Novel 5-hydroxytryptamine receptor 7 activity modulators and their method of use

US2016016941A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016016941-A1
Application numberUS-201414774961-A
CountryUS
Kind codeA1
Filing dateMar 11, 2014
Priority dateMar 11, 2013
Publication dateJan 21, 2016
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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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Pharmaceutical compositions of the invention comprise functionalized lactone derivatives having a disease-modifying action in the treatment of diseases associated with dysregulation of 5-hydroxytryptamine receptor 7 activity.

First claim

Opening claim text (preview).

What is claimed is: 1 . A compound having formula (I): Including hydrates, solvates, pharmaceutically acceptable salts, prodrugs and complexes thereof, wherein: A is selected from a group consisting of R 1a and R 1b are independently selected from a group consisting of hydrogen, C 1-6 linear alkyl, C 1-6 branched alkyl, and optionally substituted aryl; R 1a and R 1b are taken together with the atom to which they are bound to form a ring having from 3 to 7 ring atoms; R 2a and R 2b are independently selected from a group consisting of hydrogen, C 1-6 linear alkyl, C 1-6 branched alkyl, and optionally substituted aryl; R 2a and R 2b are taken together with the atom to which they are bound to form a ring having from 3 to 7 ring atoms; R 3 is selected from a group consisting of C 1-6 linear alkyl, C 1-6 branched alkyl, C 3-7 cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, R 4 is optionally substituted aryl; R 5a and R 5b are each independently optionally substituted aryl; R 6a , R 6b , R 6c , and R 6d are each independently selected from a group consisting of hydrogen, halogen, OH, C 1-6 linear alkyl, C 1-6 branched alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, C 1-6 haloalkoxy, cyano, NH(C 1-6 alkyl), N(C 1-6 alkyl) 2 , NHC(O)R 7 , C(O)NHR 7 , C(O)N(R 7 ) 2 , SH, SC 1-6 alkyl, SO 2 NH 2 , SO 2 NHR 7 , SO 2 R 7 , and NHSO 2 R 7 ; R 7 is independently selected at each occurrence from a group consisting of C 1-6 linear alkyl, C 1-6 branched alkyl, and C 3-7 cycloalkyl; HetAr is optionally substituted heteroaryl; n is 1, 2, or 3; and m is 1 or 2. 2 . The compound of claim 1 , having the formula (XXXXII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 3 . The compound of claim 1 , having the formula (XXXXIII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 4 . The compound of claim 1 , having the formula (XXXXIV): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 5 . The compound of claim 1 , having the formula (XXXXV): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 6 . The compound of claim 1 , having the formula (XXXXV): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 7 . The compound of claim 1 , having the formula (XXXXVII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 8 . The compound of claim 1 , having the formula (XXXXVIII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 9 . The compound of claim 1 , having the formula (XXXXIX): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 10 . The compound of claim 1 , having the formula (XXXXX): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 11 . The compound of claim 1 , having the formula (XXXXXI): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 12 . The compound of claim 1 , having the formula (XXXXXII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 13 . The compound of claim 1 , having the formula (XXXXXIII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 14 . The compound of claim 1 , having the formula (XXXXXIV): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 15 . The compound of claim 1 , having the formula (XXXXXV): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 16 . The compound of claim 1 , having the formula (XXXXXVI): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 17 . The compound of claim 1 , having the formula (XXXXXVII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 18 . The compound of claim 1 , having the formula (XXXXXVIII): including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 19 . A compound of claim 1 , comprising: 2-(4-(2-(4,4-diethyl-5-oxotetrahydrofuran-2-yl)ethyl)piperazin-1-yl)benzonitrile; 3,3-diethyl-5-(2-(4-(4-methoxyphenyl)piperazin-1-yl)ethyl)dihydrofuran-2(3H)-one; 3,3-diethyl-5-(2-(4-(4-hydroxyphenyl)piperazin-1-yl)ethyl)dihydrofuran-2(3H)-one; 3,3-diethyl-5-(2-(4-(4-nitrophenyl)piperazin-1-yl)ethyl)dihydrofuran-2(3H)-one; 3,3-diethyl-5-(2-(4-(2-methoxyphenyl)piperazin-1-yl)eth

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Classifications

  • Antihypertensives · CPC title

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

  • Drugs for disorders of the metabolism (of the blood or the extracellular fluid A61P7/00) · CPC title

  • Antidepressants · CPC title

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What does patent US2016016941A1 cover?
Pharmaceutical compositions of the invention comprise functionalized lactone derivatives having a disease-modifying action in the treatment of diseases associated with dysregulation of 5-hydroxytryptamine receptor 7 activity.
Who is the assignee on this patent?
Univ Temple
What technology area does this patent fall under?
Primary CPC classification C07D405/12. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Jan 21 2016 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).