Thiadiazine derivatives

US2021267993A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2021267993-A1
Application numberUS-201917259975-A
CountryUS
Kind codeA1
Filing dateJul 12, 2019
Priority dateJul 13, 2018
Publication dateSep 2, 2021
Grant date

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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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Abstract

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The invention relates to thiadiazine derivatives, or pharmaceutically acceptable salts, biologically active metabolites, pro-drugs, racemates, enantiomers, diastereomers, solvates and hydrates thereof, as well as to pharmaceutical compositions containing them and to their use as modulators of α7 nicotinic acetylcholine receptor activity in a mammalian subject Formula (I):

First claim

Opening claim text (preview).

1 . A compound of formula (I), wherein A is saturated, unsaturated or aromatic, monocyclic or bycyclic, fused or bridged carbocyclyl, or a saturated, unsaturated or aromatic monocyclic or bycyclic, fused or bridged heterocyclyl, optionally substituted by one or more halogen atom or halogen atoms, C 1-6 alkyl, C 1-6 alkoxy, or haloC 1-6 alkyl; B is saturated, unsaturated or aromatic, monocyclic or bycyclic, fused or bridged carbocyclyl, or a saturated, unsaturated or aromatic monocyclic or bycyclic, fused or bridged heterocyclyl, optionally substituted by one or more halogen atom or halogen atoms, C 1-6 alkyl, C 1-6 alkoxy, haloC 1-6 alkyl, CN, C(O)C 1-6 alkyl, or haloC 1-6 alkoxy; R 1 is C 1-6 alkyl, C 1-6 alkenyl, haloC 1-6 alkyl, C 3-8 cycloalkylC 1-6 alkyl, C 1-6 alkoxyC 1-6 alkyl, or C 4-6 heterocyclyl; or pharmaceutically acceptable salts, biologically active metabolites, pro-drugs, racemates, enantiomers, diastereomers, solvates and hydrates thereof. 2 . The compound according to claim 1 , wherein A is an optionally substituted saturated, unsaturated or aromatic, 4-9 membered monocyclic or bycyclic, fused or bridged carbocyclyl, or a saturated, unsaturated or aromatic 4-9 membered monocyclic or bycyclic, fused or bridged heterocyclyl containing 1-3 heteroatoms selected from the group of nitrogen, and oxygen; B is an optionally substituted saturated, unsaturated or aromatic, 4-9 membered monocyclic or bycyclic, fused or bridged carbocyclyl, or a saturated, unsaturated or aromatic 4-9 membered monocyclic or bycyclic, fused or bridged heterocyclyl containing 1-3 heteroatoms selected from the group of nitrogen, and oxygen; R 1 is C 1-6 alkyl, C 1-6 alkenyl, haloC 1-6 alkyl, C 3-8 cycloalkylC 1-6 alkyl, C 1-6 alkoxyC 1-6 alkyl, or C 4-6 heterocyclyl. 3 . The compound according to any one of claims 1 or 2 , wherein A is an optionally substituted cyclopentenyl, cyclohexyl, phenyl, cycloheptyl, bicyclo[3.1.0]hexanyl or indazolyl; B is an optionally substituted phenyl, pyridyl, pyrazyl, pyrazinyl, pyrimidinyl, benzodioxolyl, 1,2,3,4-tetrahydro-isoquinolinyl, or pyrazolo[1,5-a]pyridinyl; R1 is CH 3 , C 2 H 5 , nPr, iPr, nBu, secBu, allyl, —CH 2 —CF 3 , —CH 2 -cBu, —CH 2 -cPr, —C 2 H 5 —O—CH 3 , or tetrahydrofuryl. 4 . The compound according to any one of claims 1 to 3 , selected from the group of: 5-(3,4-dimethoxyphenyl)-2-methyl-N-(3-methylphenyl)-1,1-dioxo-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-(1,3-dimethyl-1H-indazol-5-yl)-2-methyl-N-(3-methylphenyl)-1,1-dioxo-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-(3,4-dimethoxyphenyl)-2-ethyl-N-(3-methylphenyl)-1,1-dioxo-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-(3,4-dimethoxyphenyl)-2-ethyl-1,1-dioxo-N-[6-(trifluoromethyl)pyridin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 2-ethyl-5-[4-methoxy-3-(trifluoromethyl)phenyl]-N-(3-methoxyphenyl)-1,1-dioxo-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 2-ethyl-5-[4-methoxy-3-(trifluoromethyl)phenyl]-N-(4-methoxyphenyl)-1,1-dioxo-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 2-ethyl-1,1-dioxo-5-[(1r,4r)-4-(trifluoromethyl)cyclohexyl]-N-[6-(trifluoromethyl)pyridin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; N-(6-cyanopyridin-2-yl)-2-ethyl-1,1-dioxo-5-[(1r,4r)-4-(trifluoromethyl)cyclohexyl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-(3,4-dimethoxyphenyl)-1,1-dioxo-2-(propan-2-yl)-N-[6-(trifluoromethyl)pyridin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-(3,4-dimethoxyphenyl)-1,1-dioxo-2-propyl-N-[3-(trifluoromethyl)phenyl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-(3,4-dimethoxyphenyl)-1,1-dioxo-2-propyl-N-[6-(trifluoromethyl)pyridin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-[4-methoxy-3-(trifluoromethyl)phenyl]-1,1-dioxo-2-propyl-N-[6-(trifluoromethyl)pyridin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-(4-methoxy-3-methylphenyl)-1,1-dioxo-2-propyl-N-[6-(trifluoromethyl)pyridin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-(3-chloro-4-methoxyphenyl)-1,1-dioxo-2-propyl-N-[6-(trifluoromethyl)pyridin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 