Treating diseases mediated by blockade of the epithelial sodium channel with pyrazine-2-carboxamide derivatives

Patent metadata

Field	Value
Publication number	US-9643983-B2
Application number	US-201514847262-A
Country	US
Kind code	B2
Filing date	Sep 8, 2015
Priority date	Dec 10, 2007
Publication date	May 9, 2017
Grant date	May 9, 2017

Abstract

A compound of Formula I

in free or salt or solvate form, where R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 and R 11 have the meanings as indicated in the specification, is useful for treating diseases which respond to the blockade of the epithelial sodium channel. Pharmaceutical compositions that contain the compounds and processes for preparing the compounds are also described.

First claim

The invention claimed is:

1. A compound according to formula 2

wherein [LINKER] is selected from C 1 -C 6 alkylene, C 2 -C 6 alkenylene, C 2 -C 6 alkynylene, a 5- to 10-membered carbocyclic group, aryl, and a 5- to 10-membered heterocyclic group containing one or more heteroatoms selected from N, O and S, the ring systems being optionally substituted by one or more Z 1 groups; and
Z 1 is independently selected from OH, aryl, O-aryl, benzyl, O-benzyl, C 1 -C 6 alkyl optionally substituted by one or more OH groups, C 1 -C 6 alkyl optionally substituted by one or more halogen atoms, C 1 -C 6 alkoxy optionally substituted by one or more OH groups or C 1 -C 4 alkoxy, NR 19 (SO 2 )R 21 , (SO 2 )NR 19 R 20 , (SO 2 )R 20 , NR 19 C(O)R 20 , C(O)NR 19 R 20 , NR 19 C(O)NR 20 R 18 , NR 19 C(O)OR 20 , NR 19 R 21 , C(O)OR 19 , C(O)R 19 , SR 19 , OR 19 , oxo, CN, NO 2 , and halogen;
R 18 and R 20 are each independently selected from H and C 1 -C 6 alkyl;
R 19 and R 21 are each independently selected from H; C 1 -C 8 alkyl; C 3 -C 8 cycloalkyl; C 1 -C 4 alkoxy-C 1 -C 4 alkyl; (C 0 -C 4 alkyl)-aryl optionally substituted by one or more groups selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy and halogen; (C 0 -C 4 alkyl)- 3- to 14-membered heterocyclic group, the heterocyclic group including one or more heteroatoms selected from N, O and S, optionally substituted by one or more groups selected from halogen, oxo, C 1 -C 6 alkyl and C(O)C 1 -C 6 alkyl; (C 0 -C 4 alkyl)-O-aryl optionally substituted by one or more groups selected from C 1 -C 6 alkyl, C 1 -C 6 alkoxy and halogen; and (C 0 -C 4 alkyl)-O-3- to 14-membered heterocyclic group, the heterocyclic group including one or more heteroatoms selected from N, O and S, optionally substituted by one or more groups selected from halogen, C 1 -C 6 alkyl and C(O)C 1 -C 6 alkyl; wherein the alkyl groups are optionally substituted by one or more halogen atoms, C 1 -C 4 alkoxy, C(O)NH 2 , C(O)NHC 1 -C 6 alkyl or C(O)N(C 1 -C 6 alkyl) 2 ; or
R 19 and R 20 together with the nitrogen atom to which they attached form a 5- to 10-membered heterocyclic group, the heterocyclic group including one or more further heteroatoms selected from N, O and S, the heterocyclic group being optionally substituted by one or more substituents selected from OH; halogen; aryl; 5- to 10-membered heterocyclic group including one or more heteroatoms selected from N, O and S; S(O) 2 -aryl; S(O) 2 —C 1 -C 6 alkyl; C 1 -C 6 alkyl optionally substituted by one or more halogen atoms; C 1 -C 6 alkoxy optionally substituted by one or more OH groups or C 1 -C 4 alkoxy; and C(O)OC 1 -C 6 alkyl, wherein the aryl and heterocyclic substituent groups are themselves optionally substituted by C 1 -C 6 alkyl, C 1 -C 6 haloalkyl or C 1 -C 6 alkoxy; or a pharmaceutically acceptable salt thereof.

2. The compound according to claim 1 wherein R 18 , R 19 and R 20 are each independently selected from H and C 1 -C 6 alkyl; and
R 21 is selected from C 1 -C 8 alkyl, aryl and a 3- to 14-membered heterocyclic group; or a pharmaceutically acceptable salt thereof.

3. The compound according to claim 1 selected from the group consisting of:

or a pharmaceutically acceptable salt thereof.

4. A pharmaceutical composition comprising a compound according claim 1 , together with one or more pharmaceutical excipients.

5. A method for the treatment of a disease mediated by the blockade of an epithelial sodium channel consisting of cystic fibrosis, primary ciliary dyskinesia, chronic bronchitis, chronic obstructive pulmonary disease, asthma and respiratory tract infections comprising administration of a compound according to claim 1 or a pharmaceutically acceptable salt thereof.

6. A pharmaceutical combination of a compound according to claim 1 with an anti-inflammatory, bronchodilatory, antihistamine or anti-tussive drug substance.

Assignees

• Bhalay Gurdip
• Budd Emma
• Bloomfield Graham Charles
• Collingwood Stephen Paul
• Dunstan Andrew
• Edwards Lee
• Gedeck Peter
• Howsham Catherine
• Hunt Peter
• Hunt Thomas Anthony
• Oakley Paul
• Smith Nichola
• Novartis Ag

Inventors

• Bhalay Gurdip
• Budd Emma
• Bloomfield Graham Charles
• Collingwood Stephen Paul
• Dunstan Andrew
• Edwards Lee
• Gedeck Peter
• Howsham Catherine
• Hunt Peter
• Hunt Thomas Anthony
• Oakley Paul
• Smith Nichola

Classifications

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P37/00

  Drugs for immunological or allergic disorders · CPC title

• A61P37/08

  Antiallergic agents (antiasthmatic agents A61P11/06; ophthalmic antiallergics A61P27/14) · CPC title

• A61P29/00

  Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] · CPC title

• A61P31/00

  Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics · CPC title