Kcnq2-5 channel activator
US-2017334855-A1 · Nov 23, 2017 · US
US9944618B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9944618-B2 |
| Application number | US-201414776397-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 10, 2014 |
| Priority date | Mar 14, 2013 |
| Publication date | Apr 17, 2018 |
| Grant date | Apr 17, 2018 |
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This document relates to compounds as well as methods and materials involved in modulating neurotransmitter reuptake. For example, compounds, methods for synthesizing compounds, and methods for inhibiting neurotransmitter reuptake are provided. Specifically gamma-amino alcohol derivatives that inhibit the reuptake of neurotransmitters such as dopamine, serotonin, epinephrine or norepinephrine are provided as therapeutic agents for the treatment of depression or anxiety in a mammalian subject.
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What is claimed is: 1. A compound of formula I: wherein R 1 is selected from naphthalen-2-yl, and phenyl substituted at the 3- or 4-position or 3- and 4-positions with a substituent selected from halogen and lower alkyl; R 2 is a 5- or 6-membered aromatic heterocycle each of which is substituted with substituents selected from halo, methylsulfanyl, methanesulfonyl, hydroxyl, methyl, ethyl, alkoxy, dimethylamino, and 1,1,1-trifluoromethanesulfonamide; optionally, two adjacent alkoxy groups are connected to form a 5- or 6-membered ring; R 3 is hydrogen, hydroxyl, lower alkoxy, or halo; and R 4 is hydrogen or lower alkyl. 2. The compound of claim 1 , wherein R 2 is substituted with one or two substituents. 3. The compound of claim 1 , having the formula Ia or Ib: wherein R a , R b , R c , R d , and R e are selected from hydrogen, lower alkyl, and halo. 4. The compound of claim 3 , wherein at least two of R a , R b , R c , R d , and R e are hydrogen. 5. The compound of claim 4 , wherein the remaining R a , R b , R c , R d , and R e are independently selected from ethyl, chloro, and bromo. 6. The compound of claim 3 , wherein R a , R d , and R e are hydrogen; and R b and R c are independently selected from ethyl, chloro, and bromo. 7. A compound of formula II: wherein R 2 is a 5- or 6-membered aromatic heterocycle each of which is substituted with substituents selected from halo, methylsulfanyl, methanesulfonyl, ethyl, alkoxy, dimethylamino, and 1,1,1-trifluoromethanesulfonamide; R 5 is hydrogen or lower alkyl; and R b and R c are independently hydrogen, halo, or lower alkyl. 8. The compound of claim 7 , wherein each of R b and R c is not hydrogen. 9. A compound of formula I: wherein R 1 is a phenyl substituted at the 3 or 4 position or 3- and 4-positions with a substituent selected from halogen and lower alkyl; R 2 is selected from phenyl and a 5- or 6-membered aromatic heterocycle each of which is optionally substituted with substituents selected from halo, methylsulfanyl, methanesulfonyl, hydroxyl, methyl, ethyl, alkoxy, dimethylamino, and 1,1,1-trifluoromethanesulfonamide; optionally, two adjacent alkoxy groups are connected to form a 5- or 6-membered ring; R 3 is hydrogen, hydroxyl, lower alkoxy, or halo; and R 4 is hydrogen or lower alkyl, wherein said compound has the formula Ia: wherein at least two of R a , R b , R c , R d , and R e are hydrogen, and wherein the remaining R a , R b , R c , R d , and R e are independently selected from ethyl, chloro, and bromo. 10. A compound of formula I: wherein R 1 is a phenyl substituted at the 3 or 4 position or 3- and 4-positions with a substituent selected from halogen and lower alkyl; R 2 is selected from phenyl and a 5- or 6-membered aromatic heterocycle each of which is optionally substituted with substituents selected from halo, methylsulfanyl, methanesulfonyl, hydroxyl, methyl, ethyl, alkoxy, dimethylamino, and 1,1,1-trifluoromethanesulfonamide; optionally, two adjacent alkoxy groups are connected to form a 5- or 6-membered ring; R 3 is hydrogen, hydroxyl, lower alkoxy, or halo; and R 4 is hydrogen or lower alkyl, wherein said compound has the formula Ia: wherein R a , R d , and R e are hydrogen; and R b and R c are independently selected from ethyl, chloro, and bromo.
having only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to the ring nitrogen atom · CPC title
having no double bonds between ring members or between ring members and non-ring members · CPC title
from aromatic carboxylic acids · CPC title
Halogen atoms · CPC title
having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring · CPC title
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