Alcohol derivatives as Kv7 potassium channel openers for use in epilepsy or seizures

Patent metadata

Field	Value
Publication number	US-12508239-B2
Application number	US-202017631762-A
Country	US
Kind code	B2
Filing date	Jul 30, 2020
Priority date	Aug 2, 2019
Publication date	Dec 30, 2025
Grant date	Dec 30, 2025

Abstract

The present invention provides novel compounds (e.g., compounds of Formula I) which activate the Kv7 potassium channels. Separate aspects of the invention are directed to pharmaceutical compositions comprising said compounds and uses of the compounds to treat disorders responsive to the activation of Kv7 potassium channels.

First claim

The invention claimed is:

1 . A method of treating a patient in the need thereof suffering from epilepsy, epileptic syndromes, epileptic symptoms, treatment resistant or refractory epilepsy or seizures, comprising administering to the patient a therapeutically effective amount of a compound, or a pharmaceutically acceptable salt thereof, of Formula I:

wherein
R 1 is selected from the group consisting of C 1 -C 6 alkyl, CF 3 , CH 2 CF 3 , CF 2 CHF 2 , and C 3 -C 8 cycloalkyl, wherein said C 3 -C 8 cycloalkyl may be substituted with 1 or 2 F, CHF 2 or CF 3 , and R 2 is H, C 1 -C 6 alkyl or CF 3 ; or
R 1 and R 2 combine to form C 3 -C 5 cycloalkyl optionally substituted with 1 or 2 F, CHF 2 or CF 3 ;
R 3 is C 1 -C 3 alkyl or CH 2 O—C 1-3 alkyl, said C 1 -C 3 alkyl or CH 2 O—C 1-3 alkyl may optionally be substituted with 1 or 2 F; and
R 4 is selected from the group consisting of OCF 3 , OCH 2 CF 3 and OCHF 2 .

2 . A method of treating a patient in need thereof suffering from Focal (partial) epilepsy with simple partial seizures, Focal (partial) epilepsy with complex partial seizures, Generalized idiopathic epilepsy, Grand mal seizures, Status epilepticus, neonatal seizures, KCNQ epileptic encephalopathy (KCNQ2EE), Benign Familial Neonatal Convulsions, severe myoclonic epilepsy in infancy, epilepsy with continuous spike waves during slow-wave sleep, West syndrome, Lennox-Gastaut syndrome, Dravet syndrome and Early myoclonic encephalopathy, Ohtahara syndrome, or seizures related to stress, hormonal changes, drugs, alcohol, infection, traumatic brain injury, stroke, brain cancers, autism spectrum disorders or metabolic disturbances, hyponatraemia, or epileptic symptoms as part of Alzheimer's disease, Lewy body disease, Huntington's disease juvenile form, or fronto-temporal lobar degeneration, comprising administering to the patient a therapeutically effective amount of a compound, or a pharmaceutically acceptable salt thereof, of Formula I:

wherein
R 1 is selected from the group consisting of C 1 -C 6 alkyl, CF 3 , CH 2 CF 3 , CF 2 CHF 2 , and C 3 -C 8 cycloalkyl, wherein said C 3 -C 8 cycloalkyl may be substituted with 1 or 2 F, CHF 2 or CF 3 , and R 2 is H, C 1 -C 6 alkyl or CF 3 ; or
R 1 and R 2 combine to form C 3 -C 8 cycloalkyl optionally substituted with 1 or 2 F, CHF 2 or CF 3 ;
R 3 is C 1 -C 3 alkyl or CH 2 O—C 1-3 alkyl, said C 1 -C 3 alkyl or CH 2 O-C1-3 alkyl may optionally be substituted with 1 or 2 F; and
R 4 is selected from the group consisting of OCF 3 , OCH 2 CF 3 and OCHF 2 .

