Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof

US9260422B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9260422-B2
Application numberUS-201214235253-A
CountryUS
Kind codeB2
Filing dateJul 26, 2012
Priority dateJul 28, 2011
Publication dateFeb 16, 2016
Grant dateFeb 16, 2016

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Certain chemical entities are provided herein. Also provided are pharmaceutical compositions comprising at least one chemical entity and one or more pharmaceutically acceptable vehicle. Methods of treating patients suffering from certain diseases and disorders responsive to the inhibition of KMO activity are described, which comprise administering to such patients an amount of at least one chemical entity effective to reduce signs or symptoms of the disease or disorder are disclosed. These diseases include neurodegenerative disorders such as Huntington's disease. Also described are methods of treatment include administering at least one chemical entity as a single active agent or administering at least one chemical entity in combination with one or more other therapeutic agents. Also provided are methods for screening compounds capable of inhibiting KMO activity.

First claim

Opening claim text (preview).

What is claimed: 1. At least one chemical entity chosen from compounds of Formula I and pharmaceutically acceptable salts thereof wherein: R 1 is chosen from optionally substituted aryl and optionally substituted heteroaryl; R 2 is tetrazolyl; R 3 is chosen from hydrogen and optionally substituted lower alkyl and R 4 is chosen from hydrogen, halo, optionally substituted lower alkyl, hydroxyl, optionally substituted lower alkoxy, and optionally substituted amino, or R 1 and R 4 , taken together with intervening atoms form a bicyclic ring of the formula which is optionally substituted where m is 0 or 1 and n is 0 or 1, provided that at least one of m and n is 1, provided that 1) when R 3 and R 4 are hydrogen, then R 1 is not 5-chloropyridin-3-yl, 3,5-dichlorophenyl, or where R 21 is halo and R 22 is hydrogen, halo, trifluoromethoxy, methyl, or isopropoxy. 2. At least one chemical entity of claim 1 wherein R 1 is phenyl optionally substituted with one, two, or three groups chosen from heteroaryl, heterocycloalkyl, cycloalkyl, optionally substituted cycloalkoxy, optionally substituted amino, halo, optionally substituted lower alkyl, optionally substituted lower alkoxy, and hydroxy. 3. At least one chemical entity of claim 2 wherein R 1 is phenyl optionally substituted with one, two, or three groups chosen from heteroaryl, heterocycloalkyl, cycloalkyl, cycloalkoxy optionally substituted with lower alkyl, lower alkoxy, or lower alkyl substituted with halo, optionally substituted amino, halo, lower alkyl optionally substituted with amino, alkylamino, dialkylamino, or heterocycloalkyl, trifluoromethyl, trifluoromethoxy, lower alkoxy, and hydroxy. 4. At least one chemical entity of claim 3 wherein R 1 is phenyl optionally substituted with one, two, or three groups chosen from furan-2-yl, 1H-pyrrol-2-yl, 1H-imidazol-2-yl, pyrrolidin-3-yl, pyrrolidin-1-yl, oxetan-3-yl optionally substituted with lower alkyl, halo, lower alkyl, cyclopropyl optionally substituted with lower alkyl, lower alkoxy, or lower alkyl substituted with halo, optionally substituted amino, lower alkyl optionally substituted with amino, alkylamino, dialkylamino, or heterocycloalkyl, trifluoromethoxy, cyclopropoxy optionally substituted with lower alkoxy, lower alkoxy, or lower alkyl substituted with halo, and trifluoromethyl. 