2-(cyclopropylmethyl)-1,1-dioxo-5-[(1r,4r)-4-(trifluoromethyl)cyclohexyl]-N-[6-(trifluoromethyl)pyridin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-(3,4-dimethoxyphenyl)-1,1-dioxo-2-(prop-2-en-1-yl)-N-[6-(trifluoromethyl)pyridin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-(3,4-dimethoxyphenyl)-N-(4-methoxyphenyl)-1,1-dioxo-2-propyl-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-(3,4-dimethoxyphenyl)-N-(3-methylphenyl)-1,1-dioxo-2-propyl-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-[4-methoxy-3-(trifluoromethyl)phenyl]-1,1-dioxo-2-propyl-N-[3-(trifluoromethyl)phenyl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 5-(3,4-dimethoxyphenyl)-N-(6-fluoropyridin-2-yl)-1,1-dioxo-2-(propan-2-yl)-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; N-(6-fluoropyridin-2-yl)-1,1-dioxo-2-(propan-2-yl)-5-[(1r,4r)-4-(trifluoromethyl)cyclohexyl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 2-(cyclopropylmethyl)-N-(6-fluoropyrazin-2-yl)-1,1-dioxo-5-[(1r,4r)-4-(trifluoromethyl)cyclohexyl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 2-[(2R)-butan-2-yl]-5-(3,4-dimethoxyphenyl)-1,1-dioxo-N-[6-(trifluoromethyl)pyridin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 2-ethyl-5-[4-methoxy-3-(trifluoromethyl)phenyl]-1,1-dioxo-N-[6-(trifluoromethyl)pyridin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 1,1-dioxo-2-(propan-2-yl)-5-[(1r,4r)-4-(trifluoromethyl)cyclohexyl]-N-[6-(trifluoromethyl)pyrazin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 2-(cyclopropylmethyl)-5-(4,4-difluorocyclohexyl)-1,1-dioxo-N-[6-(trifluoromethyl)pyridin-2-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; 2-(cyclopropylmethyl)-1,1-dioxo-5-[(1r,4r)-4-(trifluoromethyl)cyclohexyl]-N-[2-(trifluoromethyl)pyrimidin-4-yl]-2H-1λ 6 ,2,6-thiadiazine-3-carboxamide; or pharmaceutically acceptable salts, biologically active metabolites, pro-drugs, racemates, enantiomers, diastereomers, solvates and hydrates thereof. 5 . A compound according to any one of claims 1 to 4 , for use in the treatment or prevention of a disease associated with α7 nicotinic acetylcholine receptor activity. 6 . A compound according to claim 5 , wherein the disease is selected from the group of psychotic disorders, including, but not limited to, schizophrenia, schizophreniform disorder, schizoaffective disorder, delusional disorder, brief psychotic disorder, psychotic disorder due to a general medical condition, substance-induced psychotic disorder or psychotic disorder not otherwise specified, cognitive impairment, including, but not limited to, cognitive impairment as a result of stroke, Alzheimer's disease, Huntington's disease, Pick disease, HIV associated dementia, frontotemporal dementia, Lewy body dementia, vascular dementia, cerebrovascular disease or other dementia states and dementia associated to other degenerative disorders, including, but not limited to, amyotrophic lateral sclerosis, other acute or sub-acute conditions that may cause cognitive decline, including, but not limited to, delirium, traumatic brain injury, senile dementia, mild cognitive impairment, Down's syndrome, depression and cognitive deficit related to other diseases, and dyskinetic disorders including, but not limited to, Parkinson's disease, neuroleptic-induced parkinsonism, or tardive dyskinesias, depression and mood disorders, including, but not limited to, depressive disorders and episodes, bipolar disorders, cyclothymic disorder, and bipolar disorder not otherwise specified, other mood disorders, substance-induced mood disorder and mood disorder not otherwise specified, anxiety disorders, panic disorder and panic attacks, obsessive compulsive disorder, posttraumatic stress disorder, acute stress disorder, generalized anxie

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Inventors

Classifications

  • A61K31/549Primary

    having two or more nitrogen atoms in the same ring, e.g. hydrochlorothiazide · CPC title

  • C07D417/04Primary

    directly linked by a ring-member-to-ring-member bond · CPC title

  • Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia · CPC title

  • Ortho-condensed systems · CPC title

  • Drugs for disorders of the nervous system · CPC title

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What does patent US2021267993A1 cover?
The invention relates to thiadiazine derivatives, or pharmaceutically acceptable salts, biologically active metabolites, pro-drugs, racemates, enantiomers, diastereomers, solvates and hydrates thereof, as well as to pharmaceutical compositions containing them and to their use as modulators of α7 nicotinic acetylcholine receptor activity in a mammalian subject Formula (I):
Who is the assignee on this patent?
Richter Gedeon Nyrt
What technology area does this patent fall under?
Primary CPC classification A61K31/549. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Sep 02 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). 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).