R 1b and R 4a or R 4b , or R 1a or R 1b and R 2a or R 2b , or R 2a or R 2b and R 4a or R 4b can join together to form a C 1-4 bridged alkyl group,
provided that when X and Y are other than both nitrogen
R 1a , R 1b , R 2a , R 2b , R 4a and R 4b are not all hydrogen except when W is CR 6 R 7 , V is CR 4a R 4b , X is CH, Y is nitrogen and R 5 is other than 2,4-difluorobenzyl;

when W is absent
then R 1a , R 1b , R 2a , R 2b , R 4a and R 4b are independently selected from hydrogen, halogen, C 1-4 alkyl, carboxyl, hydroxyl, hydroxyC 1-4 alkyl, C 1-4 alkyoxy, C 3-6 cycloalkyl, haloC 1-4 alkyl, methoxymethyl and nitrile,
or R 2a and R 2b , or R 4a and R 4b can together represent ═O,
or R 1a and R 1b , or R 2a and R 2b , or R 4a and R 4b can join together to form cyclopropyl or oxetanyl,
or R 1a or R 1b and R 4a or R 4b , or R 1a or R 1b and R 2a or R 2b , or R 2a or R 2b and R 4a or R 4b can join together to form a C 1-4 bridged alkyl group,
or R 2a/2b and R 4a/4b can join together to form a fused phenyl or pyridinyl group which can be optionally substituted by one or more substituents R 10 ,
provided that
R 1a , R 1b , R 2a , R 2b , R 4a and R 4b are not all hydrogen,
where V is O and X and Y are other than both nitrogen, then R 1a , R 1b , R 2a and R 2b are not all hydrogen;

R 5 is selected from: benzyl optionally substituted on the phenyl group by one or two substituents selected from fluorine and nitrile, and optionally substituted on the methylene by hydroxyl; and C 2-4 alkyl substituted by one or two substituents selected from fluorine and hydroxyl;
R 6 and R 7 are independently selected from hydrogen, hydroxyl and fluorine;
R 3 and R 8 are independently selected from hydrogen, C 1-4 alkyl, —SO 2 —C 1-4 alkyl, —SO 2 —NH(C 1-4 alkyl), —SO 2 —N(C 1-4 alkyl) 2 , —C(═O)—NH—SO 2 —C 1-4 alkyl, —C(═O)—NH—SO 2 -phenyl, —C(═O)—N(C 1-4 alkyl) 2 , pyrimidinyl, —C(═O)-phenyl, —C(═O)—C 3-6 cycloalkyl and —C(═O)—C 1-4 alkyl, wherein the alkyl or cyclic groups can be optionally substituted by one or more substituents R 10 ;
R 9 is selected from hydrogen and nitrile; and
R 10 is independently selected from hydrogen, halogen, C 1-4 alkyl, carboxyl, hydroxyl, hydroxyC 1-4 alkyl, C 1-4 alkyoxy, C 3-6 cycloalkyl, haloC 1-4 alkyl, methoxymethyl and nitrile.

2. A compound as defined in claim 1 , wherein X and Y are both nitrogen; X is nitrogen and Y is CH; or X is CH and Y is nitrogen,
or a tautomeric or stereochemically isomeric form, N-oxide, pharmaceutically acceptable salt or solvate thereof.

3. A compound as defined in claim 2 , wherein X is nitrogen and Y is CH,
or a tautomeric or stereochemically isomeric form, N-oxide, pharmaceutically acceptable salt or solvate thereof.

4. A compound as defined in claim 2 , wherein X and Y are both nitrogen,
or a tautomeric or stereochemically isomeric form, N-oxide, pharmaceutically acceptable salt or solvate thereof.

5. A compound as defined in claim 1 , wherein W is either absent or selected from CR 6 R 7 , OCH 2 , CH 2 O, O and NR 8 ,
or a tautomeric or stereochemically isomeric form, N-oxide, pharmaceutically acceptable salt or solvate thereof.

6. A compound as defined in claim 5 , wherein W is absent or O,
or a tautomeric or stereochemically isomeric form, N-oxide, pharmaceutically acceptable salt or solvate thereof.

7. A compound as defined in claim 1 , wherein V is selected from CR 4a R 4b and O,
or a tautomeric or stereochemically isomeric form, N-oxide, pharmaceutically acceptable salt or solvate thereof.

8. A compound as defined in claim 7 , wherein V is CR 4a R 4b ,
or a tautomeric or stereochemically isomeric form, N-oxide, pharmaceutically acceptable salt or solvate thereof.

9. A compound as defined in claim 1 , wherein R 1a , R 1b , R 2a , R 2b , R 4a and R 4b are independently selected from hydrogen, halogen, C 1-4 alkyl, carboxyl, hydroxyl, hydroxyC 1-4 alkyl, C 1-4 alkyoxy, C 3-6 cycloalkyl, haloC 1-4 alkyl, methoxymethyl and nitrile, or a tautomeric or stereochemically isomeric form, N-oxide, pharmaceutically acceptable salt or solvate thereof.

10. A compound as defined in claim 9 , wherein R 1a , R 1b , R 2a , R 2b , R 4a and R 4b are independently selected from hydrogen and methyl,
or a tautomeric or stereochemically isomeric form, N-oxide, pharmaceutically acceptable salt or solvate thereof.

11. A compound as defined in claim 10 , wherein R 1a , R 1b , R 2b , R 4a and R 4b are all hydrogen and R 2a represents methyl,
or a tautomeric or stereochemically isomeric form, N-oxide, pharmaceutically acceptable salt or solvate thereof.

12. A compound as defined in claim 1 , wherein when W is absent and V represents CR 4a R 4b :
the dotted bonds join to form a single or a double bond;
R 1a and R 1b both represent hydrogen;
R 2a and R 2b both represent hydrogen or C 1-4 alkyl or one represents hydrogen and the other represents C 1-4 alkyl or R 2a and R 2b join together to form oxetanyl;
R 4a and R 4b both represent hydrogen, halogen or C 1-4 alkyl or one represents hydrogen and the other represents C 1-4 alkyl; or
R 2a/2b and R 4a/4b join together to form a fused unsubstituted phenyl or pyridinyl group; or
R 1a or 1b and R 4a or 4b join together to form a C 1-4 bridged alkyl group,
or a tautomeric or stereochemically isomeric form, N-oxide, pharmaceutically acceptable salt or solvate thereof.

13. A compound as defined in claim 1 , wherein when W is absent and V represents O:
R 1a and R 1

Assignees

• Astex Therapeutics Ltd

Inventors

• Chessari Gianni
• Johnson Christopher Norbert
• Page Lee William
• Buck Ildiko Maria
• Day James Edward Harvey
• Howard Steven
• Saxty Gordon
• Murray Christopher William
• Hopkins Anna

Classifications

• A61P35/00

  Antineoplastic agents · CPC title

• A61P3/10

  for hyperglycaemia, e.g. antidiabetics · CPC title

• A61P35/02

  specific for leukemia · CPC title

• A61P31/18

  for HIV · CPC title

• A61P37/02

  Immunomodulators · CPC title