5. At least one chemical entity of claim 4 wherein R 1 is chosen from 3-chloro-4-cyclopropoxyphenyl, 4-tert-butyl-3-chlorophenyl, 3-chloro-4-(furan-2-yl)phenyl, 3-chloro-4-(1H-pyrrol-2-yl)phenyl, 3-chloro-4-(1H-imidazol-2-yl)phenyl, 3-chloro-4-(pyrrolidin-3-yl)phenyl, 3-chloro-4-(pyrrolidin-1-yl)phenyl, 3-chloro-4-(3-methyloxetan-3-yl)phenyl, 3-chloro-4-[1-(trifluoromethyl)cyclopropyl]phenyl, 3-chloro-4-cyclopropylphenyl, 3-chloro-4-(1-methylcyclopropyl)phenyl, 3-chloro-4-(1-methoxycyclopropyl)phenyl, 3-chloro-4-[cyclopropyl(methyl)amino]phenyl, 3-chloro-4-(cyclopropylamino)phenyl, 3-chloro-4-[(dimethylamino)methyl]phenyl, 4-(aziridin-1-ylmethyl)-3-chlorophenyl, 3-chloro-4-trifluoromethoxyphenyl, 3-chloro-4-methylphenyl, 3-fluoro-4-methylphenyl, 3-chloro-4-fluorophenyl, 3-chloro-4-isopropoxyphenyl, 3,4-difluorophenyl, 2-trifluoromethylphenyl, 3,4-dichlorophenyl, 3-chlorophenyl, 4-chlorophenyl, and 3,5-dichlorophenyl. 6. At least one chemical entity of claim 1 wherein R 2 is chosen from 1H-tetrazol-5-yl, 2H-tetrazol-5-yl, and tetrazol-1-yl. 7. At least one chemical entity of claim 1 wherein R 4 is chosen from hydrogen, methyl, fluoro, methoxy, methoxymethyl, hydroxyl, and amino. 8. At least one chemical entity of claim 7 wherein R 4 is hydrogen. 9. At least one chemical entity of claim 1 wherein R 3 is hydrogen. 10. At least one chemical entity chosen from 4-(6-(3-chloro-4-isopropoxyphenyl)pyrimidin-4-yl)pyrrolidine-2-carboxylic acid, 4-(3,4-dichlorophenyl)-6-(4-(trifluoromethyl)-1H-imidazol-2-yl)pyrimidine, 4-(6-(3,4-dichlorophenyl)pyrimidin-4-yl)piperazine-2-carboxylic acid, (R)-1-(6-(3,4-dichlorophenyl)pyrimidin-4-yl)pyrrolidine-2-carboxylic acid, (S)-1-(6-(3,4-dichlorophenyl)pyrimidin-4-yl)pyrrolidine-2-carboxylic acid, 1-(6-(3,4-dichlorophenyl)pyrimidin-4-yl)pyrrolidine-3-carboxylic acid, 2-(6-(3-chloro-4-cyclopropoxyphenyl)pyrimidin-4-yl)oxazole, 1-(6-(3,4-dichlorophenyl)pyrimidin-4-yl)piperazine-2-carboxylic acid, 5-(6-(3-chloro-4-cyclopropoxyphenyl)pyrimidin-4-yl)pyrrolidine-2-carboxylic acid, 4-(3-chloro-4-cyclopropoxyphenyl)-6-(1H-1,2,3,4-tetrazol-5-yl)pyrimidine, 3-[6-(3-chloro-4-cyclopropoxyphenyl)pyrimidin-4-yl]-4,5-dihydro-1,2,4-oxadiazol-5-one, 4-[3-chloro-4-(oxetan-3-yloxy)phenyl]-6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidine, 3-{6-[3-chloro-4-(oxetan-3-yloxy)phenyl]pyrimidin-4-yl}-4,5-dihydro-1,2,4-oxadiazol-5-one, 4-[3-chloro-4-(cyclopropylmethoxy)phenyl]-6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidine, 3-{6-[3-chloro-4-(cyclopropylmethoxy)phenyl]pyrimidin-4-yl}-4,5-dihydro-1,2,4-oxadiazol-5-one, 4-[3-chloro-4-(cyclopropoxymethyl)phenyl]-6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidine, 3-{6-[3-chloro-4-(cyclopropoxymethyl)phenyl]pyrimidin-4-yl}-4,5-dihydro-1,2,4-oxadiazol-5-one, 4-[3-chloro-4-(cyclopropylmethyl)phenyl]-6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidine, 3-{6-[3-chloro-4-(cyclopropylmethyl)phenyl]pyrimidin-4-yl}-4,5-dihydro-1,2,4-oxadiazol-5-one, 4-[3-chloro-4-(cyclopropylsulfanyl)phenyl]-6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidine, 