3 . A method for the manufacture of a medicament for treating epilepsy, epileptic syndromes, epileptic symptoms, treatment resistant or refractory epilepsy, or seizures, or Focal (partial) epilepsy with simple partial seizures, Focal (partial) epilepsy with complex partial seizures, Generalized idiopathic epilepsy, Grand mal seizures, Status epilepticus, neonatal seizures, KCNQ epileptic encephalopathy (KCNQ2EE), Benign Familial Neonatal Convulsions, severe myoclonic epilepsy in infancy, epilepsy with continuous spike waves during slow-wave sleep, West syndrome, Lennox-Gastaut syndrome, Dravet syndrome and Early myoclonic encephalopathy, Ohtahara syndrome, or epileptic symptoms as part of Alzheimer's disease, Lewy body disease, Huntington's disease juvenile form, or fronto-temporal lobar degeneration, comprising mixing a compound of Formula I with a pharmaceutically acceptable excipient:

wherein
R 1 is selected from the group consisting of C 1 -C 6 alkyl, CF 3 , CH 2 CF 3 , CF 2 CHF 2 , and C 3 -C 8 cycloalkyl, wherein said C 3 -C 8 cycloalkyl may be substituted with 1 or 2 F, CHF 2 or CF 3 , and R 2 is H, C 1 -C 6 alkyl or CF 3 ; or
R 1 and R 2 combine to form C 3 -C 5 cycloalkyl optionally substituted with 1 or 2 F, CHF 2 or CF 3 ;
R 3 is C 1 -C 3 alkyl or CH 2 O—C 1-3 alkyl, said C 1 -C 3 alkyl or CH 2 O—C 1-3 alkyl may optionally be substituted with 1 or 2 F; and
R 4 is selected from the group consisting of OCF 3 , OCH 2 CF 3 and OCHF 2 .

4 . The method according to claim 1 , wherein R 4 is OCF 3 or OCHF 2 .

5 . The method according to claim 1 , wherein R 2 is H or CH 3 .

6 . The method according to claim 1 , wherein R 3 is CH 2 O—C 1-3 alkyl.

7 . The method according to claim 1 , wherein R 1 is C 3 -C 4 cycloalkyl optionally substituted with 1 or 2 F, CHF 2 or CF 3 .

8 . The method according to claim 1 , wherein R 1 is t-butyl and R 2 is H.

9 . The method according to claim 1 , wherein R 1 and R 2 combine to form cyclobutyl optionally substituted with 1 or 2 F.