3-{6-[3-chloro-4-(cyclopropylsulfanyl)phenyl]pyrimidin-4-yl}-4,5-dihydro-1,2,4-oxadiazol-5-one, 4-[3-chloro-4-(cyclopropanesulfinyl)phenyl]-6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidine, 3-{6-[3-chloro-4-(cyclopropanesulfinyl)phenyl]pyrimidin-4-yl}-4,5-dihydro-1,2,4-oxadiazol-5-one, 4-[3-chloro-4-(cyclopropanesulfonyl)phenyl]-6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidine, 3-{6-[3-chloro-4-(cyclopropanesulfonyl)phenyl]pyrimidin-4-yl}-4,5-dihydro-1,2,4-oxadiazol-5-one, {2-chloro-4-[6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidin-4-yl]phenyl}(cyclopropyl)methanol, 3-{6-[3-chloro-4-(1-cyclopropoxyethyl)phenyl]pyrimidin-4-yl}-4,5-dihydro-1,2,4-oxadiazol-5-one, 4-(3-chloro-4-cyclopropanecarbonylphenyl)-6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidine, 3-[6-(3-chloro-4-cyclopropanecarbonylphenyl)pyrimidin-4-yl]-4,5-dihydro-1,2,4-oxadiazol-5-one, 4-(3-chloro-4-cyclopropylphenyl)-6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidine, 3-[6-(3-chloro-4-cyclopropylphenyl)pyrimidin-4-yl]-4,5-dihydro-1,2,4-oxadiazol-5-one, 4-[4-(aziridin-1-ylmethyl)-3-chlorophenyl]-6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidine, 3-{6-[4-(aziridin-1-ylmethyl)-3-chlorophenyl]pyrimidin-4-yl}-4,5-dihydro-1,2,4-oxadiazol-5-one, ({2-chloro-4-[6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidin-4-yl]phenyl}methyl)dimethylamine, 3-(6-{3-chloro-4-[(dimethylamino)methyl]phenyl}pyrimidin-4-yl)-4,5-dihydro-1,2,4-oxadiazol-5-one, 4-(7-chloro-1-benzofuran-5-yl)-6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidine, 3-[6-(7-chloro-1-benzofuran-5-yl)pyrimidin-4-yl]-4,5-dihydro-1,2,4-oxadiazol-5-one, 7-chloro-5-[6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidin-4-yl]-1,3-benzoxazole, 3-[6-(7-chloro-1,3-benzoxazol-5-yl)pyrimidin-4-yl]-4,5-dihydro-1,2,4-oxadiazol-5-one, 7-chloro-5-[6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidin-4-yl]-1,3-benzothiazole 3-[6-(7-chloro-1,3-benzothiazol-5-yl)pyrimidin-4-yl]-4,5-dihydro-1,2,4-oxadiazol-5-one 7-chloro-5-[6-(2H-1,2,3,4-tetrazol-5-yl)pyrimidin-4-yl]-1H-1,3-benzodiazole, 3-[6-(7-chloro-1H-1,3-benzodiazol-5-yl)pyrimidin-4-yl]-4,5-dihydro-1,2,4-oxadiazol-5-one,

Assignees

Inventors

Classifications

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

  • for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis · CPC title

  • for treating abnormal movements, e.g. chorea, dyskinesia · CPC title

  • Anti-Parkinson drugs · CPC title

  • for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia · CPC title

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What does patent US9260422B2 cover?
Certain chemical entities are provided herein. Also provided are pharmaceutical compositions comprising at least one chemical entity and one or more pharmaceutically acceptable vehicle. Methods of treating patients suffering from certain diseases and disorders responsive to the inhibition of KMO activity are described, which comprise administering to such patients an amount of at least one chem…
Who is the assignee on this patent?
Dominguez Celia, Toledo-Sherman Leticia M, Courtney Stephen Martin, and 6 more
What technology area does this patent fall under?
Primary CPC classification C07D239/42. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).