10 . The method according to claim 1 , wherein the compound is selected from the group consisting of:
(S)-3-hydroxy-4,4-dimethyl-N-[(1S)-1-[3-(trifluoromethoxy)phenyl]ethyl]pentanamide, (R)-3-hydroxy-4,4-dimethyl-N-[(1S)-1-[3-(trifluoromethoxy)phenyl]ethyl]pentanamide, (S)-3-hydroxy-4,4-dimethyl-N—((S)-1-(3-(2,2,2-trifluoroethoxy)phenyl)ethyl) pentanamide, (R)-3-hydroxy-4,4-dimethyl-N—((S)-1-(3-(2,2,2-trifluoroethoxy)phenyl)ethyl) pentanamide, (S)—N—((S)-1-(3-(difluoromethoxy)phenyl)ethyl)-3-hydroxy-4,4-dimethylpentanamide, (R)—N—((S)-1-(3-(difluoromethoxy)phenyl)ethyl)-3-hydroxy-4,4-dimethylpentanamide, (S)-3-hydroxy-4,4-dimthyl-N—((S)-1-(3-(trifluoromethyl)phenyl)ethyl) pentanamide (R)-3-hydroxy-4,4-dimethyl-N—((S)-1-(3-(trifluoromethyl)phenyl)ethyl) pentanamide, (S)-3-hydroxy-4,4-dimethyl-N—((S)-1-(3-(trifluoromethoxy)phenyl) propyl) pentanamide, (R)-3-hydroxy-4,4-dimethyl-N—((S)-1-(3-(trifluoromethoxy)phenyl) propyl) pentanamide, (S)-3-(3,3-difluorocyclobutyl)-3-hydroxy-N—((S)-1-(3-(trifluoromethoxy)phenyl)ethyl) propanamide, (R)-3-(3,3-difluorocyclobutyl)-3-hydroxy-N—((S)-1-(3-(trifluoromethoxy)phenyl)ethyl) propanamide, (S)-3-hydroxy-4-methyl-N—((S)-1-(3-(2,2,2-trifluoroethoxy)phenyl)ethyl) pentanamide, (R)-3-hydroxy-4-methyl-N—((S)-1-(3-(2,2,2-trifluoroethoxy)phenyl)ethyl) pentanamide, (S)-3-(1-(difluoromethyl)cyclopropyl)-3-hydroxy-N—((S)-1-(3-(trifluoro-methoxy)phenyl)ethyl) propanamide, (R)-3-(1-(difluoromethyl)cyclopropyl)-3-hydroxy-N—((S)-1-(3-(trifluoromethoxy)phenyl)ethyl) propanamide, (R)-3-hydroxy-N—((S)-1-(3-(trifluoromethoxy)phenyl)ethyl)-3-(1-(trifluoromethyl)cyclopropyl) propanamide, (S)-3-hydroxy-N—((S)-1-(3-(trifluoromethoxy)phenyl)ethyl)-3-(1-(trifluoromethyl)cyclopropyl) propanamide, (S)-3-hydroxy-4-methyl-N—((S)-1-(3-(trifluoromethoxy)phenyl)ethyl) pentanamide, (R)-3-hydroxy-4-methyl-N—((S)-1-(3-(trifluoromethoxy)phenyl)ethyl) pentanamide, N—((R)-2-(difluoromethoxy)-1-(3-(trifluoromethoxy)phenyl)ethyl)-3-(R)-hydroxy-4,4-dimethylpentanamide, N—((R)-2-(difluoromethoxy)-1-(3-(trifluoromethoxy)phenyl)ethyl)-3-(S)-hydroxy-4,4-dimethylpentanamide, (S)-3-hydroxy-N—((R)-2-methoxy-1-(3-(trifluoromethoxy)phenyl)ethyl)-4,4-dimethylpentanamide, (R)-3-hydroxy-N—((R)-2-methoxy-1-(3-(trifluoromethoxy)phenyl)ethyl)-4,4-dimethylpentanamide, (S)-2-(3,3-difluoro-1-hydroxycyclobutyl)-N-(1-(3-(trifluoromethoxy)phenyl)ethyl) acetamide, (S)-2-(1-hydroxycyclobutyl)-N-(1-(3-(2,2,2-trifluoroethoxy)phenyl)ethyl) acetamide, (3R)-3-hydroxy-4-methyl-N-[(1S)-1-[3-(2,2,2-trifluoroethoxy)phenyl]ethyl]-3-(trifluoromethyl) pentanamide, (3S)-3-hydroxy-4-methyl-N-[(1S)-1-[3-(2,2,2-trifluoroethoxy)phenyl]ethyl]-3-(trifluoromethy

Assignees

• H Lundbeck As

Inventors

• Sams Anette Graven
• Rottländer Mario
• Wang Xiaofang
• Das Debasis
• Hong Jian
• Chen Shu Hui
• Bastlund Jesper Frank
• Ivkovic Jelena
• Søby Karina Krøjer
• Larsen Morten Grupe

Classifications

• A61P25/08

  Antiepileptics; Anticonvulsants · CPC title

• C07B2200/07

  Optical isomers · CPC title

• C07C2601/02

  with a three-membered ring · CPC title

• C07C2601/04

  with a four-membered ring · CPC title

• C07C235/26

  the carbon skeleton being saturated and containing rings · CPC title